Item | Value |
---|---|
geneid | 23500 |
ensemblid | ENSG00000146122.17 |
hgncid | 18143 |
symbol | DAAM2 |
name | dishevelled associated activator of morphogenesis 2 |
refseq_nuc | NM_001201427.2 |
refseq_prot | NP_001188356.1 |
ensembl_nuc | ENST00000274867.9 |
ensembl_prot | ENSP00000274867.4 |
mane_status | MANE Select |
chr | chr6 |
start | 39792376 |
end | 39904869 |
strand | + |
ver | v1.2 |
region | chr6:39792376-39904869 |
region5000 | chr6:39787376-39909869 |
regionname0 | DAAM2_chr6_39792376_39904869 |
regionname5000 | DAAM2_chr6_39787376_39909869 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1068 | 274 | 80 | 49 | 105 | 6 | 32 | 84 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0002 | 0/0 | 1068 | 6 | 0 | 0 | 5 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0003 | 0/0 | 1068 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0004 | 0/0 | 1068 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0005 | 0/0 | 1068 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0006 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0007 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0008 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0009 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0010 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MASRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0011 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0012 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0013 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0014 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0015 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0016 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
a0017 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | MAPRK others(1063): Show |
chr6 | 39787376 | 39909869 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3204 | 94 | 18 | 22 | 30 | 5 | 18 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0002 | 1/0 | 3204 | 46 | 9 | 12 | 16 | 1 | 7 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0003 | 0/0 | 3204 | 38 | 7 | 9 | 20 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0004 | 0/0 | 3204 | 29 | 7 | 1 | 19 | 0 | 2 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0005 | 0/0 | 3204 | 12 | 6 | 0 | 6 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0006 | 0/0 | 3204 | 11 | 8 | 2 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0007 | 0/0 | 3204 | 10 | 0 | 0 | 10 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0008 | 0/0 | 3204 | 8 | 8 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0009 | 0/0 | 3204 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0012 | 0/0 | 3204 | 3 | 1 | 1 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0013 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0014 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0016 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0017 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0022 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0025 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0026 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0031 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0032 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0033 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0036 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0037 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0039 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0042 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0044 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0045 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0001c0046 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0002c0010 | 0/0 | 3204 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0002c0015 | 0/0 | 3204 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0003c0011 | 0/0 | 3204 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0003c0024 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0004c0020 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0004c0030 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0005c0028 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0005c0029 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0006c0040 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0007c0023 | 0/0 | 3204 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0008c0038 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0009c0019 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0010c0047 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0011c0043 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0012c0041 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0013c0034 | 0/0 | 3204 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0014c0021 | 0/0 | 3204 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0015c0027 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0016c0035 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 | ||
a0017c0018 | 0/0 | 3204 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | ATGGC others(3199): Show |
chr6 | 39787376 | 39909869 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6185 | 78 | 14 | 19 | 26 | 2 | 16 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0008 | 0/0 | 6185 | 5 | 0 | 2 | 0 | 2 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0010 | 0/0 | 6189 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0017 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0019 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0025 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0032 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0033 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0001t0036 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0002t0002 | 1/0 | 6185 | 44 | 8 | 11 | 16 | 1 | 7 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0002t0030 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0002t0038 | 0/0 | 6181 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6176): Show |
chr6 | 39787376 | 39909869 |
a0001c0003t0003 | 0/0 | 6189 | 29 | 2 | 6 | 20 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0003t0007 | 0/0 | 6189 | 3 | 0 | 3 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0003t0014 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0003t0016 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0003t0039 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0003 | 0/0 | 6189 | 4 | 2 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0004 | 0/0 | 6189 | 12 | 0 | 0 | 11 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0006 | 0/0 | 6188 | 5 | 0 | 0 | 5 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0007 | 0/0 | 6189 | 2 | 0 | 1 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0012 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0021 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0026 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0031 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0004t0035 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0003 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0004 | 0/0 | 6189 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0006 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0011 | 0/0 | 6185 | 4 | 4 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0014 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0005t0037 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0006t0001 | 0/0 | 6185 | 8 | 5 | 2 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0006t0020 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0006t0027 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0006t0028 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0007t0003 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0007t0012 | 0/0 | 6188 | 3 | 0 | 0 | 3 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0007t0013 | 0/0 | 6188 | 4 | 0 | 0 | 4 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0007t0015 | 0/0 | 6188 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0008t0005 | 0/0 | 6189 | 7 | 7 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0008t0024 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0009t0009 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0009t0029 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0012t0002 | 0/0 | 6185 | 3 | 1 | 1 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0013t0023 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0014t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0014t0017 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0016t0004 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0017t0018 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0022t0020 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0025t0034 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0026t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0031t0040 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0032t0009 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0033t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0036t0022 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0037t0002 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0039t0015 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0001c0042t0002 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0044t0022 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0001c0045t0002 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0001c0046t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0002c0010t0002 | 0/0 | 6185 | 4 | 0 | 0 | 3 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0002c0015t0003 | 0/0 | 6189 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0003c0011t0001 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0003c0024t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0004c0020t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0004c0030t0001 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0005c0028t0004 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0005c0029t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0006c0040t0002 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0007c0023t0007 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0008c0038t0009 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0009c0019t0003 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0010c0047t0001 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0011c0043t0005 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0012c0041t0014 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0013c0034t0001 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0014c0021t0001 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
a0015c0027t0006 | 0/0 | 6188 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6183): Show |
chr6 | 39787376 | 39909869 |
a0016c0035t0003 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6184): Show |
chr6 | 39787376 | 39909869 |
a0017c0018t0018 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | GATAG others(6180): Show |
