Item | Value |
---|---|
geneid | 29974 |
ensemblid | ENSG00000148584.16 |
hgncid | 24086 |
symbol | A1CF |
name | APOBEC1 complementation factor |
refseq_nuc | NM_014576.4 |
refseq_prot | NP_055391.2 |
ensembl_nuc | ENST00000373997.8 |
ensembl_prot | ENSP00000363109.3 |
mane_status | MANE Select |
chr | chr10 |
start | 50799409 |
end | 50885627 |
strand | - |
ver | v1.2 |
region | chr10:50799409-50885627 |
region5000 | chr10:50794409-50890627 |
regionname0 | A1CF_chr10_50799409_50885627 |
regionname5000 | A1CF_chr10_50794409_50890627 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 586 | 325 | 77 | 49 | 145 | 12 | 40 | A1CF_chr10_50794409_50890627 | A1CF | MESNH others(581): Show |
chr10 | 50794409 | 50890627 |
a0002 | 0/0 | 586 | 12 | 11 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | MESNH others(581): Show |
chr10 | 50794409 | 50890627 |
a0003 | 0/0 | 586 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | MESNH others(581): Show |
chr10 | 50794409 | 50890627 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1758 | 259 | 56 | 45 | 110 | 11 | 35 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0002 | 0/0 | 1758 | 35 | 10 | 1 | 19 | 0 | 5 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0003 | 0/0 | 1758 | 20 | 1 | 3 | 15 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0005 | 0/0 | 1758 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0007 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0008 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0009 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0011 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0001c0012 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0002c0004 | 0/0 | 1758 | 9 | 8 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0002c0006 | 0/0 | 1758 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 | ||
a0003c0010 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATGGA others(1753): Show |
chr10 | 50794409 | 50890627 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9215 | 79 | 16 | 18 | 33 | 6 | 6 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0002 | 0/0 | 9222 | 53 | 0 | 2 | 42 | 0 | 9 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0003 | 0/0 | 9222 | 45 | 1 | 12 | 23 | 3 | 6 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0005 | 1/0 | 9221 | 32 | 12 | 7 | 2 | 0 | 10 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0007 | 0/0 | 9214 | 3 | 1 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9209): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0008 | 0/0 | 9221 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0009 | 0/0 | 9221 | 4 | 4 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0010 | 0/0 | 9221 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0011 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0012 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0014 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0015 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0016 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0017 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0019 | 0/0 | 9220 | 2 | 1 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9215): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0020 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0021 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0022 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0023 | 0/0 | 9215 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0025 | 0/0 | 9216 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9211): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0026 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0027 | 0/1 | 9215 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0028 | 0/0 | 9215 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0029 | 0/0 | 9221 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0030 | 0/0 | 9223 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9218): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0031 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0032 | 0/0 | 9222 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0033 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0036 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0037 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0038 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0039 | 0/0 | 9221 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0040 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0041 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0042 | 0/0 | 9222 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0043 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0046 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0001t0049 | 0/0 | 9221 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0002t0004 | 0/0 | 9221 | 33 | 10 | 1 | 19 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0002t0013 | 0/0 | 9222 | 2 | 0 | 0 | 0 | 0 | 2 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0003t0001 | 0/0 | 9215 | 17 | 1 | 3 | 12 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0003t0007 | 0/0 | 9214 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9209): Show |
chr10 | 50794409 | 50890627 |
a0001c0003t0047 | 0/0 | 9214 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9209): Show |
chr10 | 50794409 | 50890627 |
a0001c0005t0001 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0005t0024 | 0/0 | 9216 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9211): Show |
chr10 | 50794409 | 50890627 |
a0001c0005t0048 | 0/0 | 9214 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9209): Show |
chr10 | 50794409 | 50890627 |
a0001c0007t0005 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0007t0034 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0008t0001 | 0/0 | 9215 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
a0001c0008t0017 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0009t0004 | 0/0 | 9221 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0001c0011t0002 | 0/0 | 9222 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0001c0012t0035 | 0/0 | 9221 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9216): Show |
chr10 | 50794409 | 50890627 |
a0002c0004t0006 | 0/0 | 9222 | 5 | 4 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0002c0004t0018 | 0/0 | 9222 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0002c0004t0044 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0002c0004t0045 | 0/0 | 9222 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0002c0006t0006 | 0/0 | 9222 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9217): Show |
chr10 | 50794409 | 50890627 |
a0003c0010t0001 | 0/0 | 9215 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | ATAAT others(9210): Show |
chr10 | 50794409 | 50890627 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0004 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0008g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0010g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0014g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0017g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0019g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0021g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0022g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0023g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0025g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0026g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0027g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0028g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0029g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0030g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0031g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0032g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0036g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0037g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0038g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0039g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0040g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0041g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0042g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0043g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0046g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0001t0049g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0013g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0002t0013g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0003t0047g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0005t0048g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0007t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0007t0034g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0008t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0008t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0009t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0009t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0011t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0001c0012t0035g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0044g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0004t0045g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0002c0006t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
a0003c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0032 | g0059 | EUR | GBR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0159 | EUR | FIN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00423 | hp1 | a0001 | c0001 | t0033 | g0064 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0078 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00639 | hp1 | a0002 | c0004 | t0006 | g0260 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0257 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01069 | hp2 | a0001 | c0001 | t0029 | g0058 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01192 | hp1 | a0001 | c0001 | t0010 | g0101 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0090 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0239 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0259 | AMR | PUR | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01257 | hp1 | a0001 | c0001 | t0021 | g0115 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01361 | hp2 | a0001 | c0001 | t0023 | g0119 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01516 | hp2 | a0001 | c0001 | t0022 | g0266 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0161 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01891 | hp2 | a0001 | c0001 | t0043 | g0098 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0010 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01981 | hp2 | a0001 | c0001 | t0042 | g0043 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02015 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0163 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02055 | hp2 | a0002 | c0004 | t0006 | g0037 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02080 | hp2 | a0001 | c0001 | t0025 | g0125 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0075 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02145 | hp1 | a0002 | c0004 | t0006 | g0210 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02145 | hp2 | a0001 | c0001 | t0016 | g0046 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CDX | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | CDX | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02257 | hp1 | a0001 | c0001 | t0017 | g0262 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02258 | hp2 | a0001 | c0007 | t0005 | g0242 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0271 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0252 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0222 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02451 | hp2 | a0002 | c0006 | t0006 | g0053 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0084 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0265 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02615 | hp1 | a0002 | c0004 | t0045 | g0199 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02622 | hp1 | a0002 | c0004 | t0006 | g0225 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0146 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02717 | hp1 | a0001 | c0005 | t0048 | g0207 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02723 | hp2 | a0001 | c0001 | t0019 | g0240 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02735 | hp1 | a0001 | c0002 | t0004 | g0085 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02738 | hp2 | a0001 | c0002 | t0013 | g0092 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02886 | hp2 | a0002 | c0004 | t0018 | g0040 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02895 | hp1 | a0001 | c0009 | t0004 | g0251 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02897 | hp1 | a0001 | c0009 | t0004 | g0250 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02897 | hp2 | a0001 | c0008 | t0001 | g0045 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02922 | hp2 | a0001 | c0001 | t0038 | g0056 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0097 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02976 | hp1 | a0001 | c0001 | t0040 | g0044 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02976 | hp2 | a0001 | c0001 | t0011 | g0096 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0245 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03139 | hp2 | a0001 | c0002 | t0004 | g0042 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0248 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03225 | hp2 | a0001 | c0012 | t0035 | g0157 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03453 | hp2 | a0001 | c0005 | t0001 | g0205 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0249 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03516 | hp2 | a0001 | c0007 | t0034 | g0243 | AFR | ESN | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0100 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03540 | hp2 | a0002 | c0004 | t0018 | g0156 | AFR | GWD | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03579 | hp2 | a0002 | c0004 | t0006 | g0037 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0272 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03654 | hp2 | a0001 | c0002 | t0013 | g0089 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03669 | hp1 | a0001 | c0001 | t0028 | g0088 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0256 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03710 | hp1 | a0001 | c0001 | t0039 | g0171 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0086 | SAS | PJL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03831 | hp1 | a0001 | c0001 | t0030 | g0063 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0274 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0270 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03927 | hp2 | a0001 | c0001 | t0026 | g0060 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0273 | SAS | BEB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0267 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0147 | SAS | STU | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18906 | hp1 | a0001 | c0008 | t0017 | g0049 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18906 | hp2 | a0002 | c0006 | t0006 | g0051 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18939 | hp2 | a0001 | c0003 | t0047 | g0218 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18946 | hp2 | a0001 | c0011 | t0002 | g0186 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18950 | hp2 | a0001 | c0001 | t0031 | g0228 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18970 | hp2 | a0003 | c0010 | t0001 | g0139 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18974 | hp2 | a0001 | c0003 | t0007 | g0230 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18977 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18984 | hp1 | a0001 | c0001 | t0037 | g0184 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18991 | hp1 | a0001 | c0001 | t0049 | g0170 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19004 | hp2 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19011 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19012 | hp1 | a0001 | c0001 | t0046 | g0126 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0247 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19060 | hp2 | a0001 | c0002 | t0004 | g0110 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19065 | hp2 | a0001 | c0001 | t0020 | g0117 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19070 | hp1 | a0001 | c0003 | t0007 | g0231 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19072 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19074 | hp2 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19076 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19077 | hp2 | a0001 | c0001 | t0036 | g0158 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19083 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19091 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA19240 | hp2 | a0002 | c0006 | t0006 | g0052 | AFR | YRI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20129 | hp1 | a0002 | c0004 | t0044 | g0055 | AFR | ASW | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | GIH | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0091 | SAS | GIH | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02559 | hp1 | a0001 | c0005 | t0024 | g0206 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG02559 | hp2 | a0001 | c0001 | t0015 | g0099 | AFR | ACB | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03471 | hp1 | a0001 | c0001 | t0041 | g0054 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | MSL | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18955 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0104 | REF | REF | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0047 | REF | REF | A1CF_chr10_50794409_50890627 | A1CF | chr10 | 50794409 | 50890627 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50806851 | C | T | 1 | a0002 | 12 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
missense_variant | MODERATE | c.1639G>A | p.Val547Met | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1779/9221 | 1639/1761 | 547/586 | chr10 | 50806851 | |||
chr10:50811146 | A | G | 1 | a0003 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.1354T>C | p.Trp452Arg | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/13 | 1494/9221 | 1354/1761 | 452/586 | chr10 | 50811146 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50806834 | G | C | 1 | a0001c0003 | 20 | HG00280.hp2 HG00558.hp2 HG01346.hp1 others(17): Show |
synonymous_variant | LOW | c.1656C>G | p.Leu552Leu | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1796/9221 | 1656/1761 | 552/586 | chr10 | 50806834 | |||
chr10:50809991 | C | T | 1 | a0001c0009 | 2 | HG02895.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.1512G>A | p.Thr504Thr | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/13 | 1652/9221 | 1512/1761 | 504/586 | chr10 | 50809991 | |||
chr10:50813938 | G | A | 3 | a0001c0002a0001c0009a0001c0012 | 38 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
synonymous_variant | LOW | c.1242C>T | p.Leu414Leu | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/13 | 1382/9221 | 1242/1761 | 414/586 | chr10 | 50813938 | |||
chr10:50816244 | T | G | 1 | a0001c0011 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.903A>C | p.Ala301Ala | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/13 | 1043/9221 | 903/1761 | 301/586 | chr10 | 50816244 | |||
chr10:50836093 | C | T | 2 | a0001c0008a0002c0006 | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
synonymous_variant | LOW | c.585G>A | p.Ala195Ala | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 725/9221 | 585/1761 | 195/586 | chr10 | 50836093 | |||
chr10:50836150 | G | T | 1 | a0001c0007 | 2 | HG02258.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.528C>A | p.Thr176Thr | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 668/9221 | 528/1761 | 176/586 | chr10 | 50836150 | |||
chr10:50836216 | C | T | 1 | a0001c0005 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.462G>A | p.Ser154Ser | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/13 | 602/9221 | 462/1761 | 154/586 | chr10 | 50836216 | |||
chr10:50859911 | T | G | 1 | a0001c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.30A>C | p.Gly10Gly | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/13 | 170/9221 | 30/1761 | 10/586 | chr10 | 50859911 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50799749 | G | C | 1 | a0001c0001t0026 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6980C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6980 | chr10 | 50799749 | ||||||
chr10:50799836 | C | T | 2 | a0001c0005t0024a0001c0005t0048 | 2 | HG02559.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6893G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6893 | chr10 | 50799836 | ||||||
chr10:50799874 | A | G | 12 | a0001c0001t0016a0001c0001t0017a0001c0002t0004others(9): Show | 54 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*6855T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6855 | chr10 | 50799874 | ||||||
chr10:50800042 | A | G | 1 | a0001c0001t0032 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6687T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6687 | chr10 | 50800042 | ||||||
chr10:50800083 | T | G | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*6646A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6646 | chr10 | 50800083 | ||||||
chr10:50800104 | A | T | 1 | a0001c0003t0047 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6625T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6625 | chr10 | 50800104 | ||||||
chr10:50800240 | C | T | 1 | a0001c0001t0019 | 2 | HG01243.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6489G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6489 | chr10 | 50800240 | ||||||
chr10:50800634 | G | A | 4 | a0001c0001t0038a0001c0001t0040a0001c0001t0041others(1): Show | 4 | HG01981.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6095C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6095 | chr10 | 50800634 | ||||||
chr10:50800716 | G | A | 5 | a0001c0001t0002a0001c0001t0036a0001c0001t0037others(2): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*6013C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 6013 | chr10 | 50800716 | ||||||
chr10:50800797 | G | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*5932C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5932 | chr10 | 50800797 | ||||||
chr10:50800898 | A | T | 6 | a0001c0001t0016a0002c0004t0006a0002c0004t0018others(3): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5831T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5831 | chr10 | 50800898 | ||||||
chr10:50800933 | C | T | 1 | a0002c0004t0018 | 2 | HG02886.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5796G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5796 | chr10 | 50800933 | ||||||
chr10:50800934 | G | A | 1 | a0001c0001t0011 | 2 | HG02965.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5795C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5795 | chr10 | 50800934 | ||||||
chr10:50800971 | T | A | 1 | a0001c0001t0038 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5758A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5758 | chr10 | 50800971 | ||||||
chr10:50801395 | T | A | 7 | a0001c0001t0017a0001c0008t0017a0002c0004t0006others(4): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5334A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5334 | chr10 | 50801395 | ||||||
chr10:50801491 | G | A | 1 | a0001c0001t0042 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5238C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 5238 | chr10 | 50801491 | ||||||
chr10:50801883 | T | C | 3 | a0001c0001t0012a0001c0001t0029a0001c0007t0034 | 4 | HG01069.hp2 HG02451.hp1 HG02572.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4846A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4846 | chr10 | 50801883 | ||||||
chr10:50802039 | G | A | 1 | a0002c0004t0045 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4690C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4690 | chr10 | 50802039 | ||||||
chr10:50802043 | A | G | 5 | a0001c0001t0016a0001c0002t0004a0001c0002t0013others(2): Show | 40 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4686T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4686 | chr10 | 50802043 | ||||||
chr10:50802069 | C | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*4660G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4660 | chr10 | 50802069 | ||||||
chr10:50802159 | C | T | 5 | a0001c0001t0002a0001c0001t0036a0001c0001t0037others(2): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4570 | chr10 | 50802159 | ||||||
chr10:50802194 | C | T | 1 | a0001c0001t0008 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4535G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4535 | chr10 | 50802194 | ||||||
chr10:50802340 | G | A | 1 | a0001c0001t0010 | 3 | HG01192.hp1 HG02630.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4389C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4389 | chr10 | 50802340 | ||||||
chr10:50802678 | CTTAGTG | C | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*4045_*4050delCACT others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 4045 | chr10 | 50802678 | ||||||
chr10:50803237 | C | T | 1 | a0001c0001t0031 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3492G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3492 | chr10 | 50803237 | ||||||
chr10:50803269 | G | GT | 16 | a0001c0001t0014a0001c0001t0017a0001c0001t0025others(13): Show | 25 | HG00639.hp1 HG01981.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3459dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3459 | chr10 | 50803269 | ||||||
chr10:50803269 | G | T | 1 | a0001c0001t0023 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3460C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3460 | chr10 | 50803269 | ||||||
chr10:50803291 | C | T | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(8): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3438G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3438 | chr10 | 50803291 | ||||||
chr10:50803387 | G | A | 1 | a0001c0001t0028 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3342C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3342 | chr10 | 50803387 | ||||||
chr10:50803391 | C | T | 2 | a0001c0001t0038a0001c0001t0040 | 2 | HG02922.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3338G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3338 | chr10 | 50803391 | ||||||
chr10:50803436 | A | G | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3293T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3293 | chr10 | 50803436 | ||||||
chr10:50803585 | A | C | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3144T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3144 | chr10 | 50803585 | ||||||
chr10:50803619 | A | G | 2 | a0001c0001t0029a0001c0007t0034 | 2 | HG01069.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3110T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 3110 | chr10 | 50803619 | ||||||
chr10:50803947 | A | G | 1 | a0001c0001t0022 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2782T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2782 | chr10 | 50803947 | ||||||
chr10:50803965 | G | A | 1 | a0001c0001t0033 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2764C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2764 | chr10 | 50803965 | ||||||
chr10:50804022 | G | A | 1 | a0001c0001t0009 | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2707C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2707 | chr10 | 50804022 | ||||||
chr10:50804305 | C | T | 1 | a0001c0001t0021 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2424G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2424 | chr10 | 50804305 | ||||||
chr10:50804315 | A | AT | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(8): Show | 108 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2413dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2413 | chr10 | 50804315 | ||||||
chr10:50804519 | C | T | 1 | a0001c0001t0039 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2210G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2210 | chr10 | 50804519 | ||||||
chr10:50804661 | G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*2068C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 2068 | chr10 | 50804661 | ||||||
chr10:50804764 | G | T | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1965C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1965 | chr10 | 50804764 | ||||||
chr10:50804865 | A | T | 1 | a0001c0001t0038 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1864T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1864 | chr10 | 50804865 | ||||||
chr10:50805008 | G | A | 3 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1721 | chr10 | 50805008 | ||||||
chr10:50805422 | C | T | 1 | a0002c0004t0044 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1307 | chr10 | 50805422 | ||||||
chr10:50805438 | G | A | 1 | a0001c0001t0036 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1291 | chr10 | 50805438 | ||||||
chr10:50805472 | T | C | 1 | a0001c0001t0037 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1257 | chr10 | 50805472 | ||||||
chr10:50805613 | C | T | 1 | a0001c0001t0020 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1116G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 1116 | chr10 | 50805613 | ||||||
chr10:50805968 | G | T | 1 | a0001c0001t0029 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*761C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 761 | chr10 | 50805968 | ||||||
chr10:50806119 | G | C | 2 | a0001c0001t0009a0001c0001t0043 | 5 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 610 | chr10 | 50806119 | ||||||
chr10:50806180 | A | C | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 549 | chr10 | 50806180 | ||||||
chr10:50806289 | T | C | 8 | a0001c0001t0016a0001c0001t0017a0001c0008t0017others(5): Show | 16 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*440A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 440 | chr10 | 50806289 | ||||||
chr10:50806297 | A | G | 18 | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*432T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 432 | chr10 | 50806297 | ||||||
chr10:50806607 | G | A | 1 | a0001c0001t0046 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 122 | chr10 | 50806607 | ||||||
chr10:50806672 | CT | C | 6 | a0001c0001t0007a0001c0001t0019a0001c0001t0049others(3): Show | 10 | HG01243.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*56delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 13/13 | 56 | chr10 | 50806672 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:50807085 | C | T | 1 | a0001c0001t0003g0017 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1610-205G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807085 | |||||||
chr10:50807215 | G | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(245): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1610-335C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807215 | |||||||
chr10:50807300 | G | A | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1610-420C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807300 | |||||||
chr10:50807411 | G | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0008t0001g0045 | 3 | HG02109.hp1 HG02486.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1610-531C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807411 | |||||||
chr10:50807564 | G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0008t0001g0045 | 3 | HG02109.hp1 HG02486.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1610-684C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807564 | |||||||
chr10:50807672 | G | A | 1 | a0001c0001t0005g0274 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1610-792C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50807672 | |||||||
chr10:50808105 | A | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(233): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1610-1225T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808105 | |||||||
chr10:50808118 | T | C | 1 | a0002c0004t0006g0260 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1610-1238A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808118 | |||||||
chr10:50808246 | C | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1610-1366G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808246 | |||||||
chr10:50808856 | T | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(231): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1609+1038A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50808856 | |||||||
chr10:50809127 | G | T | 7 | a0001c0001t0005g0203a0001c0001t0005g0204a0001c0001t0005g0212others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+767C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809127 | |||||||
chr10:50809238 | A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1609+656T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809238 | |||||||
chr10:50809321 | C | G | 1 | a0001c0001t0002g0178 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1609+573G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809321 | |||||||
chr10:50809332 | C | A | 6 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1609+562G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809332 | |||||||
chr10:50809791 | C | T | 1 | a0001c0001t0008g0006 | 3 | HG02258.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1609+103G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809791 | |||||||
chr10:50809877 | G | A | 34 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0014others(31): Show | 46 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1609+17C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 12/12 | chr10 | 50809877 | |||||||
chr10:50810338 | C | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(92): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1461-296G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810338 | |||||||
chr10:50810355 | G | C | 85 | a0001c0001t0001g0118a0001c0001t0002g0001a0001c0001t0002g0007others(82): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1461-313C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810355 | |||||||
chr10:50810457 | A | G | 30 | a0001c0002t0004g0002a0001c0002t0004g0020a0001c0002t0004g0021others(27): Show | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1461-415T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810457 | |||||||
chr10:50810463 | G | A | 2 | a0001c0001t0005g0146a0001c0001t0005g0147 | 2 | HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1461-421C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810463 | |||||||
chr10:50810481 | G | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(92): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1461-439C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810481 | |||||||
chr10:50810503 | A | G | 2 | a0001c0001t0029g0058a0001c0007t0034g0243 | 2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1461-461T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810503 | |||||||
chr10:50810578 | G | A | 1 | a0001c0007t0034g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1460+462C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810578 | |||||||
chr10:50810620 | G | A | 3 | a0001c0002t0004g0163a0001c0003t0001g0114a0001c0003t0001g0221 | 3 | HG02055.hp1 NA18945.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1460+420C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810620 | |||||||
chr10:50810881 | C | T | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1460+159G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810881 | |||||||
chr10:50810983 | T | G | 7 | a0002c0004t0006g0037a0002c0004t0006g0210a0002c0004t0006g0225others(4): Show | 8 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+57A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | 50810983 | |||||||
chr10:50811298 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1324-122T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811298 | |||||||
chr10:50811304 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1324-128A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811304 | |||||||
chr10:50811405 | T | C | 1 | a0001c0001t0005g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1324-229A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811405 | |||||||
chr10:50811485 | A | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(85): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1324-309T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811485 | |||||||
chr10:50811532 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1324-356G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811532 | |||||||
chr10:50811600 | C | T | 6 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-424G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811600 | |||||||
chr10:50811613 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1324-437T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811613 | |||||||
chr10:50811668 | G | C | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1324-492C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811668 | |||||||
chr10:50811742 | C | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(245): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1324-566G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811742 | |||||||
chr10:50811909 | T | G | 1 | a0001c0001t0042g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1324-733A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811909 | |||||||
chr10:50811941 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1324-765T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811941 | |||||||
chr10:50811954 | G | A | 1 | a0001c0003t0007g0231 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1324-778C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811954 | |||||||
chr10:50811969 | T | C | 6 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-793A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50811969 | |||||||
chr10:50812043 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1324-867T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812043 | |||||||
chr10:50812164 | T | C | 85 | a0001c0001t0001g0118a0001c0001t0002g0001a0001c0001t0002g0007others(82): Show | 109 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1324-988A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812164 | |||||||
chr10:50812251 | G | A | 1 | a0001c0001t0033g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1324-1075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812251 | |||||||
chr10:50812341 | C | T | 1 | a0001c0002t0004g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1324-1165G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812341 | |||||||
chr10:50812359 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1324-1183C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812359 | |||||||
chr10:50812526 | C | T | 6 | a0001c0001t0017g0262a0001c0001t0038g0056a0001c0001t0040g0044others(3): Show | 6 | HG01981.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1331G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812526 | |||||||