chr6 | 39787376 | 39909869 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0008g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0019g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0025g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0032g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0033g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0001t0036g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0002g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0030g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0002t0038g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0007g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0007g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0016g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0016g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0003t0039g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0007g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0021g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0021g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0026g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0031g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0004t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0005t0037g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0020g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0027g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0006t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0013g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0013g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0015g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0007t0015g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0008t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0009t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0009t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0009t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0009t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0012t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0012t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0012t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0013t0023g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0013t0023g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0014t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0014t0017g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0016t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0017t0018g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0022t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0025t0034g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0026t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0031t0040g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0032t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0033t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0036t0022g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0037t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0039t0015g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0042t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0044t0022g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0045t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0001c0046t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0010t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0010t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0010t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0010t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0015t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0002c0015t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0003c0011t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0003c0011t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0003c0011t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0003c0024t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0004c0020t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0004c0030t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0005c0028t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0005c0029t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0006c0040t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0007c0023t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0008c0038t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0009c0019t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0010c0047t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0011c0043t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0012c0041t0014g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0013c0034t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0014c0021t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0015c0027t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0016c0035t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
a0017c0018t0018g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0033 | g0225 | EUR | GBR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0157 | EUR | GBR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0218 | EUR | FIN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00423 | hp1 | a0001 | c0003 | t0003 | g0060 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00423 | hp2 | a0001 | c0005 | t0006 | g0199 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00438 | hp1 | a0001 | c0003 | t0003 | g0109 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00438 | hp2 | a0002 | c0015 | t0003 | g0095 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00609 | hp1 | a0001 | c0004 | t0004 | g0196 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00621 | hp1 | a0001 | c0003 | t0003 | g0179 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00735 | hp1 | a0001 | c0004 | t0007 | g0158 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0215 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG00741 | hp2 | a0001 | c0006 | t0001 | g0159 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01074 | hp1 | a0001 | c0003 | t0007 | g0002 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01074 | hp2 | a0001 | c0002 | t0038 | g0130 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01081 | hp1 | a0004 | c0030 | t0001 | g0193 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0150 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01169 | hp2 | a0006 | c0040 | t0002 | g0229 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01175 | hp1 | a0001 | c0003 | t0007 | g0016 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01243 | hp1 | a0001 | c0031 | t0040 | g0143 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0254 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01358 | hp2 | a0001 | c0006 | t0001 | g0015 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01361 | hp2 | a0001 | c0044 | t0022 | g0115 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01433 | hp2 | a0001 | c0003 | t0007 | g0250 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0149 | EUR | IBS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01884 | hp1 | a0001 | c0026 | t0001 | g0279 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01884 | hp2 | a0001 | c0008 | t0005 | g0102 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01891 | hp1 | a0001 | c0013 | t0023 | g0171 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01934 | hp2 | a0007 | c0023 | t0007 | g0232 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0262 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01943 | hp2 | a0001 | c0003 | t0003 | g0259 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0136 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01975 | hp1 | a0001 | c0003 | t0003 | g0036 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01978 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0252 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02004 | hp1 | a0001 | c0001 | t0036 | g0224 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0010 | AMR | PEL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02015 | hp2 | a0002 | c0010 | t0002 | g0255 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02027 | hp1 | a0002 | c0010 | t0002 | g0235 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0104 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02055 | hp1 | a0001 | c0009 | t0009 | g0163 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02055 | hp2 | a0001 | c0008 | t0005 | g0285 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02056 | hp1 | a0002 | c0010 | t0002 | g0096 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02083 | hp2 | a0001 | c0004 | t0004 | g0047 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02129 | hp1 | a0001 | c0004 | t0004 | g0071 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02129 | hp2 | a0002 | c0015 | t0003 | g0217 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0267 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0177 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02257 | hp2 | a0001 | c0004 | t0003 | g0103 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02280 | hp1 | a0001 | c0005 | t0011 | g0125 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02280 | hp2 | a0001 | c0006 | t0001 | g0294 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02451 | hp1 | a0001 | c0004 | t0021 | g0101 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0288 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02523 | hp2 | a0001 | c0001 | t0010 | g0085 | EAS | KHV | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02572 | hp2 | a0001 | c0032 | t0009 | g0169 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02602 | hp1 | a0001 | c0001 | t0010 | g0268 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02615 | hp1 | a0001 | c0008 | t0024 | g0034 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02615 | hp2 | a0009 | c0019 | t0003 | g0037 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02622 | hp1 | a0001 | c0008 | t0005 | g0166 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02630 | hp1 | a0001 | c0009 | t0009 | g0112 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02630 | hp2 | a0001 | c0006 | t0001 | g0033 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0116 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02683 | hp1 | a0010 | c0047 | t0001 | g0067 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02717 | hp1 | a0001 | c0003 | t0016 | g0283 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02735 | hp1 | a0001 | c0004 | t0007 | g0236 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0148 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02809 | hp2 | a0001 | c0002 | t0030 | g0175 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02818 | hp1 | a0001 | c0005 | t0014 | g0176 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02818 | hp2 | a0005 | c0029 | t0001 | g0178 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02886 | hp1 | a0001 | c0036 | t0022 | g0168 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02886 | hp2 | a0001 | c0006 | t0028 | g0188 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02895 | hp1 | a0001 | c0042 | t0002 | g0005 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02895 | hp2 | a0001 | c0006 | t0027 | g0189 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02922 | hp1 | a0003 | c0024 | t0001 | g0029 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02922 | hp2 | a0001 | c0001 | t0017 | g0266 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02965 | hp1 | a0001 | c0005 | t0011 | g0043 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02965 | hp2 | a0001 | c0006 | t0001 | g0191 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02970 | hp1 | a0003 | c0011 | t0001 | g0007 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02976 | hp1 | a0001 | c0004 | t0026 | g0028 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02976 | hp2 | a0001 | c0008 | t0005 | g0278 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0201 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0153 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03041 | hp2 | a0003 | c0011 | t0001 | g0006 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03098 | hp1 | a0001 | c0005 | t0003 | g0291 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03130 | hp1 | a0001 | c0005 | t0011 | g0093 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03130 | hp2 | a0001 | c0014 | t0017 | g0265 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03139 | hp1 | a0001 | c0009 | t0029 | g0174 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03139 | hp2 | a0001 | c0008 | t0005 | g0292 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0041 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03195 | hp2 | a0001 | c0009 | t0009 | g0128 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03209 | hp1 | a0001 | c0008 | t0005 | g0026 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03209 | hp2 | a0001 | c0033 | t0001 | g0045 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03225 | hp1 | a0011 | c0043 | t0005 | g0151 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03225 | hp2 | a0001 | c0014 | t0001 | g0030 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03453 | hp1 | a0001 | c0003 | t0014 | g0087 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0277 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03486 | hp1 | a0004 | c0020 | t0001 | g0276 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03486 | hp2 | a0001 | c0046 | t0001 | g0044 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03491 | hp1 | a0001 | c0045 | t0002 | g0164 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03516 | hp1 | a0003 | c0011 | t0001 | g0004 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03516 | hp2 | a0001 | c0004 | t0021 | g0061 | AFR | ESN | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03540 | hp1 | a0001 | c0001 | t0019 | g0122 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03540 | hp2 | a0001 | c0004 | t0035 | g0126 | AFR | GWD | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03579 | hp2 | a0001 | c0003 | t0003 | g0117 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0238 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03704 | hp1 | a0001 | c0037 | t0002 | g0214 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03704 | hp2 | a0001 | c0006 | t0001 | g0135 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03710 | hp1 | a0012 | c0041 | t0014 | g0147 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0132 | SAS | PJL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03927 | hp2 | a0002 | c0010 | t0002 | g0256 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04184 | hp2 | a0001 | c0004 | t0004 | g0139 | SAS | BEB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04199 | hp2 | a0001 | c0003 | t0039 | g0091 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04228 | hp1 | a0013 | c0034 | t0001 | g0231 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | STU | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0051 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18747 | hp1 | a0001 | c0007 | t0012 | g0079 | EAS | CHB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18747 | hp2 | a0001 | c0003 | t0003 | g0289 | EAS | CHB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18906 | hp1 | a0001 | c0022 | t0020 | g0048 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18939 | hp2 | a0001 | c0004 | t0006 | g0141 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18940 | hp2 | a0001 | c0003 | t0003 | g0069 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18944 | hp1 | a0005 | c0028 | t0004 | g0290 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18944 | hp2 | a0001 | c0007 | t0015 | g0244 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18945 | hp1 | a0001 | c0007 | t0013 | g0208 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18945 | hp2 | a0001 | c0004 | t0006 | g0090 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18949 | hp1 | a0015 | c0027 | t0006 | g0248 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18949 | hp2 | a0001 | c0003 | t0003 | g0155 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18952 | hp2 | a0001 | c0005 | t0004 | g0082 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18954 | hp1 | a0001 | c0004 | t0004 | g0172 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18954 | hp2 | a0001 | c0007 | t0012 | g0080 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18956 | hp1 | a0001 | c0007 | t0013 | g0065 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18956 | hp2 | a0001 | c0004 | t0004 | g0052 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18960 | hp1 | a0001 | c0007 | t0003 | g0059 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18960 | hp2 | a0001 | c0004 | t0004 | g0062 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18963 | hp2 | a0001 | c0001 | t0032 | g0243 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18966 | hp2 | a0001 | c0007 | t0013 | g0245 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18968 | hp2 | a0001 | c0003 | t0003 | g0100 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18970 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18970 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18971 | hp2 | a0001 | c0004 | t0012 | g0099 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18975 | hp2 | a0001 | c0004 | t0006 | g0075 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18981 | hp1 | a0001 | c0007 | t0015 | g0058 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18984 | hp1 | a0001 | c0005 | t0004 | g0050 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18990 | hp2 | a0001 | c0007 | t0012 | g0081 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18993 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18994 | hp1 | a0016 | c0035 | t0003 | g0173 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18994 | hp2 | a0001 | c0016 | t0004 | g0055 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18997 | hp1 | a0001 | c0004 | t0004 | g0197 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18997 | hp2 | a0017 | c0018 | t0018 | g0054 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA18998 | hp2 | a0001 | c0004 | t0006 | g0287 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19002 | hp2 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19007 | hp1 | a0001 | c0004 | t0004 | g0092 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19009 | hp1 | a0001 | c0004 | t0004 | g0056 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19011 | hp2 | a0001 | c0005 | t0004 | g0212 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19030 | hp1 | a0001 | c0003 | t0016 | g0123 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19030 | hp2 | a0001 | c0003 | t0014 | g0211 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19043 | hp1 | a0001 | c0005 | t0011 | g0031 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19060 | hp2 | a0001 | c0039 | t0015 | g0227 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19062 | hp2 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19066 | hp1 | a0001 | c0004 | t0004 | g0206 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19074 | hp2 | a0001 | c0007 | t0013 | g0083 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19077 | hp1 | a0001 | c0005 | t0037 | g0063 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19077 | hp2 | a0001 | c0005 | t0004 | g0064 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19084 | hp1 | a0001 | c0004 | t0006 | g0142 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19084 | hp2 | a0001 | c0012 | t0002 | g0240 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19086 | hp1 | a0001 | c0004 | t0004 | g0038 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19086 | hp2 | a0001 | c0003 | t0003 | g0129 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0111 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19091 | hp1 | a0001 | c0003 | t0003 | g0078 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19091 | hp2 | a0001 | c0017 | t0018 | g0053 | EAS | JPT | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19240 | hp1 | a0001 | c0004 | t0031 | g0293 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA19240 | hp2 | a0001 | c0012 | t0002 | g0297 | AFR | YRI | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | ASW | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20129 | hp2 | a0001 | c0003 | t0016 | g0207 | AFR | ASW | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0263 | SAS | GIH | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01123 | hp1 | a0001 | c0012 | t0002 | g0219 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02109 | hp1 | a0001 | c0008 | t0005 | g0167 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02109 | hp2 | a0008 | c0038 | t0009 | g0042 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02486 | hp2 | a0001 | c0006 | t0020 | g0284 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02559 | hp1 | a0001 | c0013 | t0023 | g0170 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG03471 | hp2 | a0001 | c0001 | t0025 | g0032 | AFR | MSL | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG06807 | hp1 | a0014 | c0021 | t0001 | g0296 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
HG06807 | hp2 | a0001 | c0025 | t0034 | g0299 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | USA | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0257 | REF | REF | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0298 | REF | REF | DAAM2_chr6_39787376_39909869 | DAAM2 | chr6 | 39787376 | 39909869 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:39792463 | G | C | 1 | a0001 | 3 | HG02922.hp2 HG03130.hp2 NA19240.hp1 |
splice_region_variant | LOW | c.-59G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | chr6 | 39792463 | |||||||
chr6:39856309 | C | T | 1 | a0010 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.7C>T | p.Pro3Ser | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 153/6185 | 7/3207 | 3/1068 | chr6 | 39856309 | |||
chr6:39856342 | C | A | 1 | a0009 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.40C>A | p.Leu14Met | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 186/6185 | 40/3207 | 14/1068 | chr6 | 39856342 | |||