chr10:50812613 | T | C | 1 | a0001c0001t0043g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1323+1244A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812613 | |||||||
chr10:50812749 | C | T | 30 | a0001c0002t0004g0002a0001c0002t0004g0020a0001c0002t0004g0021others(27): Show | 37 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1323+1108G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812749 | |||||||
chr10:50812880 | T | A | 4 | a0001c0001t0001g0094a0001c0001t0017g0262a0001c0001t0041g0054others(1): Show | 4 | HG02257.hp1 HG03471.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+977A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812880 | |||||||
chr10:50812893 | G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1323+964C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812893 | |||||||
chr10:50812964 | A | C | 2 | a0001c0001t0012g0084a0001c0001t0012g0222 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1323+893T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812964 | |||||||
chr10:50812976 | C | T | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+881G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812976 | |||||||
chr10:50812981 | A | G | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1323+876T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50812981 | |||||||
chr10:50813273 | A | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0103a0001c0001t0001g0150others(2): Show | 6 | NA18947.hp2 NA18962.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+584T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813273 | |||||||
chr10:50813499 | C | A | 8 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1323+358G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813499 | |||||||
chr10:50813654 | A | T | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1323+203T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | 50813654 | |||||||
chr10:50814086 | A | G | 1 | a0001c0001t0005g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1142-48T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814086 | |||||||
chr10:50814156 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1142-118A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814156 | |||||||
chr10:50814208 | C | T | 1 | a0001c0001t0009g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1142-170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814208 | |||||||
chr10:50814276 | C | T | 1 | a0001c0003t0001g0140 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1142-238G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814276 | |||||||
chr10:50814313 | C | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(85): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1142-275G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814313 | |||||||
chr10:50814344 | A | G | 12 | a0001c0001t0002g0029a0001c0001t0002g0173a0001c0001t0002g0178others(9): Show | 13 | HG00438.hp2 HG00558.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1142-306T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814344 | |||||||
chr10:50814707 | A | G | 1 | a0001c0001t0033g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1142-669T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814707 | |||||||
chr10:50814885 | A | G | 50 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(47): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1142-847T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50814885 | |||||||
chr10:50815113 | G | T | 1 | a0001c0001t0003g0261 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1141+893C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815113 | |||||||
chr10:50815133 | C | T | 3 | a0001c0001t0017g0262a0001c0001t0041g0054a0001c0008t0017g0049 | 3 | HG02257.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1141+873G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815133 | |||||||
chr10:50815394 | T | C | 2 | a0001c0001t0005g0146a0001c0001t0005g0147 | 2 | HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1141+612A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815394 | |||||||
chr10:50815521 | T | A | 1 | a0001c0001t0003g0130 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1141+485A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815521 | |||||||
chr10:50815728 | T | C | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141+278A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815728 | |||||||
chr10:50815888 | A | G | 1 | a0001c0003t0001g0217 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1141+118T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815888 | |||||||
chr10:50815930 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1141+76T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | 50815930 | |||||||
chr10:50816307 | C | T | 1 | a0001c0001t0005g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.868-28G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816307 | |||||||
chr10:50816308 | G | A | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(234): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.868-29C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816308 | |||||||
chr10:50816354 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.868-75A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816354 | |||||||
chr10:50816459 | G | A | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.868-180C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816459 | |||||||
chr10:50816670 | A | G | 34 | a0001c0001t0005g0011a0001c0001t0016g0046a0001c0001t0016g0048others(31): Show | 43 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.868-391T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816670 | |||||||
chr10:50816728 | T | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(93): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.868-449A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816728 | |||||||
chr10:50816782 | C | T | 4 | a0001c0001t0005g0112a0001c0001t0005g0254a0001c0001t0005g0265others(1): Show | 4 | HG00438.hp1 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-503G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816782 | |||||||
chr10:50816830 | T | C | 13 | a0001c0001t0017g0262a0001c0008t0017g0049a0002c0004t0006g0037others(10): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-551A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50816830 | |||||||
chr10:50817113 | G | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(85): Show | 112 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.868-834C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817113 | |||||||
chr10:50817296 | A | C | 1 | a0001c0001t0002g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.868-1017T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817296 | |||||||
chr10:50817493 | G | A | 13 | a0001c0001t0017g0262a0001c0008t0017g0049a0002c0004t0006g0037others(10): Show | 14 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.868-1214C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817493 | |||||||
chr10:50817596 | G | A | 8 | a0002c0004t0006g0037a0002c0004t0006g0210a0002c0004t0006g0225others(5): Show | 9 | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-1317C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50817596 | |||||||
chr10:50818055 | C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(91): Show | 113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.868-1776G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818055 | |||||||
chr10:50818191 | C | T | 2 | a0001c0001t0016g0046a0001c0001t0016g0048 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.868-1912G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818191 | |||||||
chr10:50818220 | G | C | 1 | a0001c0007t0034g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.868-1941C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818220 | |||||||
chr10:50818352 | T | A | 88 | a0001c0001t0001g0118a0001c0001t0002g0001a0001c0001t0002g0007others(85): Show | 112 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.868-2073A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818352 | |||||||
chr10:50818440 | A | G | 1 | a0001c0001t0041g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+2112T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818440 | |||||||
chr10:50818518 | C | T | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(263): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.867+2034G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818518 | |||||||
chr10:50818612 | C | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0215 | 2 | NA18987.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.867+1940G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818612 | |||||||
chr10:50818711 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.867+1841C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818711 | |||||||
chr10:50818804 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.867+1748G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818804 | |||||||
chr10:50818956 | C | G | 2 | a0001c0001t0029g0058a0001c0007t0034g0243 | 2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.867+1596G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818956 | |||||||
chr10:50818978 | A | G | 63 | a0001c0001t0001g0143a0001c0001t0002g0057a0001c0001t0002g0165others(60): Show | 77 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.867+1574T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50818978 | |||||||
chr10:50819061 | G | C | 4 | a0001c0001t0019g0239a0001c0001t0019g0240a0001c0001t0042g0043others(1): Show | 4 | HG01243.hp1 HG01981.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+1491C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819061 | |||||||
chr10:50819137 | T | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1415A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819137 | |||||||
chr10:50819158 | C | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0133others(1): Show | 4 | HG01167.hp2 HG02109.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+1394G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819158 | |||||||
chr10:50819250 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1302C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819250 | |||||||
chr10:50819291 | C | T | 1 | a0001c0001t0041g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+1261G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819291 | |||||||
chr10:50819292 | G | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(55): Show | 68 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.867+1260C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819292 | |||||||
chr10:50819457 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.867+1095G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819457 | |||||||
chr10:50819491 | C | T | 2 | a0001c0001t0015g0099a0001c0001t0015g0100 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.867+1061G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819491 | |||||||
chr10:50819494 | T | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0208a0001c0001t0001g0211others(2): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.867+1058A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819494 | |||||||
chr10:50819551 | C | T | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.867+1001G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819551 | |||||||
chr10:50819566 | G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+986C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819566 | |||||||
chr10:50819654 | A | G | 2 | a0001c0001t0001g0136a0001c0001t0028g0088 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.867+898T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819654 | |||||||
chr10:50819781 | G | C | 1 | a0001c0008t0017g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.867+771C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819781 | |||||||
chr10:50819835 | T | C | 7 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.867+717A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819835 | |||||||
chr10:50819943 | C | A | 9 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+609G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819943 | |||||||
chr10:50819990 | T | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+562A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50819990 | |||||||
chr10:50820208 | C | T | 1 | a0002c0006t0006g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.867+344G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50820208 | |||||||
chr10:50820453 | G | A | 5 | a0001c0008t0001g0045a0002c0004t0044g0055a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+99C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | 50820453 | |||||||
chr10:50820692 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.770-43C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820692 | |||||||
chr10:50820797 | A | G | 9 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-148T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820797 | |||||||
chr10:50820889 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.770-240C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820889 | |||||||
chr10:50820933 | T | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.770-284A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50820933 | |||||||
chr10:50821359 | C | T | 9 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-710G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821359 | |||||||
chr10:50821442 | A | G | 1 | a0001c0001t0040g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.770-793T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821442 | |||||||
chr10:50821535 | A | C | 1 | a0001c0001t0002g0179 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.770-886T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821535 | |||||||
chr10:50821541 | A | AT | 125 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(122): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.770-893dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821541 | |||||||
chr10:50821757 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.770-1108C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821757 | |||||||
chr10:50821807 | G | C | 4 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-1158C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821807 | |||||||
chr10:50821966 | T | G | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.770-1317A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50821966 | |||||||
chr10:50822075 | C | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-1426G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822075 | |||||||
chr10:50822105 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.770-1456A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822105 | |||||||
chr10:50822132 | A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0191a0001c0001t0001g0233others(2): Show | 9 | HG00738.hp1 HG01258.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-1483T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822132 | |||||||
chr10:50822370 | G | A | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-1721C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822370 | |||||||
chr10:50822465 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.770-1816C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822465 | |||||||
chr10:50822497 | C | T | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-1848G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822497 | |||||||
chr10:50822500 | G | A | 1 | a0001c0001t0015g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.770-1851C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822500 | |||||||
chr10:50822594 | T | G | 1 | a0001c0001t0002g0009 | 3 | HG02083.hp1 NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.770-1945A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822594 | |||||||
chr10:50822746 | A | T | 1 | a0001c0007t0034g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.770-2097T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822746 | |||||||
chr10:50822756 | G | A | 1 | a0001c0001t0016g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.770-2107C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822756 | |||||||
chr10:50822778 | C | T | 1 | a0001c0001t0022g0266 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.770-2129G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822778 | |||||||
chr10:50822817 | C | T | 1 | a0001c0001t0011g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.770-2168G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822817 | |||||||
chr10:50822826 | A | C | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-2177T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822826 | |||||||
chr10:50822855 | C | T | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.770-2206G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822855 | |||||||
chr10:50822885 | C | A | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.770-2236G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50822885 | |||||||
chr10:50823008 | G | A | 1 | a0001c0001t0021g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.770-2359C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823008 | |||||||
chr10:50823283 | G | A | 19 | a0001c0001t0001g0219a0001c0001t0031g0228a0001c0003t0001g0010others(16): Show | 22 | HG00280.hp2 HG00558.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-2634C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823283 | |||||||
chr10:50823490 | C | A | 1 | a0001c0002t0004g0020 | 2 | NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.770-2841G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823490 | |||||||
chr10:50823533 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.770-2884G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823533 | |||||||
chr10:50823534 | G | C | 21 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(18): Show | 24 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.770-2885C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823534 | |||||||
chr10:50823648 | G | A | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-2999C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823648 | |||||||
chr10:50823735 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-3086T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823735 | |||||||
chr10:50823863 | G | A | 2 | a0002c0004t0006g0210a0002c0004t0006g0225 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.770-3214C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823863 | |||||||
chr10:50823903 | G | A | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3254C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823903 | |||||||
chr10:50823968 | C | G | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-3319G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50823968 | |||||||
chr10:50824153 | G | A | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.770-3504C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824153 | |||||||
chr10:50824284 | C | T | 1 | a0001c0001t0033g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.770-3635G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824284 | |||||||
chr10:50824285 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.770-3636C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824285 | |||||||
chr10:50824350 | T | C | 47 | a0001c0001t0001g0268a0001c0001t0003g0008a0001c0001t0003g0019others(44): Show | 60 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.770-3701A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824350 | |||||||
chr10:50824412 | G | T | 1 | a0001c0001t0015g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.769+3719C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824412 | |||||||
chr10:50824645 | GGCATGTA others(3): Show |
G | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+3476_769+3485d others(12): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824645 | |||||||
chr10:50824709 | C | T | 1 | a0001c0003t0001g0140 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.769+3422G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824709 | |||||||
chr10:50824917 | C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+3214G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824917 | |||||||
chr10:50824949 | C | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+3182G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50824949 | |||||||
chr10:50825233 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.769+2898G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825233 | |||||||
chr10:50825450 | T | A | 1 | a0001c0001t0003g0014 | 2 | NA18945.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.769+2681A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825450 | |||||||
chr10:50825453 | G | A | 5 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+2678C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825453 | |||||||
chr10:50825479 | A | G | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769+2652T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50825479 | |||||||
chr10:50826129 | T | C | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+2002A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826129 | |||||||
chr10:50826428 | A | G | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.769+1703T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826428 | |||||||
chr10:50826446 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.769+1685C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826446 | |||||||
chr10:50826480 | C | T | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+1651G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826480 | |||||||
chr10:50826533 | G | C | 7 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+1598C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826533 | |||||||
chr10:50826560 | A | G | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.769+1571T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826560 | |||||||
chr10:50826579 | T | G | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.769+1552A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826579 | |||||||
chr10:50826860 | T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(265): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.769+1271A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826860 | |||||||
chr10:50826869 | C | T | 1 | a0001c0002t0004g0081 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.769+1262G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826869 | |||||||
chr10:50826910 | T | C | 1 | a0001c0001t0005g0256 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+1221A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50826910 | |||||||
chr10:50827088 | C | A | 1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.769+1043G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827088 | |||||||
chr10:50827313 | A | G | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+818T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827313 | |||||||
chr10:50827410 | G | T | 1 | a0001c0002t0004g0110 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.769+721C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827410 | |||||||
chr10:50827485 | C | A | 21 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(18): Show | 24 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.769+646G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827485 | |||||||
chr10:50827506 | A | T | 2 | a0001c0001t0003g0065a0001c0001t0003g0067 | 2 | HG02074.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.769+625T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827506 | |||||||
chr10:50827812 | G | T | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.769+319C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827812 | |||||||
chr10:50827870 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.769+261T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827870 | |||||||
chr10:50827932 | A | G | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+199T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827932 | |||||||
chr10:50827955 | T | C | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.769+176A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827955 | |||||||
chr10:50827989 | G | A | 3 | a0001c0001t0020g0117a0001c0002t0004g0021a0001c0002t0004g0110 | 4 | HG00621.hp1 NA19011.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+142C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50827989 | |||||||
chr10:50828002 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.769+129T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | 50828002 | |||||||
chr10:50828803 | G | C | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.605-508C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828803 | |||||||
chr10:50828813 | A | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-518T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828813 | |||||||
chr10:50828907 | A | G | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-612T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828907 | |||||||
chr10:50828945 | A | C | 1 | a0001c0001t0005g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.605-650T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50828945 | |||||||
chr10:50829091 | A | G | 7 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-796T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829091 | |||||||
chr10:50829247 | G | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605-952C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829247 | |||||||
chr10:50829268 | T | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605-973A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829268 | |||||||
chr10:50829345 | G | T | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-1050C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829345 | |||||||
chr10:50829399 | G | A | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.605-1104C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829399 | |||||||
chr10:50829666 | C | G | 1 | a0001c0001t0002g0182 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.605-1371G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829666 | |||||||
chr10:50829836 | G | A | 21 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(18): Show | 24 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-1541C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829836 | |||||||
chr10:50829944 | C | G | 1 | a0001c0001t0039g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.605-1649G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50829944 | |||||||
chr10:50830224 | G | T | 1 | a0001c0001t0005g0270 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.605-1929C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830224 | |||||||
chr10:50830370 | G | A | 4 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-2075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830370 | |||||||
chr10:50830485 | A | T | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-2190T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830485 | |||||||
chr10:50830563 | AAAATGAA others(6): Show |
A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-2281_605-2269d others(15): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830563 | |||||||
chr10:50830685 | C | T | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.605-2390G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830685 | |||||||
chr10:50830702 | T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG02083.hp2 NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.605-2407A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830702 | |||||||
chr10:50830806 | G | T | 19 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.605-2511C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830806 | |||||||
chr10:50830876 | A | C | 2 | a0001c0001t0002g0165a0001c0001t0002g0194 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.605-2581T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830876 | |||||||
chr10:50830905 | A | AAAACAGA others(5): Show |
2 | a0001c0002t0004g0021a0001c0002t0004g0110 | 3 | HG00621.hp1 NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.605-2622_605-2611d others(14): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50830905 | |||||||
chr10:50831007 | A | T | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.605-2712T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831007 | |||||||
chr10:50831174 | G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0103 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.605-2879C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831174 | |||||||
chr10:50831262 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.605-2967T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831262 | |||||||
chr10:50831283 | C | T | 2 | a0001c0001t0001g0138a0001c0001t0038g0056 | 2 | HG00673.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.605-2988G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831283 | |||||||
chr10:50831305 | A | G | 12 | a0001c0001t0001g0268a0001c0001t0003g0035a0001c0001t0003g0038others(9): Show | 15 | HG00438.hp1 HG01516.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.605-3010T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831305 | |||||||
chr10:50831451 | G | A | 4 | a0001c0008t0001g0045a0002c0006t0006g0051a0002c0006t0006g0052others(1): Show | 4 | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-3156C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831451 | |||||||
chr10:50831467 | A | G | 19 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.605-3172T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831467 | |||||||
chr10:50831539 | A | T | 1 | a0001c0001t0002g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.605-3244T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831539 | |||||||
chr10:50831588 | C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-3293G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831588 | |||||||
chr10:50831589 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.605-3294C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831589 | |||||||
chr10:50831723 | C | T | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.605-3428G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831723 | |||||||
chr10:50831726 | C | T | 1 | a0001c0001t0032g0059 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.605-3431G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831726 | |||||||
chr10:50831795 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.605-3500G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831795 | |||||||
chr10:50831852 | C | A | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.605-3557G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831852 | |||||||
chr10:50831887 | G | A | 42 | a0001c0001t0001g0268a0001c0001t0003g0019a0001c0001t0003g0035others(39): Show | 53 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.605-3592C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831887 | |||||||
chr10:50831940 | T | C | 18 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(15): Show | 21 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.605-3645A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50831940 | |||||||
chr10:50832047 | G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-3752C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832047 | |||||||
chr10:50832114 | C | T | 1 | a0001c0003t0001g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.605-3819G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832114 | |||||||
chr10:50832185 | T | C | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3889A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832185 | |||||||
chr10:50832227 | G | T | 2 | a0001c0001t0002g0030a0001c0001t0036g0158 | 3 | HG00621.hp2 NA19065.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.604+3847C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832227 | |||||||
chr10:50832253 | G | A | 7 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.604+3821C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832253 | |||||||
chr10:50832390 | A | C | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3684T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832390 | |||||||
chr10:50832494 | C | T | 29 | a0001c0001t0001g0083a0001c0001t0005g0033a0001c0001t0012g0084others(26): Show | 36 | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.604+3580G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832494 | |||||||
chr10:50832505 | A | G | 1 | a0002c0006t0006g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604+3569T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832505 | |||||||
chr10:50832569 | T | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3505A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832569 | |||||||
chr10:50832606 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.604+3468A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832606 | |||||||
chr10:50832700 | A | T | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+3374T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832700 | |||||||
chr10:50832839 | C | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3235G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832839 | |||||||
chr10:50832867 | GT | G | 15 | a0001c0001t0003g0015a0001c0001t0008g0006a0001c0001t0008g0102others(12): Show | 19 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.604+3206delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832867 | |||||||
chr10:50832873 | T | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+3201A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832873 | |||||||
chr10:50832918 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.604+3156A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50832918 | |||||||
chr10:50833143 | A | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2931T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833143 | |||||||
chr10:50833298 | G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2776C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833298 | |||||||
chr10:50833477 | G | C | 1 | a0001c0002t0004g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.604+2597C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833477 | |||||||
chr10:50833661 | G | T | 1 | a0001c0001t0002g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.604+2413C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50833661 | |||||||
chr10:50834010 | T | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(57): Show | 78 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.604+2064A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834010 | |||||||
chr10:50834107 | C | T | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.604+1967G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834107 | |||||||
chr10:50834266 | A | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1808T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834266 | |||||||
chr10:50834479 | G | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1595C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834479 | |||||||
chr10:50834503 | G | C | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604+1571C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834503 | |||||||
chr10:50834592 | G | C | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.604+1482C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834592 | |||||||
chr10:50834629 | A | G | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+1445T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834629 | |||||||
chr10:50834680 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.604+1394G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834680 | |||||||
chr10:50834690 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+1384C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834690 | |||||||
chr10:50834755 | T | C | 4 | a0001c0002t0004g0077a0001c0002t0004g0079a0001c0002t0004g0080others(1): Show | 4 | HG02015.hp1 NA18977.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+1319A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834755 | |||||||
chr10:50834768 | G | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.604+1306C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50834768 | |||||||
chr10:50835087 | A | G | 19 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.604+987T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835087 | |||||||
chr10:50835111 | A | G | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+963T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835111 | |||||||
chr10:50835133 | A | G | 2 | a0001c0001t0009g0161a0001c0001t0009g0162 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.604+941T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835133 | |||||||
chr10:50835355 | G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 71 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.604+719C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835355 | |||||||
chr10:50835494 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.604+580C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835494 | |||||||
chr10:50835805 | CTCTT | C | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+265_604+268del others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835805 | |||||||
chr10:50835884 | T | A | 1 | a0001c0002t0004g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.604+190A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835884 | |||||||
chr10:50835886 | A | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+188T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835886 | |||||||
chr10:50835970 | A | G | 3 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0223 | 3 | HG02132.hp1 NA19079.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.604+104T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835970 | |||||||
chr10:50835988 | CA | C | 19 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.604+85delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | 50835988 | |||||||
chr10:50836380 | G | C | 9 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-68C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836380 | |||||||
chr10:50836539 | T | A | 1 | a0001c0001t0017g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.366-227A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836539 | |||||||
chr10:50836590 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.366-278C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836590 | |||||||
chr10:50836721 | A | G | 1 | a0001c0001t0016g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.366-409T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836721 | |||||||
chr10:50836795 | T | C | 44 | a0001c0001t0001g0224a0001c0001t0001g0268a0001c0001t0003g0019others(41): Show | 55 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.366-483A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50836795 | |||||||
chr10:50837015 | T | C | 1 | a0001c0001t0007g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.366-703A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837015 | |||||||
chr10:50837021 | C | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.366-709G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837021 | |||||||
chr10:50837297 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.366-985G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837297 | |||||||
chr10:50837406 | T | C | 1 | a0001c0001t0005g0274 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.366-1094A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837406 | |||||||