chr6:39867596 | G | A | 1 | a0007 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.515G>A | p.Arg172His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 661/6185 | 515/3207 | 172/1068 | chr6 | 39867596 | |||
chr6:39867706 | C | T | 1 | a0014 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.625C>T | p.Arg209Cys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 771/6185 | 625/3207 | 209/1068 | chr6 | 39867706 | |||
chr6:39867814 | G | C | 1 | a0003 | 4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.733G>C | p.Val245Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 879/6185 | 733/3207 | 245/1068 | chr6 | 39867814 | |||
chr6:39867835 | C | T | 1 | a0017 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.754C>T | p.Arg252Cys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/25 | 900/6185 | 754/3207 | 252/1068 | chr6 | 39867835 | |||
chr6:39875341 | G | A | 1 | a0009 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1174G>A | p.Gly392Ser | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/25 | 1320/6185 | 1174/3207 | 392/1068 | chr6 | 39875341 | |||
chr6:39878218 | T | A | 1 | a0015 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1317T>A | p.Asn439Lys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/25 | 1463/6185 | 1317/3207 | 439/1068 | chr6 | 39878218 | |||
chr6:39879350 | C | T | 1 | a0012 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1718C>T | p.Pro573Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1864/6185 | 1718/3207 | 573/1068 | chr6 | 39879350 | |||
chr6:39879422 | G | A | 1 | a0005 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1790G>A | p.Arg597His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1936/6185 | 1790/3207 | 597/1068 | chr6 | 39879422 | |||
chr6:39879422 | G | C | 1 | a0005 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1790G>C | p.Arg597Pro | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1936/6185 | 1790/3207 | 597/1068 | chr6 | 39879422 | |||
chr6:39879431 | A | G | 1 | a0002 | 6 | HG00438.hp2 HG02015.hp2 HG02027.hp1 others(3): Show |
missense_variant | MODERATE | c.1799A>G | p.Gln600Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/25 | 1945/6185 | 1799/3207 | 600/1068 | chr6 | 39879431 | |||
chr6:39883966 | G | A | 2 | a0004 a0014 |
3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1850G>A | p.Arg617His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 1996/6185 | 1850/3207 | 617/1068 | chr6 | 39883966 | |||
chr6:39884038 | A | G | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1922A>G | p.Glu641Gly | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 2068/6185 | 1922/3207 | 641/1068 | chr6 | 39884038 | |||
chr6:39891660 | A | G | 1 | a0016 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.2279A>G | p.Gln760Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/25 | 2425/6185 | 2279/3207 | 760/1068 | chr6 | 39891660 | |||
chr6:39901326 | G | A | 1 | a0006 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.2836G>A | p.Gly946Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 2982/6185 | 2836/3207 | 946/1068 | chr6 | 39901326 | |||
chr6:39901459 | G | T | 1 | a0013 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2969G>T | p.Arg990Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 3115/6185 | 2969/3207 | 990/1068 | chr6 | 39901459 | |||
chr6:39901990 | G | A | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3160G>A | p.Ala1054Thr | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 3306/6185 | 3160/3207 | 1054/1068 | chr6 | 39901990 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:39856329 | T | C | 4 | a0001c0007 a0001c0016 a0001c0017 others(1): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
synonymous_variant | LOW | c.27T>C | p.His9His | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 173/6185 | 27/3207 | 9/1068 | chr6 | 39856329 | |||
chr6:39856353 | C | T | 1 | a0001c0046 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.51C>T | p.Phe17Phe | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 197/6185 | 51/3207 | 17/1068 | chr6 | 39856353 | |||
chr6:39856431 | G | A | 2 | a0004c0020 a0014c0021 |
2 | HG03486.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.129G>A | p.Pro43Pro | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 275/6185 | 129/3207 | 43/1068 | chr6 | 39856431 | |||
chr6:39856434 | C | T | 1 | a0001c0045 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.132C>T | p.Asn44Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 278/6185 | 132/3207 | 44/1068 | chr6 | 39856434 | |||
chr6:39856449 | C | T | 1 | a0001c0044 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.147C>T | p.Asn49Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/25 | 293/6185 | 147/3207 | 49/1068 | chr6 | 39856449 | |||
chr6:39860955 | C | A | 1 | a0001c0022 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.196C>A | p.Arg66Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/25 | 342/6185 | 196/3207 | 66/1068 | chr6 | 39860955 | |||
chr6:39868834 | C | T | 3 | a0001c0008 a0001c0046 a0011c0043 |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
synonymous_variant | LOW | c.774C>T | p.Asn258Asn | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/25 | 920/6185 | 774/3207 | 258/1068 | chr6 | 39868834 | |||
chr6:39875412 | T | C | 3 | a0001c0013 a0001c0025 a0001c0026 |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.1245T>C | p.Gly415Gly | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/25 | 1391/6185 | 1245/3207 | 415/1068 | chr6 | 39875412 | |||
chr6:39878206 | C | T | 1 | a0001c0042 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1305C>T | p.Leu435Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/25 | 1451/6185 | 1305/3207 | 435/1068 | chr6 | 39878206 | |||
chr6:39884042 | G | A | 21 | a0001c0001 a0001c0003 a0001c0004 others(18): Show |
180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
synonymous_variant | LOW | c.1926G>A | p.Lys642Lys | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/25 | 2072/6185 | 1926/3207 | 642/1068 | chr6 | 39884042 | |||
chr6:39887512 | C | A | 12 | a0001c0003 a0001c0008 a0001c0009 others(9): Show |
63 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(60): Show |
synonymous_variant | LOW | c.1980C>A | p.Ile660Ile | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/25 | 2126/6185 | 1980/3207 | 660/1068 | chr6 | 39887512 | |||
chr6:39888745 | T | A | 1 | a0001c0037 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2127T>A | p.Ala709Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/25 | 2273/6185 | 2127/3207 | 709/1068 | chr6 | 39888745 | |||
chr6:39896954 | C | T | 19 | a0001c0001 a0001c0006 a0001c0008 others(16): Show |
131 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
synonymous_variant | LOW | c.2484C>T | p.Ile828Ile | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/25 | 2630/6185 | 2484/3207 | 828/1068 | chr6 | 39896954 | |||
chr6:39897271 | T | C | 40 | a0001c0001 a0001c0003 a0001c0004 others(37): Show |
242 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(239): Show |
synonymous_variant | LOW | c.2607T>C | p.Ala869Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/25 | 2753/6185 | 2607/3207 | 869/1068 | chr6 | 39897271 | |||
chr6:39900178 | G | T | 1 | a0001c0039 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.2781G>T | p.Leu927Leu | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/25 | 2927/6185 | 2781/3207 | 927/1068 | chr6 | 39900178 | |||
chr6:39901457 | G | A | 1 | a0001c0033 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2967G>A | p.Ala989Ala | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/25 | 3113/6185 | 2967/3207 | 989/1068 | chr6 | 39901457 | |||
chr6:39902007 | G | T | 3 | a0001c0009 a0001c0032 a0008c0038 |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.3177G>T | p.Arg1059Arg | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 3323/6185 | 3177/3207 | 1059/1068 | chr6 | 39902007 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:39792399 | G | C | 3 | a0001c0001t0025 a0001c0004t0026 a0001c0008t0024 |
3 | HG02615.hp1 HG02976.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63904 | chr6 | 39792399 | ||||||
chr6:39792444 | C | T | 1 | a0001c0031t0040 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63859 | chr6 | 39792444 | ||||||
chr6:39792455 | G | A | 4 | a0001c0002t0030 a0001c0006t0027 a0001c0006t0028 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63848 | chr6 | 39792455 | ||||||
chr6:39792460 | C | T | 1 | a0001c0003t0039 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/25 | 63843 | chr6 | 39792460 | ||||||
chr6:39902176 | T | A | 36 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(33): Show |
138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*139T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 139 | chr6 | 39902176 | ||||||
chr6:39902237 | T | C | 66 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(63): Show |
229 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*200T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 200 | chr6 | 39902237 | ||||||
chr6:39902253 | C | T | 1 | a0001c0001t0036 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 216 | chr6 | 39902253 | ||||||
chr6:39902426 | G | A | 4 | a0001c0004t0012 a0001c0007t0012 a0001c0017t0018 others(1): Show |
6 | NA18747.hp1 NA18954.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*389G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 389 | chr6 | 39902426 | ||||||
chr6:39902491 | C | A | 2 | a0001c0004t0021 a0001c0004t0031 |
3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*454C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 454 | chr6 | 39902491 | ||||||
chr6:39902563 | A | G | 1 | a0001c0005t0011 | 4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*526A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 526 | chr6 | 39902563 | ||||||
chr6:39902885 | G | A | 1 | a0001c0001t0032 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 848 | chr6 | 39902885 | ||||||
chr6:39902930 | T | A | 2 | a0001c0007t0015 a0001c0039t0015 |
3 | NA18944.hp2 NA18981.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*893T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 893 | chr6 | 39902930 | ||||||
chr6:39902966 | C | T | 4 | a0001c0009t0009 a0001c0009t0029 a0001c0032t0009 others(1): Show |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*929C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 929 | chr6 | 39902966 | ||||||
chr6:39902971 | C | G | 2 | a0001c0007t0015 a0001c0039t0015 |
3 | NA18944.hp2 NA18981.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*934C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 934 | chr6 | 39902971 | ||||||
chr6:39902975 | G | C | 1 | a0001c0001t0033 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 938 | chr6 | 39902975 | ||||||
chr6:39903264 | G | A | 1 | a0001c0013t0023 | 2 | HG01891.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1227 | chr6 | 39903264 | ||||||
chr6:39903435 | T | C | 1 | a0001c0001t0019 | 2 | HG03540.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1398 | chr6 | 39903435 | ||||||
chr6:39903629 | AC | A | 5 | a0001c0004t0012 a0001c0007t0012 a0001c0007t0013 others(2): Show |
11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1594delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1594 | INFO_REALIGN_3_PRIME | chr6 | 39903629 | |||||
chr6:39903748 | CG | C | 3 | a0001c0004t0006 a0001c0005t0006 a0015c0027t0006 |
7 | HG00423.hp2 NA18939.hp2 NA18945.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1718delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1718 | INFO_REALIGN_3_PRIME | chr6 | 39903748 | |||||
chr6:39903749 | G | A | 5 | a0001c0004t0021 a0001c0004t0031 a0001c0006t0020 others(2): Show |
6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1712G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1712 | chr6 | 39903749 | ||||||
chr6:39903751 | G | T | 4 | a0001c0003t0007 a0001c0004t0007 a0001c0004t0035 others(1): Show |
7 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1714G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1714 | chr6 | 39903751 | ||||||
chr6:39903756 | A | G | 8 | a0001c0003t0007 a0001c0003t0014 a0001c0003t0039 others(5): Show |
12 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1719A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1719 | chr6 | 39903756 | ||||||
chr6:39903831 | A | G | 2 | a0001c0036t0022 a0001c0044t0022 |
2 | HG01361.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1794A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 1794 | chr6 | 39903831 | ||||||
chr6:39904168 | T | C | 5 | a0001c0004t0021 a0001c0004t0031 a0001c0006t0020 others(2): Show |
6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2131T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2131 | chr6 | 39904168 | ||||||
chr6:39904325 | C | G | 1 | a0001c0025t0034 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2288C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2288 | chr6 | 39904325 | ||||||
chr6:39904429 | G | C | 5 | a0001c0004t0021 a0001c0004t0031 a0001c0006t0020 others(2): Show |
6 | HG02451.hp1 HG02486.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2392G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2392 | chr6 | 39904429 | ||||||
chr6:39904448 | T | C | 3 | a0001c0008t0005 a0001c0008t0024 a0011c0043t0005 |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2411T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2411 | chr6 | 39904448 | ||||||
chr6:39904464 | C | G | 1 | a0001c0001t0008 | 5 | HG00323.hp2 HG00741.hp1 HG01081.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2427C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2427 | chr6 | 39904464 | ||||||
chr6:39904578 | G | GAAAT | 40 | a0001c0001t0010 a0001c0003t0003 a0001c0003t0007 others(37): Show |
111 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2545_*2548dupTAAA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2549 | INFO_REALIGN_3_PRIME | chr6 | 39904578 | |||||
chr6:39904689 | ACTAT | A | 6 | a0001c0002t0038 a0001c0004t0021 a0001c0004t0031 others(3): Show |
7 | HG01074.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2659_*2662delATCT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2659 | INFO_REALIGN_3_PRIME | chr6 | 39904689 | |||||
chr6:39904728 | C | A | 28 | a0001c0001t0010 a0001c0003t0003 a0001c0003t0007 others(25): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2691C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 25/25 | 2691 | chr6 | 39904728 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:39792545 | T | C | 1 | a0001c0003t0007g0002 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-57+80T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792545 | |||||||
chr6:39792570 | C | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+105C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792570 | |||||||
chr6:39792670 | G | C | 295 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(292): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+205G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792670 | |||||||
chr6:39792716 | T | G | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
23 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+251T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792716 | |||||||
chr6:39792797 | G | A | 9 | a0001c0001t0025g0032 a0001c0002t0002g0027 a0001c0004t0026g0028 others(6): Show |
9 | HG02615.hp1 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+332G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792797 | |||||||
chr6:39792849 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+384T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792849 | |||||||
chr6:39792937 | G | A | 1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-57+472G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792937 | |||||||
chr6:39792938 | C | A | 1 | a0009c0019t0003g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+473C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792938 | |||||||
chr6:39792942 | T | C | 1 | a0001c0008t0005g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+477T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792942 | |||||||
chr6:39792965 | A | G | 221 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-57+500A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39792965 | |||||||
chr6:39793137 | G | A | 1 | a0001c0003t0003g0111 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-57+672G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793137 | |||||||
chr6:39793187 | G | C | 1 | a0001c0009t0009g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+722G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793187 | |||||||
chr6:39793332 | A | G | 1 | a0001c0002t0002g0295 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-57+867A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793332 | |||||||
chr6:39793372 | G | A | 1 | a0001c0004t0004g0038 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-57+907G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793372 | |||||||
chr6:39793408 | C | A | 1 | a0001c0003t0003g0003 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-57+943C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793408 | |||||||
chr6:39793551 | TC | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+1089delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39793551 | ||||||
chr6:39793561 | C | T | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+1096C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793561 | |||||||
chr6:39793749 | G | T | 5 | a0001c0003t0003g0286 a0001c0003t0003g0288 a0001c0003t0003g0289 others(2): Show |
5 | HG02083.hp1 HG02523.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+1284G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793749 | |||||||
chr6:39793820 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+1355G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793820 | |||||||
chr6:39793960 | T | A | 2 | a0001c0002t0002g0114 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57+1495T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793960 | |||||||
chr6:39793995 | G | T | 11 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0002g0277 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+1530G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39793995 | |||||||
chr6:39794165 | G | A | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+1700G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794165 | |||||||
chr6:39794438 | G | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+1973G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794438 | |||||||
chr6:39794568 | A | G | 2 | a0001c0002t0002g0275 a0004c0020t0001g0276 |
2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-57+2103A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794568 | |||||||
chr6:39794726 | C | G | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-57+2261C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794726 | |||||||
chr6:39794797 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+2332G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794797 | |||||||
chr6:39794884 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
32 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+2419C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794884 | |||||||
chr6:39794903 | C | A | 3 | a0001c0003t0003g0117 a0001c0004t0003g0116 a0009c0019t0003g0037 |
3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+2438C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39794903 | |||||||
chr6:39795206 | T | A | 7 | a0001c0001t0001g0040 a0001c0002t0002g0039 a0001c0005t0011g0043 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+2741T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795206 | |||||||
chr6:39795291 | C | T | 11 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0010g0268 others(8): Show |
11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+2826C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795291 | |||||||
chr6:39795292 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
20 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+2827G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795292 | |||||||
chr6:39795348 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+2883A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795348 | |||||||
chr6:39795419 | G | C | 11 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0010g0268 others(8): Show |
11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+2954G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795419 | |||||||
chr6:39795439 | G | A | 1 | a0001c0002t0002g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-57+2974G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795439 | |||||||
chr6:39795519 | C | T | 2 | a0001c0001t0017g0266 a0001c0014t0017g0265 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+3054C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795519 | |||||||
chr6:39795730 | T | C | 107 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
107 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.-57+3265T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39795730 | |||||||
chr6:39796008 | C | T | 3 | a0001c0001t0001g0264 a0001c0002t0002g0262 a0001c0002t0002g0263 |
3 | HG00735.hp2 HG01943.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-57+3543C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796008 | |||||||
chr6:39796500 | G | A | 2 | a0001c0001t0017g0266 a0001c0014t0017g0265 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+4035G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796500 | |||||||
chr6:39796548 | T | C | 1 | a0001c0004t0003g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-57+4083T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796548 | |||||||
chr6:39796594 | T | C | 1 | a0001c0004t0004g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-57+4129T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796594 | |||||||
chr6:39796619 | C | CA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