chr10:50837415 | C | T | 4 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(1): Show | 5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1103G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837415 | |||||||
chr10:50837475 | C | A | 9 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.366-1163G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837475 | |||||||
chr10:50837567 | T | A | 3 | a0001c0002t0004g0034a0001c0009t0004g0250a0001c0009t0004g0251 | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1255A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837567 | |||||||
chr10:50837656 | C | T | 1 | a0001c0001t0008g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.366-1344G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837656 | |||||||
chr10:50837831 | T | C | 2 | a0001c0001t0011g0096a0001c0001t0011g0097 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.366-1519A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837831 | |||||||
chr10:50837871 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.366-1559G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837871 | |||||||
chr10:50837894 | A | T | 2 | a0001c0002t0004g0077a0001c0002t0004g0080 | 2 | NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.366-1582T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837894 | |||||||
chr10:50837917 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.366-1605T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50837917 | |||||||
chr10:50838036 | A | G | 7 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.366-1724T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838036 | |||||||
chr10:50838044 | C | T | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1732G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838044 | |||||||
chr10:50838206 | G | A | 4 | a0001c0003t0001g0027a0001c0003t0001g0159a0001c0003t0007g0230others(1): Show | 5 | HG00280.hp2 NA18948.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1894C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838206 | |||||||
chr10:50838272 | G | A | 2 | a0001c0001t0005g0264a0001c0001t0005g0265 | 2 | HG02602.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.366-1960C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838272 | |||||||
chr10:50838344 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.366-2032C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838344 | |||||||
chr10:50838625 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.366-2313G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838625 | |||||||
chr10:50838664 | T | C | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2352A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50838664 | |||||||
chr10:50839156 | C | A | 3 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018 | 6 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+2706G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839156 | |||||||
chr10:50839256 | C | T | 1 | a0001c0008t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.365+2606G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839256 | |||||||
chr10:50839525 | G | A | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.365+2337C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839525 | |||||||
chr10:50839787 | G | A | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+2075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839787 | |||||||
chr10:50839852 | A | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.365+2010T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839852 | |||||||
chr10:50839991 | C | T | 2 | a0001c0001t0010g0036a0001c0001t0010g0101 | 3 | HG01192.hp1 HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.365+1871G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50839991 | |||||||
chr10:50840004 | A | C | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.365+1858T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840004 | |||||||
chr10:50840035 | T | C | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(266): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.365+1827A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840035 | |||||||
chr10:50840196 | A | G | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.365+1666T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840196 | |||||||
chr10:50840217 | G | A | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1645C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840217 | |||||||
chr10:50840240 | A | C | 1 | a0001c0001t0002g0174 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.365+1622T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840240 | |||||||
chr10:50840276 | A | AT | 96 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(93): Show | 113 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.365+1585dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840276 | |||||||
chr10:50840299 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.365+1563G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840299 | |||||||
chr10:50840710 | A | G | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1152T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840710 | |||||||
chr10:50840848 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.365+1014C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50840848 | |||||||
chr10:50841028 | A | G | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.365+834T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841028 | |||||||
chr10:50841173 | A | G | 1 | a0001c0001t0003g0277 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.365+689T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841173 | |||||||
chr10:50841318 | C | T | 6 | a0001c0001t0038g0056a0001c0008t0001g0045a0001c0008t0017g0049others(3): Show | 6 | HG02451.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+544G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841318 | |||||||
chr10:50841477 | G | A | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.365+385C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | 50841477 | |||||||
chr10:50842074 | A | AAC | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-84_235-83dupGT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842074 | |||||||
chr10:50842140 | A | G | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.235-148T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842140 | |||||||
chr10:50842153 | T | G | 1 | a0001c0003t0001g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.235-161A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842153 | |||||||
chr10:50842303 | T | C | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235-311A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842303 | |||||||
chr10:50842472 | G | A | 1 | a0001c0002t0004g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235-480C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842472 | |||||||
chr10:50842476 | T | C | 1 | a0001c0001t0040g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-484A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842476 | |||||||
chr10:50842700 | C | G | 1 | a0001c0001t0015g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.235-708G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50842700 | |||||||
chr10:50843053 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.234+935C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843053 | |||||||
chr10:50843367 | T | A | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+621A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843367 | |||||||
chr10:50843482 | T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.234+506A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843482 | |||||||
chr10:50843899 | C | T | 31 | a0001c0001t0003g0019a0001c0001t0003g0255a0001c0001t0003g0261others(28): Show | 39 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.234+89G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 4/12 | chr10 | 50843899 | |||||||
chr10:50844185 | C | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-63G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844185 | |||||||
chr10:50844362 | AAT | A | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-242_100-241del others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844362 | |||||||
chr10:50844563 | A | C | 273 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(270): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.100-441T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844563 | |||||||
chr10:50844708 | A | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-586T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844708 | |||||||
chr10:50844719 | C | T | 18 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(15): Show | 25 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-597G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844719 | |||||||
chr10:50844749 | G | A | 1 | a0001c0002t0004g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100-627C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844749 | |||||||
chr10:50844839 | T | C | 1 | a0001c0001t0005g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-717A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50844839 | |||||||
chr10:50845326 | C | A | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-1204G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845326 | |||||||
chr10:50845559 | AT | A | 11 | a0001c0002t0004g0002a0001c0002t0004g0020a0001c0002t0004g0075others(8): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-1438delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845559 | |||||||
chr10:50845911 | G | A | 3 | a0001c0001t0002g0057a0001c0001t0002g0154a0001c0001t0002g0164 | 3 | HG00673.hp1 NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.100-1789C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845911 | |||||||
chr10:50845953 | C | CA | 83 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.100-1832dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845953 | |||||||
chr10:50845953 | CA | C | 8 | a0001c0001t0002g0174a0001c0001t0008g0006a0001c0001t0008g0102others(5): Show | 10 | HG02135.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-1832delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50845953 | |||||||
chr10:50846046 | C | T | 1 | a0001c0001t0023g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.100-1924G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846046 | |||||||
chr10:50846097 | C | A | 15 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(12): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-1975G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846097 | |||||||
chr10:50846137 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.100-2015T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846137 | |||||||
chr10:50846214 | C | A | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-2092G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846214 | |||||||
chr10:50846384 | A | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2262T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846384 | |||||||
chr10:50846495 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-2373G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846495 | |||||||
chr10:50846606 | A | G | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2484T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846606 | |||||||
chr10:50846728 | A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(80): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.100-2606T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846728 | |||||||
chr10:50846821 | T | A | 1 | a0001c0001t0043g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-2699A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846821 | |||||||
chr10:50846916 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-2794C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50846916 | |||||||
chr10:50847261 | G | A | 1 | a0002c0004t0044g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-3139C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847261 | |||||||
chr10:50847479 | A | T | 1 | a0001c0001t0015g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-3357T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847479 | |||||||
chr10:50847743 | C | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-3621G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847743 | |||||||
chr10:50847872 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-3750C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847872 | |||||||
chr10:50847965 | C | A | 3 | a0001c0002t0004g0034a0001c0009t0004g0250a0001c0009t0004g0251 | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3843G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50847965 | |||||||
chr10:50848012 | C | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-3890G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848012 | |||||||
chr10:50848145 | A | T | 2 | a0001c0002t0004g0090a0001c0002t0013g0089 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.100-4023T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848145 | |||||||
chr10:50848354 | C | G | 1 | a0001c0001t0003g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-4232G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848354 | |||||||
chr10:50848520 | A | C | 1 | a0001c0002t0004g0079 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100-4398T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848520 | |||||||
chr10:50848642 | A | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-4520T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848642 | |||||||
chr10:50848851 | G | A | 2 | a0001c0001t0001g0191a0001c0001t0002g0168 | 2 | HG02273.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.100-4729C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848851 | |||||||
chr10:50848897 | A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(118): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.100-4775T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50848897 | |||||||
chr10:50849010 | G | T | 2 | a0001c0001t0011g0096a0001c0001t0011g0097 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.100-4888C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849010 | |||||||
chr10:50849085 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-4963A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849085 | |||||||
chr10:50849142 | A | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-5020T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849142 | |||||||
chr10:50849195 | A | G | 3 | a0001c0005t0001g0205a0001c0005t0024g0206a0001c0005t0048g0207 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-5073T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849195 | |||||||
chr10:50849208 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-5086C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849208 | |||||||
chr10:50849248 | T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0172others(75): Show | 103 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.100-5126A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849248 | |||||||
chr10:50849253 | A | G | 1 | a0001c0001t0002g0007 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.100-5131T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849253 | |||||||
chr10:50849370 | C | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-5248G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849370 | |||||||
chr10:50849438 | G | A | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-5316C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849438 | |||||||
chr10:50849559 | A | G | 11 | a0001c0002t0004g0002a0001c0002t0004g0020a0001c0002t0004g0075others(8): Show | 16 | HG00423.hp2 HG00597.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-5437T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849559 | |||||||
chr10:50849740 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.100-5618C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849740 | |||||||
chr10:50849786 | C | CT | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(166): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.100-5665dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849786 | |||||||
chr10:50849786 | C | CTT | 21 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0132others(18): Show | 21 | HG00544.hp2 HG01123.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-5666_100-5665d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849786 | |||||||
chr10:50849889 | C | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-5767G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849889 | |||||||
chr10:50849938 | C | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-5816G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849938 | |||||||
chr10:50849962 | T | G | 1 | a0001c0001t0002g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100-5840A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50849962 | |||||||
chr10:50850004 | C | T | 1 | a0001c0003t0001g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.100-5882G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850004 | |||||||
chr10:50850154 | G | A | 19 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(16): Show | 26 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-6032C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850154 | |||||||
chr10:50850217 | T | C | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0049g0170 | 3 | HG00438.hp2 HG00558.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.100-6095A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850217 | |||||||
chr10:50850578 | A | G | 1 | a0001c0001t0005g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100-6456T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850578 | |||||||
chr10:50850592 | T | TTG | 58 | a0001c0001t0001g0268a0001c0001t0003g0019a0001c0001t0003g0035others(55): Show | 72 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.100-6472_100-6471d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850592 | |||||||
chr10:50850978 | G | T | 5 | a0001c0008t0001g0045a0001c0008t0017g0049a0002c0006t0006g0051others(2): Show | 5 | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6856C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50850978 | |||||||
chr10:50851005 | C | G | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-6883G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851005 | |||||||
chr10:50851327 | A | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-7205T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851327 | |||||||
chr10:50851610 | GTC | G | 12 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(9): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-7490_100-7489d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851610 | |||||||
chr10:50851658 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-7536C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851658 | |||||||
chr10:50851956 | T | C | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-7834A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50851956 | |||||||
chr10:50852185 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+7657G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852185 | |||||||
chr10:50852341 | G | A | 42 | a0001c0001t0001g0268a0001c0001t0003g0019a0001c0001t0003g0035others(39): Show | 53 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+7501C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852341 | |||||||
chr10:50852453 | T | C | 1 | a0001c0008t0017g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+7389A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852453 | |||||||
chr10:50852576 | C | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0197 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.99+7266G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852576 | |||||||