31 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+4176dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CA | C | 25 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0113 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.-57+4176delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CAA | C | 81 | a0001c0001t0001g0190 a0001c0001t0001g0194 a0001c0001t0001g0195 others(78): Show |
82 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-57+4175_-57+4176d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CAAA | C | 13 | a0001c0001t0001g0258 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG01943.hp2 HG02083.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+4174_-57+4176d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CAAAAA | C | 51 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(48): Show |
51 | HG00099.hp2 HG00735.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.-57+4172_-57+4176d others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CAAAAAA | C | 13 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0002g0277 others(10): Show |
13 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+4171_-57+4176d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796619 | CAAAAAAA | C | 8 | a0001c0008t0005g0167 a0001c0013t0023g0170 a0001c0013t0023g0171 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+4170_-57+4176d others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796619 | ||||||
chr6:39796646 | TA | T | 211 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(208): Show |
212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-57+4191delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39796646 | ||||||
chr6:39796881 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+4416T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796881 | |||||||
chr6:39796930 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-57+4465T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796930 | |||||||
chr6:39796957 | C | T | 5 | a0001c0008t0005g0167 a0001c0013t0023g0170 a0001c0013t0023g0171 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4492C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796957 | |||||||
chr6:39796958 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+4493G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39796958 | |||||||
chr6:39797443 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+4978A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797443 | |||||||
chr6:39797575 | G | A | 5 | a0001c0001t0001g0194 a0001c0002t0002g0192 a0001c0003t0003g0177 others(2): Show |
5 | HG01081.hp1 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+5110G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797575 | |||||||
chr6:39797617 | C | T | 6 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0003t0003g0252 others(3): Show |
6 | HG01257.hp1 HG01943.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+5152C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797617 | |||||||
chr6:39797640 | G | C | 1 | a0001c0004t0031g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+5175G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797640 | |||||||
chr6:39797701 | C | G | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
31 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+5236C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797701 | |||||||
chr6:39797903 | A | G | 2 | a0001c0001t0001g0251 a0001c0003t0007g0250 |
2 | HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-57+5438A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797903 | |||||||
chr6:39797921 | A | G | 6 | a0001c0002t0002g0114 a0001c0042t0002g0005 a0001c0044t0022g0115 others(3): Show |
6 | HG01361.hp2 HG02895.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+5456A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39797921 | |||||||
chr6:39798004 | G | A | 1 | a0001c0001t0019g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+5539G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798004 | |||||||
chr6:39798016 | C | T | 2 | a0001c0005t0003g0291 a0001c0005t0014g0176 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+5551C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798016 | |||||||
chr6:39798137 | G | C | 11 | a0001c0002t0002g0114 a0001c0008t0005g0167 a0001c0013t0023g0170 others(8): Show |
11 | HG01361.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+5672G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798137 | |||||||
chr6:39798213 | G | A | 2 | a0001c0008t0005g0167 a0001c0036t0022g0168 |
2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-57+5748G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798213 | |||||||
chr6:39798279 | C | T | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+5814C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798279 | |||||||
chr6:39798302 | A | G | 3 | a0001c0001t0001g0165 a0001c0009t0009g0163 a0001c0045t0002g0164 |
3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+5837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798302 | |||||||
chr6:39798415 | A | T | 4 | a0001c0042t0002g0005 a0003c0011t0001g0004 a0003c0011t0001g0006 others(1): Show |
4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+5950A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798415 | |||||||
chr6:39798672 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+6207A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798672 | |||||||
chr6:39798768 | G | T | 5 | a0001c0008t0005g0167 a0001c0013t0023g0170 a0001c0013t0023g0171 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+6303G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798768 | |||||||
chr6:39798871 | AC | A | 59 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(56): Show |
59 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-57+6407delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39798871 | |||||||
chr6:39799053 | A | T | 3 | a0001c0003t0016g0283 a0001c0006t0020g0284 a0001c0008t0005g0285 |
3 | HG02055.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-57+6588A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799053 | |||||||
chr6:39799062 | G | A | 11 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+6597G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799062 | |||||||
chr6:39799064 | G | T | 4 | a0001c0005t0011g0043 a0001c0033t0001g0045 a0001c0046t0001g0044 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+6599G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799064 | |||||||
chr6:39799251 | A | C | 1 | a0001c0009t0009g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+6786A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799251 | |||||||
chr6:39799286 | G | T | 3 | a0001c0001t0001g0118 a0001c0001t0019g0122 a0001c0003t0016g0123 |
3 | HG02572.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+6821G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799286 | |||||||
chr6:39799300 | T | C | 1 | a0009c0019t0003g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+6835T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799300 | |||||||
chr6:39799361 | C | T | 105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
105 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.-57+6896C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799361 | |||||||
chr6:39799411 | G | A | 1 | a0001c0005t0014g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-57+6946G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799411 | |||||||
chr6:39799421 | G | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+6956G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799421 | |||||||
chr6:39799448 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-57+6983A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799448 | |||||||
chr6:39799466 | T | G | 11 | a0001c0002t0002g0114 a0001c0008t0005g0167 a0001c0013t0023g0170 others(8): Show |
11 | HG01361.hp2 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+7001T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799466 | |||||||
chr6:39799481 | G | A | 1 | a0001c0004t0004g0172 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57+7016G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799481 | |||||||
chr6:39799514 | A | C | 2 | a0001c0002t0002g0114 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-57+7049A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799514 | |||||||
chr6:39799535 | T | C | 95 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(92): Show |
95 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-57+7070T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799535 | |||||||
chr6:39799762 | C | A | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+7297C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799762 | |||||||
chr6:39799767 | G | A | 5 | a0001c0008t0005g0167 a0001c0013t0023g0170 a0001c0013t0023g0171 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7302G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799767 | |||||||
chr6:39799964 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+7499A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39799964 | |||||||
chr6:39800229 | G | T | 103 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(100): Show |
104 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-57+7764G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800229 | |||||||
chr6:39800233 | T | C | 1 | a0001c0002t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+7768T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800233 | |||||||
chr6:39800247 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0019g0122 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+7782G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800247 | |||||||
chr6:39800493 | A | G | 3 | a0001c0001t0001g0165 a0001c0009t0009g0163 a0001c0045t0002g0164 |
3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+8028A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800493 | |||||||
chr6:39800631 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-57+8166G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800631 | |||||||
chr6:39800639 | G | A | 1 | a0004c0020t0001g0276 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+8174G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800639 | |||||||
chr6:39800660 | C | T | 6 | a0001c0002t0030g0175 a0001c0005t0003g0291 a0001c0005t0014g0176 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+8195C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800660 | |||||||
chr6:39800743 | G | A | 1 | a0001c0002t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+8278G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800743 | |||||||
chr6:39800743 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+8278G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800743 | |||||||
chr6:39800763 | C | T | 5 | a0001c0002t0002g0160 a0001c0042t0002g0005 a0003c0011t0001g0004 others(2): Show |
5 | HG01123.hp2 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8298C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39800763 | |||||||
chr6:39801153 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0019g0051 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-57+8688A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801153 | |||||||
chr6:39801218 | A | G | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+8753A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801218 | |||||||
chr6:39801296 | C | T | 1 | a0001c0006t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57+8831C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801296 | |||||||
chr6:39801495 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+9030C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801495 | |||||||
chr6:39801528 | T | C | 106 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(103): Show |
106 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.-57+9063T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801528 | |||||||
chr6:39801609 | T | C | 209 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+9144T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801609 | |||||||
chr6:39801679 | C | T | 104 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(101): Show |
105 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-57+9214C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801679 | |||||||
chr6:39801809 | G | C | 3 | a0001c0001t0001g0118 a0001c0001t0019g0122 a0001c0003t0016g0123 |
3 | HG02572.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+9344G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801809 | |||||||
chr6:39801813 | A | G | 1 | a0001c0003t0003g0104 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-57+9348A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801813 | |||||||
chr6:39801818 | T | C | 209 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+9353T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801818 | |||||||
chr6:39801853 | A | C | 2 | a0001c0001t0001g0165 a0001c0045t0002g0164 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+9388A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801853 | |||||||
chr6:39801861 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
20 | HG00323.hp1 HG01175.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+9396G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39801861 | |||||||
chr6:39802027 | A | T | 209 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(206): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-57+9562A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802027 | |||||||
chr6:39802166 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+9701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802166 | |||||||
chr6:39802388 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0019g0122 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+9923G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802388 | |||||||
chr6:39802597 | C | G | 3 | a0001c0001t0001g0025 a0001c0002t0002g0157 a0001c0004t0007g0158 |
3 | HG00099.hp2 HG00735.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-57+10132C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802597 | |||||||
chr6:39802666 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-57+10201G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802666 | |||||||
chr6:39802769 | A | G | 2 | a0001c0002t0002g0039 a0001c0006t0001g0041 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-57+10304A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802769 | |||||||
chr6:39802775 | G | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-57+10310G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802775 | |||||||
chr6:39802834 | C | T | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+10369C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802834 | |||||||
chr6:39802865 | C | T | 11 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0010g0268 others(8): Show |
11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+10400C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39802865 | |||||||
chr6:39803096 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0019g0122 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+10631G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803096 | |||||||
chr6:39803180 | G | A | 212 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-57+10715G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803180 | |||||||
chr6:39803194 | A | G | 6 | a0001c0002t0002g0114 a0001c0042t0002g0005 a0001c0044t0022g0115 others(3): Show |
6 | HG01361.hp2 HG02895.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+10729A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803194 | |||||||
chr6:39803394 | G | T | 6 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0002g0277 others(3): Show |
6 | HG01884.hp1 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10929G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803394 | |||||||
chr6:39803478 | A | G | 1 | a0001c0002t0002g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-57+11013A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803478 | |||||||
chr6:39803514 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-57+11049T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803514 | |||||||
chr6:39803664 | T | G | 9 | a0001c0002t0002g0114 a0001c0013t0023g0170 a0001c0013t0023g0171 others(6): Show |
9 | HG01361.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+11199T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803664 | |||||||
chr6:39803764 | G | T | 2 | a0001c0001t0001g0113 a0001c0009t0009g0112 |
2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+11299G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803764 | |||||||
chr6:39803831 | C | A | 1 | a0001c0002t0002g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-57+11366C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803831 | |||||||
chr6:39803836 | T | C | 1 | a0001c0003t0016g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+11371T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803836 | |||||||
chr6:39803938 | G | C | 1 | a0001c0009t0009g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+11473G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803938 | |||||||
chr6:39803968 | T | C | 3 | a0001c0001t0001g0165 a0001c0009t0009g0163 a0001c0045t0002g0164 |
3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+11503T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39803968 | |||||||
chr6:39804039 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-57+11574C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804039 | |||||||
chr6:39804065 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+11600G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804065 | |||||||
chr6:39804180 | C | T | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-57+11715C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804180 | |||||||
chr6:39804208 | C | T | 2 | a0001c0001t0001g0023 a0001c0002t0002g0022 |
2 | HG00323.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-57+11743C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804208 | |||||||
chr6:39804258 | C | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-57+11793C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804258 | |||||||
chr6:39804349 | G | A | 11 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0002g0277 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+11884G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804349 | |||||||
chr6:39804371 | CTGTA | C | 14 | a0001c0001t0001g0165 a0001c0001t0001g0280 a0001c0001t0001g0281 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+11912_-57+1191 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804371 | ||||||
chr6:39804447 | A | G | 2 | a0001c0001t0001g0113 a0001c0009t0009g0112 |
2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+11982A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804447 | |||||||
chr6:39804522 | C | CTG | 90 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0035 others(87): Show |
90 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-57+12087_-57+1208 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804522 | C | CTGTG | 54 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0181 others(51): Show |
55 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-57+12085_-57+1208 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804522 | C | CTGTGTG | 26 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0200 others(23): Show |
26 | HG00423.hp2 HG00621.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-57+12083_-57+1208 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804522 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0118 a0001c0001t0001g0202 a0001c0001t0001g0258 others(4): Show |
7 | HG02572.hp1 HG02738.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+12081_-57+1208 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804522 | CTG | C | 16 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0010g0268 others(13): Show |
16 | HG01891.hp1 HG02083.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57+12087_-57+1208 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804522 | CTGTG | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(8): Show |
11 | HG01255.hp1 HG01358.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+12085_-57+1208 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804522 | ||||||
chr6:39804583 | G | A | 1 | a0001c0004t0026g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57+12118G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804583 | |||||||
chr6:39804677 | T | A | 218 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-57+12212T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804677 | |||||||
chr6:39804692 | C | T | 2 | a0001c0004t0021g0101 a0001c0008t0005g0102 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-57+12227C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804692 | |||||||
chr6:39804754 | GTGGTACC others(4): Show |
G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12292_-57+1230 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804754 | ||||||
chr6:39804769 | A | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12304A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804769 | |||||||
chr6:39804770 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12305G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804770 | |||||||
chr6:39804778 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12313G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804778 | |||||||
chr6:39804779 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12314A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804779 | |||||||
chr6:39804781 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12316G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804781 | |||||||
chr6:39804782 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12317G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804782 | |||||||
chr6:39804788 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12323A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804788 | |||||||