chr10:50852761 | A | G | 1 | a0001c0001t0003g0166 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.99+7081T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852761 | |||||||
chr10:50852869 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+6973G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852869 | |||||||
chr10:50852882 | C | T | 1 | a0001c0002t0004g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+6960G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852882 | |||||||
chr10:50852902 | C | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0172others(73): Show | 101 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+6940G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852902 | |||||||
chr10:50852950 | C | T | 2 | a0001c0001t0029g0058a0002c0004t0045g0199 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.99+6892G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50852950 | |||||||
chr10:50853040 | G | A | 1 | a0001c0001t0040g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+6802C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853040 | |||||||
chr10:50853042 | G | A | 5 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+6800C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853042 | |||||||
chr10:50853091 | G | C | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+6751C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853091 | |||||||
chr10:50853133 | G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6709C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853133 | |||||||
chr10:50853187 | T | C | 1 | a0001c0001t0003g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+6655A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853187 | |||||||
chr10:50853275 | C | T | 273 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(270): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.99+6567G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853275 | |||||||
chr10:50853382 | A | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+6460T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853382 | |||||||
chr10:50853465 | G | A | 1 | a0001c0012t0035g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+6377C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853465 | |||||||
chr10:50853750 | AT | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0022others(154): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.99+6091delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853750 | |||||||
chr10:50853750 | ATT | A | 18 | a0001c0001t0003g0065a0001c0001t0003g0066a0001c0001t0003g0067others(15): Show | 19 | HG00423.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+6090_99+6091del others(2): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853750 | |||||||
chr10:50853773 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+6069C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853773 | |||||||
chr10:50853797 | T | A | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+6045A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853797 | |||||||
chr10:50853801 | T | C | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+6041A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853801 | |||||||
chr10:50853803 | T | TA | 11 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+6038dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853803 | |||||||
chr10:50853804 | A | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(241): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.99+6038T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853804 | |||||||
chr10:50853805 | A | T | 1 | a0001c0001t0023g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.99+6037T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853805 | |||||||
chr10:50853823 | TA | T | 43 | a0001c0001t0001g0268a0001c0001t0003g0019a0001c0001t0003g0035others(40): Show | 54 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.99+6018delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853823 | |||||||
chr10:50853891 | A | T | 1 | a0001c0002t0004g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+5951T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50853891 | |||||||
chr10:50854115 | T | C | 2 | a0001c0001t0005g0033a0001c0001t0014g0249 | 3 | HG01109.hp2 HG01167.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.99+5727A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854115 | |||||||
chr10:50854200 | A | C | 2 | a0001c0001t0002g0165a0001c0001t0002g0194 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.99+5642T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854200 | |||||||
chr10:50854429 | A | G | 7 | a0001c0001t0005g0269a0001c0001t0005g0270a0001c0001t0005g0272others(4): Show | 7 | HG02280.hp1 HG03654.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+5413T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854429 | |||||||
chr10:50854998 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+4844G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50854998 | |||||||
chr10:50855053 | T | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+4789A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855053 | |||||||
chr10:50855095 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.99+4747A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855095 | |||||||
chr10:50855245 | G | C | 2 | a0002c0004t0018g0040a0002c0004t0018g0156 | 2 | HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.99+4597C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855245 | |||||||
chr10:50855262 | T | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(52): Show | 73 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+4580A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855262 | |||||||
chr10:50855288 | A | C | 1 | a0002c0006t0006g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+4554T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855288 | |||||||
chr10:50855360 | A | T | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.99+4482T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855360 | |||||||
chr10:50855361 | T | G | 1 | a0002c0006t0006g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+4481A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855361 | |||||||
chr10:50855385 | T | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+4457A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855385 | |||||||
chr10:50855510 | C | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0172others(74): Show | 102 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+4332G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855510 | |||||||
chr10:50855671 | C | A | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.99+4171G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855671 | |||||||
chr10:50855911 | C | G | 15 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(12): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+3931G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50855911 | |||||||
chr10:50856273 | G | A | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.99+3569C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856273 | |||||||
chr10:50856287 | A | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0172others(75): Show | 103 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.99+3555T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856287 | |||||||
chr10:50856307 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+3535G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856307 | |||||||
chr10:50856463 | C | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(109): Show | 133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.99+3379G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856463 | |||||||
chr10:50856509 | G | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(106): Show | 130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.99+3333C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856509 | |||||||
chr10:50856558 | T | C | 1 | a0001c0002t0004g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+3284A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856558 | |||||||
chr10:50856582 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.99+3260T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856582 | |||||||
chr10:50856722 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+3120C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856722 | |||||||
chr10:50856800 | TGTG | T | 1 | a0001c0001t0005g0011 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+3039_99+3041del others(3): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856800 | |||||||
chr10:50856823 | G | A | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+3019C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856823 | |||||||
chr10:50856951 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.99+2891G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856951 | |||||||
chr10:50856976 | C | T | 1 | a0001c0008t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.99+2866G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50856976 | |||||||
chr10:50857083 | T | C | 1 | a0001c0001t0005g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.99+2759A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857083 | |||||||
chr10:50857162 | C | T | 8 | a0001c0001t0001g0022a0001c0001t0005g0269a0001c0001t0005g0270others(5): Show | 9 | HG02280.hp1 HG03654.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2680G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857162 | |||||||
chr10:50857187 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+2655G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857187 | |||||||
chr10:50857237 | G | A | 2 | a0001c0002t0004g0091a0001c0012t0035g0157 | 2 | HG03225.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.99+2605C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857237 | |||||||
chr10:50857646 | C | G | 1 | a0001c0001t0003g0017 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.99+2196G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857646 | |||||||
chr10:50857778 | T | C | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+2064A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857778 | |||||||
chr10:50857815 | G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+2027C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857815 | |||||||
chr10:50857975 | A | T | 1 | a0001c0001t0005g0011 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99+1867T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857975 | |||||||
chr10:50857985 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.99+1857G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50857985 | |||||||
chr10:50858310 | TG | T | 22 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(19): Show | 25 | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.99+1531delC | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858310 | |||||||
chr10:50858603 | G | C | 1 | a0001c0001t0012g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+1239C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858603 | |||||||
chr10:50858615 | T | C | 1 | a0001c0002t0004g0252 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+1227A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858615 | |||||||
chr10:50858935 | G | A | 2 | a0001c0002t0004g0021a0001c0002t0004g0110 | 3 | HG00621.hp1 NA19011.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.99+907C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50858935 | |||||||
chr10:50859031 | G | T | 1 | a0001c0001t0005g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.99+811C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859031 | |||||||
chr10:50859037 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+805G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859037 | |||||||
chr10:50859049 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+793A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859049 | |||||||
chr10:50859268 | A | G | 2 | a0001c0001t0029g0058a0002c0004t0045g0199 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.99+574T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859268 | |||||||
chr10:50859414 | C | T | 1 | a0001c0001t0005g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+428G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859414 | |||||||
chr10:50859464 | G | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.99+378C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859464 | |||||||
chr10:50859527 | C | T | 1 | a0001c0005t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+315G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859527 | |||||||
chr10:50859675 | T | C | 1 | a0001c0001t0005g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+167A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859675 | |||||||
chr10:50859814 | A | G | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+28T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | 50859814 | |||||||
chr10:50860152 | A | G | 1 | a0001c0001t0021g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-45-167T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860152 | |||||||
chr10:50860192 | C | CA | 15 | a0001c0001t0003g0035a0001c0001t0003g0253a0001c0001t0009g0028others(12): Show | 17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-45-208dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860192 | |||||||
chr10:50860196 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-45-211T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860196 | |||||||
chr10:50860449 | G | C | 1 | a0001c0001t0002g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-45-464C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860449 | |||||||
chr10:50860683 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-45-698C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860683 | |||||||
chr10:50860705 | G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(254): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.-45-720C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860705 | |||||||
chr10:50860930 | T | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-45-945A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50860930 | |||||||
chr10:50861038 | T | C | 3 | a0001c0005t0001g0205a0001c0005t0024g0206a0001c0005t0048g0207 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-45-1053A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861038 | |||||||
chr10:50861051 | G | C | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-45-1066C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861051 | |||||||
chr10:50861060 | G | A | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-45-1075C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861060 | |||||||
chr10:50861440 | A | G | 1 | a0001c0002t0004g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-45-1455T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861440 | |||||||
chr10:50861502 | G | C | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-45-1517C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861502 | |||||||
chr10:50861513 | T | C | 1 | a0001c0001t0019g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45-1528A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861513 | |||||||
chr10:50861771 | A | G | 1 | a0001c0001t0023g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-45-1786T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861771 | |||||||
chr10:50861784 | A | G | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-45-1799T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861784 | |||||||
chr10:50861804 | T | C | 2 | a0001c0001t0016g0048a0001c0001t0040g0044 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-1819A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861804 | |||||||
chr10:50861856 | A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(263): Show | 327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-45-1871T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861856 | |||||||
chr10:50861947 | C | T | 1 | a0001c0001t0005g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-45-1962G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861947 | |||||||
chr10:50861992 | G | C | 30 | a0001c0001t0003g0019a0001c0001t0003g0255a0001c0001t0003g0261others(27): Show | 38 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.-45-2007C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50861992 | |||||||
chr10:50862163 | C | T | 1 | a0003c0010t0001g0139 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-46+1870G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50862163 | |||||||
chr10:50862974 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-46+1059G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50862974 | |||||||
chr10:50863043 | G | T | 2 | a0001c0001t0005g0269a0001c0001t0049g0170 | 2 | NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-46+990C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863043 | |||||||
chr10:50863116 | T | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+917A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863116 | |||||||
chr10:50863128 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-46+905G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863128 | |||||||
chr10:50863269 | C | T | 4 | a0001c0001t0021g0115a0001c0005t0001g0205a0001c0005t0024g0206others(1): Show | 4 | HG01257.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+764G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863269 | |||||||
chr10:50863319 | G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0103 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-46+714C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863319 | |||||||
chr10:50863417 | A | G | 1 | a0001c0001t0001g0022 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-46+616T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863417 | |||||||
chr10:50863484 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-46+549T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863484 | |||||||
chr10:50863567 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-46+466C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863567 | |||||||
chr10:50863633 | G | T | 1 | a0001c0003t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-46+400C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863633 | |||||||
chr10:50863653 | A | T | 1 | a0002c0004t0018g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-46+380T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863653 | |||||||
chr10:50863673 | A | G | 14 | a0001c0001t0009g0028a0001c0001t0009g0161a0001c0001t0009g0162others(11): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-46+360T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863673 | |||||||
chr10:50863733 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+300C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863733 | |||||||
chr10:50863774 | A | G | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+259T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863774 | |||||||
chr10:50863825 | T | A | 20 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46+208A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863825 | |||||||
chr10:50863826 | A | C | 20 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46+207T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863826 | |||||||
chr10:50863902 | G | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-46+131C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | 50863902 | |||||||
chr10:50864082 | T | C | 1 | a0002c0006t0006g0053 | 1 | HG02451.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-93-2A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864082 | |||||||
chr10:50864159 | C | T | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-79G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864159 | |||||||
chr10:50864199 | A | C | 4 | a0001c0001t0001g0118a0001c0001t0020g0117a0001c0002t0004g0021others(1): Show | 5 | HG00621.hp1 NA19002.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-119T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864199 | |||||||
chr10:50864429 | T | C | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-349A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864429 | |||||||
chr10:50864441 | G | C | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-361C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864441 | |||||||
chr10:50864535 | A | G | 1 | a0001c0001t0005g0256 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-93-455T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864535 | |||||||
chr10:50864542 | G | GT | 91 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-93-463dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864542 | |||||||
chr10:50864618 | T | C | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-538A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864618 | |||||||
chr10:50864620 | T | C | 1 | a0001c0001t0043g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-93-540A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864620 | |||||||
chr10:50864679 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-599G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864679 | |||||||
chr10:50864690 | C | T | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-610G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864690 | |||||||
chr10:50864721 | C | T | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-641G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864721 | |||||||
chr10:50864744 | G | A | 1 | a0001c0001t0003g0016 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-93-664C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864744 | |||||||
chr10:50864826 | C | T | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-746G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864826 | |||||||
chr10:50864907 | C | T | 2 | a0001c0001t0005g0272a0001c0001t0005g0273 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-93-827G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864907 | |||||||
chr10:50864908 | G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-93-828C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864908 | |||||||
chr10:50864919 | A | G | 1 | a0001c0001t0003g0019 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-93-839T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50864919 | |||||||
chr10:50865223 | C | A | 2 | a0001c0001t0005g0033a0001c0001t0014g0249 | 3 | HG01109.hp2 HG01167.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-93-1143G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865223 | |||||||
chr10:50865232 | C | CTGGG | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-1156_-93-1153d others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865232 | |||||||
chr10:50865250 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-93-1170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865250 | |||||||
chr10:50865296 | T | TTAC | 20 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93-1219_-93-1217d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865296 | |||||||
chr10:50865296 | TTAC | T | 19 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93-1219_-93-1217d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865296 | |||||||
chr10:50865302 | C | G | 2 | a0001c0001t0029g0058a0002c0004t0045g0199 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-93-1222G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865302 | |||||||
chr10:50865388 | G | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93-1308C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865388 | |||||||
chr10:50865421 | A | T | 1 | a0001c0001t0010g0036 | 2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-93-1341T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865421 | |||||||
chr10:50865510 | A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(53): Show | 74 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-93-1430T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865510 | |||||||
chr10:50865603 | T | C | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-1523A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865603 | |||||||
chr10:50865733 | G | T | 2 | a0001c0001t0001g0116a0001c0001t0003g0017 | 3 | HG00280.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-93-1653C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865733 | |||||||
chr10:50865853 | C | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-1773G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50865853 | |||||||
chr10:50866011 | A | G | 1 | a0001c0001t0041g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-93-1931T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866011 | |||||||
chr10:50866013 | A | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-1933T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866013 | |||||||
chr10:50866042 | G | C | 1 | a0001c0002t0004g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-93-1962C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866042 | |||||||
chr10:50866079 | T | C | 20 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(17): Show | 23 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93-1999A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866079 | |||||||
chr10:50866087 | C | T | 28 | a0001c0001t0001g0083a0001c0001t0005g0033a0001c0001t0012g0084others(25): Show | 35 | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-93-2007G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866087 | |||||||
chr10:50866760 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-2680C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866760 | |||||||
chr10:50866760 | G | T | 1 | a0001c0001t0003g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-93-2680C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866760 | |||||||
chr10:50866908 | G | A | 1 | a0001c0008t0017g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-93-2828C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50866908 | |||||||
chr10:50867016 | GT | G | 16 | a0001c0001t0003g0276a0001c0001t0008g0006a0001c0001t0008g0102others(13): Show | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-93-2937delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867016 | |||||||
chr10:50867151 | C | T | 1 | a0001c0002t0013g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-93-3071G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867151 | |||||||
chr10:50867204 | A | C | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-93-3124T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867204 | |||||||
chr10:50867270 | T | C | 1 | a0001c0002t0004g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-93-3190A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867270 | |||||||
chr10:50867321 | G | A | 3 | a0001c0005t0001g0205a0001c0005t0024g0206a0001c0005t0048g0207 | 3 | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-93-3241C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867321 | |||||||
chr10:50867464 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-93-3384A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867464 | |||||||
chr10:50867685 | A | G | 1 | a0001c0001t0010g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-93-3605T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867685 | |||||||
chr10:50867765 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-93-3685T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867765 | |||||||
chr10:50867786 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-93-3706C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867786 | |||||||
chr10:50867812 | G | T | 20 | a0001c0001t0001g0012a0001c0001t0002g0062a0001c0001t0003g0013others(17): Show | 27 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-93-3732C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867812 | |||||||
chr10:50867841 | A | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-3761T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867841 | |||||||
chr10:50867901 | C | T | 2 | a0001c0001t0008g0006a0001c0001t0008g0102 | 4 | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93-3821G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50867901 | |||||||
chr10:50868038 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-3958C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868038 | |||||||
chr10:50868144 | T | A | 2 | a0001c0001t0001g0136a0001c0001t0028g0088 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-93-4064A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868144 | |||||||
chr10:50868186 | T | G | 1 | a0001c0001t0002g0195 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-93-4106A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868186 | |||||||
chr10:50868192 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-93-4112G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868192 | |||||||
chr10:50868222 | A | G | 1 | a0001c0001t0043g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-93-4142T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868222 | |||||||
chr10:50868506 | A | C | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-93-4426T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868506 | |||||||
chr10:50868801 | A | T | 19 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(16): Show | 22 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93-4721T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868801 | |||||||
chr10:50868973 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-93-4893A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50868973 | |||||||
chr10:50869312 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-5232C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869312 | |||||||
chr10:50869441 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-93-5361C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869441 | |||||||
chr10:50869812 | C | A | 58 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(55): Show | 76 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-93-5732G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50869812 | |||||||
chr10:50870098 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-93-6018G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870098 | |||||||
chr10:50870379 | G | A | 3 | a0001c0002t0004g0034a0001c0009t0004g0250a0001c0009t0004g0251 | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-6299C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870379 | |||||||
chr10:50870425 | G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(97): Show | 129 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-93-6345C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870425 | |||||||
chr10:50870499 | A | C | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-6419T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870499 | |||||||
chr10:50870665 | G | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0191others(98): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-93-6585C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870665 | |||||||
chr10:50870822 | C | A | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-93-6742G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870822 | |||||||
chr10:50870902 | G | C | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 21 | HG00673.hp2 HG02135.hp1 HG02148.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93-6822C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870902 | |||||||
chr10:50870968 | T | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(266): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-93-6888A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50870968 | |||||||
chr10:50871130 | A | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-7050T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871130 | |||||||
chr10:50871325 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-93-7245G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871325 | |||||||
chr10:50871326 | G | A | 3 | a0001c0001t0029g0058a0001c0002t0013g0092a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-93-7246C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871326 | |||||||
chr10:50871503 | T | C | 1 | a0001c0001t0005g0011 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-93-7423A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871503 | |||||||
chr10:50871569 | G | C | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-93-7489C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871569 | |||||||
chr10:50871805 | T | C | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0038g0056 | 5 | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-7725A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871805 | |||||||
chr10:50871816 | C | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-93-7736G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871816 | |||||||
chr10:50871981 | A | T | 273 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(270): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-93-7901T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50871981 | |||||||
chr10:50872020 | ATAT | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0103 | 3 | NA18947.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-93-7943_-93-7941d others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872020 | |||||||
chr10:50872023 | T | C | 12 | a0001c0001t0001g0031a0001c0001t0001g0200a0001c0001t0001g0201others(9): Show | 13 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93-7943A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872023 | |||||||
chr10:50872128 | C | CTT | 17 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(14): Show | 20 | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.-93-8049_-93-8048i others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872128 | |||||||
chr10:50872220 | A | G | 1 | a0001c0002t0004g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-93-8140T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872220 | |||||||
chr10:50872353 | A | G | 1 | a0001c0001t0005g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-93-8273T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872353 | |||||||
chr10:50872525 | G | A | 1 | a0001c0001t0003g0277 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-93-8445C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872525 | |||||||
chr10:50872668 | G | A | 3 | a0001c0001t0029g0058a0002c0004t0044g0055a0002c0004t0045g0199 | 3 | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-8588C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872668 | |||||||
chr10:50872779 | C | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-8699G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872779 | |||||||
chr10:50872828 | T | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-8748A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872828 | |||||||
chr10:50872898 | A | C | 1 | a0001c0001t0021g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-93-8818T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872898 | |||||||
chr10:50872905 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-93-8825C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872905 | |||||||
chr10:50872946 | C | CT | 56 | a0001c0001t0001g0012a0001c0001t0001g0095a0001c0001t0001g0108others(53): Show | 66 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-93-8867dupA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872946 | C | CTT | 8 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0002g0164others(5): Show | 9 | HG00140.hp1 HG00558.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93-8868_-93-8867d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872946 | CT | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0103others(83): Show | 110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-93-8867delA | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872946 | CTT | C | 9 | a0001c0001t0001g0197a0001c0001t0002g0009a0001c0001t0002g0030others(6): Show | 12 | HG00621.hp2 HG00639.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93-8868_-93-8867d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872946 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(4): Show | 10 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93-8877_-93-8867d others(13): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872946 | CTTTTTTT others(7): Show |
C | 12 | a0001c0001t0001g0268a0001c0001t0003g0035a0001c0001t0003g0038others(9): Show | 15 | HG00438.hp1 HG01516.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-93-8880_-93-8867d others(16): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872946 | |||||||
chr10:50872986 | C | T | 1 | a0001c0003t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-93-8906G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872986 | |||||||
chr10:50872987 | G | A | 2 | a0001c0001t0038g0056a0002c0004t0044g0055 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-93-8907C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872987 | |||||||
chr10:50872997 | C | G | 2 | a0001c0001t0029g0058a0002c0004t0045g0199 | 2 | HG01069.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-93-8917G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50872997 | |||||||
chr10:50873231 | T | C | 8 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0009g0028others(5): Show | 11 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93-9151A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873231 | |||||||
chr10:50873248 | G | T | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(230): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-93-9168C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873248 | |||||||
chr10:50873290 | A | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-93-9210T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873290 | |||||||
chr10:50873538 | A | G | 1 | a0001c0001t0003g0019 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-93-9458T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873538 | |||||||
chr10:50873575 | A | G | 17 | a0001c0001t0001g0031a0001c0001t0001g0200a0001c0001t0001g0201others(14): Show | 18 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-93-9495T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873575 | |||||||
chr10:50873585 | A | T | 1 | a0002c0004t0045g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93-9505T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873585 | |||||||
chr10:50873699 | C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0069others(94): Show | 123 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-93-9619G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873699 | |||||||
chr10:50873801 | G | C | 3 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018 | 6 | HG01257.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93-9721C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873801 | |||||||
chr10:50873960 | T | C | 1 | a0001c0003t0001g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-93-9880A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50873960 | |||||||
chr10:50874158 | G | A | 2 | a0001c0002t0004g0090a0001c0002t0013g0089 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-93-10078C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874158 | |||||||
chr10:50874204 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-93-10124C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874204 | |||||||
chr10:50874223 | T | C | 1 | a0002c0004t0006g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-93-10143A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874223 | |||||||
chr10:50874265 | A | G | 1 | a0001c0001t0002g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-93-10185T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874265 | |||||||
chr10:50874290 | TA | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(37): Show | 48 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-93-10211delT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874290 | |||||||
chr10:50874845 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-94+10736G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874845 | |||||||
chr10:50874893 | T | C | 2 | a0001c0001t0038g0056a0002c0004t0044g0055 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+10688A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874893 | |||||||
chr10:50874948 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+10633C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50874948 | |||||||
chr10:50875061 | G | A | 36 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(33): Show | 43 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-94+10520C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875061 | |||||||
chr10:50875141 | T | C | 1 | a0001c0003t0001g0226 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-94+10440A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875141 | |||||||
chr10:50875285 | T | TA | 36 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(33): Show | 43 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-94+10295dupT | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875285 | |||||||
chr10:50875343 | A | T | 4 | a0001c0003t0001g0027a0001c0003t0001g0159a0001c0003t0007g0230others(1): Show | 5 | HG00280.hp2 NA18948.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94+10238T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875343 | |||||||
chr10:50875411 | C | T | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+10170G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875411 | |||||||
chr10:50875419 | G | A | 3 | a0001c0012t0035g0157a0002c0004t0018g0040a0002c0004t0018g0156 | 3 | HG02886.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-94+10162C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875419 | |||||||
chr10:50875480 | A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(20): Show | 30 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-94+10101T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875480 | |||||||
chr10:50875667 | T | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+9914A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875667 | |||||||
chr10:50875961 | T | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+9620A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50875961 | |||||||
chr10:50876194 | G | A | 11 | a0001c0001t0005g0050a0001c0001t0011g0096a0001c0001t0011g0097others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-94+9387C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876194 | |||||||
chr10:50876593 | T | C | 1 | a0001c0003t0001g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-94+8988A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876593 | |||||||
chr10:50876598 | G | A | 1 | a0001c0001t0031g0228 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-94+8983C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876598 | |||||||
chr10:50876648 | C | T | 1 | a0001c0001t0036g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-94+8933G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876648 | |||||||
chr10:50876658 | C | A | 1 | a0001c0001t0015g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-94+8923G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876658 | |||||||
chr10:50876742 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-94+8839G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876742 | |||||||
chr10:50876769 | T | C | 7 | a0001c0001t0003g0035a0001c0001t0003g0038a0001c0001t0003g0039others(4): Show | 10 | HG02523.hp1 HG02602.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-94+8812A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876769 | |||||||
chr10:50876846 | TAC | T | 3 | a0001c0012t0035g0157a0002c0004t0018g0040a0002c0004t0018g0156 | 3 | HG02886.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-94+8733_-94+8734d others(4): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876846 | |||||||
chr10:50876904 | C | T | 6 | a0001c0001t0005g0050a0001c0008t0001g0045a0001c0008t0017g0049others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+8677G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50876904 | |||||||
chr10:50877267 | C | T | 1 | a0001c0001t0003g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-94+8314G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877267 | |||||||
chr10:50877334 | A | G | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-94+8247T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877334 | |||||||
chr10:50877531 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-94+8050T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877531 | |||||||
chr10:50877536 | C | T | 2 | a0001c0001t0011g0096a0001c0001t0011g0097 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-94+8045G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877536 | |||||||
chr10:50877615 | T | C | 1 | a0001c0003t0001g0229 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-94+7966A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877615 | |||||||
chr10:50877796 | T | C | 5 | a0001c0001t0005g0050a0001c0008t0001g0045a0002c0006t0006g0051others(2): Show | 5 | HG01884.hp1 HG02451.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-94+7785A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877796 | |||||||
chr10:50877848 | C | T | 13 | a0001c0001t0005g0050a0001c0001t0011g0096a0001c0001t0011g0097others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+7733G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877848 | |||||||
chr10:50877849 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+7732C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877849 | |||||||
chr10:50877989 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-94+7592C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50877989 | |||||||
chr10:50878017 | G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0244 | 3 | NA19066.hp1 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-94+7564C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878017 | |||||||
chr10:50878063 | A | G | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG00738.hp2 HG01081.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+7518T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878063 | |||||||
chr10:50878098 | G | A | 2 | a0001c0007t0005g0242a0001c0007t0034g0243 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-94+7483C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878098 | |||||||
chr10:50878165 | A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(42): Show | 58 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+7416T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878165 | |||||||
chr10:50878350 | G | T | 13 | a0001c0001t0005g0050a0001c0001t0011g0096a0001c0001t0011g0097others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+7231C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878350 | |||||||
chr10:50878567 | G | C | 1 | a0001c0001t0038g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-94+7014C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878567 | |||||||
chr10:50878603 | T | G | 2 | a0001c0003t0007g0230a0001c0003t0007g0231 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-94+6978A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878603 | |||||||
chr10:50878667 | C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0154 | 2 | NA18947.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-94+6914G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878667 | |||||||
chr10:50878695 | T | A | 13 | a0001c0001t0005g0050a0001c0001t0011g0096a0001c0001t0011g0097others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+6886A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878695 | |||||||
chr10:50878709 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-94+6872G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878709 | |||||||
chr10:50878918 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-94+6663G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50878918 | |||||||
chr10:50879098 | G | A | 2 | a0001c0001t0038g0056a0002c0004t0044g0055 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+6483C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879098 | |||||||
chr10:50879173 | T | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(225): Show | 280 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.-94+6408A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879173 | |||||||
chr10:50879236 | T | C | 2 | a0001c0002t0004g0091a0001c0002t0013g0092 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-94+6345A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879236 | |||||||
chr10:50879400 | G | T | 1 | a0001c0002t0004g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-94+6181C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879400 | |||||||
chr10:50879586 | C | T | 1 | a0001c0001t0005g0256 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-94+5995G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879586 | |||||||
chr10:50879897 | G | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(44): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+5684C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50879897 | |||||||
chr10:50880499 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-94+5082G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880499 | |||||||
chr10:50880521 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-94+5060C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880521 | |||||||
chr10:50880633 | G | T | 5 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0010g0101others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+4948C>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880633 | |||||||
chr10:50880857 | G | A | 1 | a0001c0001t0005g0011 | 3 | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-94+4724C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50880857 | |||||||
chr10:50881029 | G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 11 | HG00738.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-94+4552C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881029 | |||||||
chr10:50881077 | C | A | 1 | a0001c0001t0002g0236 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-94+4504G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881077 | |||||||
chr10:50881084 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-94+4497C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881084 | |||||||
chr10:50881101 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-94+4480G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881101 | |||||||
chr10:50881102 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-94+4479C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881102 | |||||||
chr10:50881134 | T | C | 1 | a0001c0001t0005g0238 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-94+4447A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881134 | |||||||
chr10:50881257 | C | A | 5 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0010g0101others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+4324G>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881257 | |||||||
chr10:50881437 | G | C | 2 | a0001c0001t0019g0239a0001c0001t0019g0240 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-94+4144C>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881437 | |||||||
chr10:50881439 | C | T | 26 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(23): Show | 33 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-94+4142G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881439 | |||||||
chr10:50881495 | G | A | 1 | a0001c0001t0005g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-94+4086C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881495 | |||||||
chr10:50881783 | G | A | 5 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0010g0101others(2): Show | 7 | HG01192.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+3798C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881783 | |||||||
chr10:50881804 | T | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-94+3777A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881804 | |||||||
chr10:50881819 | T | C | 2 | a0001c0001t0038g0056a0002c0004t0044g0055 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-94+3762A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881819 | |||||||
chr10:50881913 | T | G | 1 | a0001c0002t0004g0252 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-94+3668A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50881913 | |||||||
chr10:50882028 | T | G | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(256): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-94+3553A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882028 | |||||||
chr10:50882282 | A | G | 1 | a0001c0001t0005g0269 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-94+3299T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882282 | |||||||
chr10:50882624 | A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(42): Show | 58 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.-94+2957T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882624 | |||||||
chr10:50882740 | C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0022others(58): Show | 72 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-94+2841G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882740 | |||||||
chr10:50882757 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-94+2824A>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882757 | |||||||
chr10:50882847 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-94+2734A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882847 | |||||||
chr10:50882877 | A | G | 3 | a0001c0001t0008g0006a0001c0001t0008g0102a0001c0001t0010g0101 | 5 | HG01192.hp1 HG02258.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+2704T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50882877 | |||||||
chr10:50883049 | A | C | 1 | a0001c0001t0005g0254 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-94+2532T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883049 | |||||||
chr10:50883139 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+2442C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883139 | |||||||
chr10:50883190 | A | C | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+2391T>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883190 | |||||||
chr10:50883278 | T | C | 6 | a0001c0001t0005g0269a0001c0001t0005g0270a0001c0001t0005g0272others(3): Show | 6 | HG02280.hp1 HG03654.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-94+2303A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883278 | |||||||
chr10:50883318 | A | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(209): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-94+2263T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883318 | |||||||
chr10:50883419 | C | T | 47 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(44): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+2162G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883419 | |||||||
chr10:50883461 | T | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(209): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-94+2120A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883461 | |||||||
chr10:50883734 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+1847C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883734 | |||||||
chr10:50883803 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-94+1778G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50883803 | |||||||
chr10:50884062 | A | G | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(261): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-94+1519T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884062 | |||||||
chr10:50884065 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-94+1516G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884065 | |||||||
chr10:50884144 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-94+1437T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884144 | |||||||
chr10:50884203 | A | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+1378T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884203 | |||||||
chr10:50884324 | G | A | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(261): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-94+1257C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884324 | |||||||
chr10:50884559 | A | T | 47 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0070others(44): Show | 60 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.-94+1022T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884559 | |||||||
chr10:50884611 | C | T | 1 | a0001c0001t0029g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-94+970G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884611 | |||||||
chr10:50884712 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-94+869T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884712 | |||||||
chr10:50884716 | T | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(261): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-94+865A>G | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884716 | |||||||
chr10:50884750 | C | T | 1 | a0001c0008t0001g0045 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-94+831G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884750 | |||||||
chr10:50884774 | A | G | 2 | a0001c0001t0003g0035a0001c0001t0003g0253 | 3 | NA18994.hp1 NA19002.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-94+807T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884774 | |||||||
chr10:50884803 | G | A | 4 | a0001c0001t0003g0039a0001c0001t0003g0275a0001c0001t0003g0276others(1): Show | 5 | HG02602.hp2 NA18948.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+778C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884803 | |||||||
chr10:50884853 | C | G | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+728G>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884853 | |||||||
chr10:50884940 | A | G | 1 | a0001c0001t0040g0044 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-94+641T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50884940 | |||||||
chr10:50885001 | T | A | 10 | a0001c0001t0005g0033a0001c0001t0014g0249a0001c0002t0004g0034others(7): Show | 12 | HG01109.hp2 HG01167.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+580A>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885001 | |||||||
chr10:50885072 | G | A | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+509C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885072 | |||||||
chr10:50885137 | A | T | 2 | a0001c0001t0042g0043a0001c0002t0004g0042 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-94+444T>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885137 | |||||||
chr10:50885350 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-94+231G>A | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885350 | |||||||
chr10:50885488 | G | A | 32 | a0001c0001t0001g0268a0001c0001t0003g0035a0001c0001t0003g0038others(29): Show | 42 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-94+93C>T | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885488 | |||||||
chr10:50885574 | A | G | 1 | a0002c0004t0018g0040 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.-94+7T>C | A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 1/12 | chr10 | 50885574 |