chr6:39804791 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12326A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804791 | |||||||
chr6:39804793 | A | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12328A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804793 | |||||||
chr6:39804797 | A | C | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12332A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804797 | |||||||
chr6:39804799 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12334A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804799 | |||||||
chr6:39804800 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12335G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804800 | |||||||
chr6:39804801 | T | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12336T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804801 | |||||||
chr6:39804802 | G | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12337G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804802 | |||||||
chr6:39804803 | C | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12338C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804803 | |||||||
chr6:39804810 | C | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12345C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804810 | |||||||
chr6:39804831 | T | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12366T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804831 | |||||||
chr6:39804834 | T | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12369T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804834 | |||||||
chr6:39804838 | T | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12373T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804838 | |||||||
chr6:39804842 | A | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12377A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804842 | |||||||
chr6:39804850 | T | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12385T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804850 | |||||||
chr6:39804863 | A | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12398A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804863 | |||||||
chr6:39804868 | C | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12403C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804868 | |||||||
chr6:39804883 | G | A | 3 | a0001c0001t0001g0107 a0001c0017t0018g0053 a0017c0018t0018g0054 |
3 | NA18988.hp2 NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-57+12418G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804883 | |||||||
chr6:39804915 | T | C | 2 | a0001c0001t0001g0165 a0001c0045t0002g0164 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+12450T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804915 | |||||||
chr6:39804923 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12458A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804923 | |||||||
chr6:39804928 | G | GGTCTGGT others(26): Show |
1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12465_-57+1246 others(37): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39804928 | ||||||
chr6:39804943 | C | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12478C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804943 | |||||||
chr6:39804947 | C | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12482C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804947 | |||||||
chr6:39804948 | A | C | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12483A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804948 | |||||||
chr6:39804949 | C | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12484C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804949 | |||||||
chr6:39804964 | T | C | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12499T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804964 | |||||||
chr6:39804980 | TGACTGCA others(14): Show |
T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12516_-57+1253 others(25): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39804980 | |||||||
chr6:39805005 | T | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12540T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805005 | |||||||
chr6:39805009 | T | A | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12544T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805009 | |||||||
chr6:39805033 | G | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12568G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805033 | |||||||
chr6:39805034 | A | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12569A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805034 | |||||||
chr6:39805035 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12570A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805035 | |||||||
chr6:39805037 | C | G | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12572C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805037 | |||||||
chr6:39805038 | A | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-57+12573A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805038 | |||||||
chr6:39805105 | A | G | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+12640A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805105 | |||||||
chr6:39805117 | G | A | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+12652G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805117 | |||||||
chr6:39805221 | C | G | 3 | a0001c0003t0003g0117 a0001c0004t0003g0116 a0009c0019t0003g0037 |
3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+12756C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805221 | |||||||
chr6:39805297 | T | A | 106 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(103): Show |
107 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-57+12832T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805297 | |||||||
chr6:39805407 | A | G | 1 | a0001c0004t0007g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-57+12942A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805407 | |||||||
chr6:39805557 | A | AT | 13 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0247 others(10): Show |
13 | HG01361.hp2 HG01891.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+13107dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39805557 | ||||||
chr6:39805557 | AT | A | 55 | a0001c0001t0001g0025 a0001c0001t0001g0113 a0001c0001t0001g0124 others(52): Show |
55 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.-57+13107delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39805557 | ||||||
chr6:39805617 | C | G | 1 | a0001c0005t0011g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+13152C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805617 | |||||||
chr6:39805715 | C | T | 1 | a0001c0006t0001g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-57+13250C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805715 | |||||||
chr6:39805841 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+13376C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805841 | |||||||
chr6:39805908 | C | T | 1 | a0001c0005t0011g0125 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+13443C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39805908 | |||||||
chr6:39806030 | G | C | 1 | a0001c0016t0004g0055 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-57+13565G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806030 | |||||||
chr6:39806197 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-57+13732C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806197 | |||||||
chr6:39806515 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57+14050C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806515 | |||||||
chr6:39806686 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+14221C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806686 | |||||||
chr6:39806792 | C | T | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0032t0009g0169 |
3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+14327C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806792 | |||||||
chr6:39806840 | C | CA | 10 | a0001c0001t0001g0107 a0001c0003t0003g0057 a0001c0003t0003g0060 others(7): Show |
10 | HG00423.hp1 HG02818.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+14390dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39806840 | ||||||
chr6:39806854 | AAG | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0280 a0001c0001t0001g0281 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+14391_-57+1439 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39806854 | ||||||
chr6:39806855 | AG | A | 182 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.-57+14391delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806855 | |||||||
chr6:39806856 | G | A | 13 | a0001c0001t0001g0181 a0001c0001t0001g0222 a0001c0001t0001g0251 others(10): Show |
13 | HG00642.hp2 HG01175.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+14391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806856 | |||||||
chr6:39806917 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+14452A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806917 | |||||||
chr6:39806967 | C | T | 1 | a0001c0004t0012g0099 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-57+14502C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39806967 | |||||||
chr6:39807183 | C | T | 3 | a0001c0006t0001g0153 a0001c0006t0001g0159 a0001c0008t0005g0166 |
3 | HG00741.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57+14718C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807183 | |||||||
chr6:39807188 | C | CA | 9 | a0001c0001t0001g0213 a0001c0001t0001g0273 a0001c0002t0002g0253 others(6): Show |
9 | HG00741.hp2 HG01981.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+14737dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | ||||||
chr6:39807188 | CA | C | 115 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(112): Show |
115 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-57+14737delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | ||||||
chr6:39807188 | CAA | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0113 a0001c0001t0019g0051 others(5): Show |
8 | HG01891.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+14736_-57+1473 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39807188 | ||||||
chr6:39807199 | A | G | 2 | a0001c0001t0017g0266 a0001c0014t0017g0265 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+14734A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807199 | |||||||
chr6:39807205 | G | A | 64 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
64 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-57+14740G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807205 | |||||||
chr6:39807239 | A | T | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0026t0001g0279 |
3 | HG01884.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+14774A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807239 | |||||||
chr6:39807371 | C | A | 2 | a0001c0001t0017g0266 a0001c0014t0017g0265 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+14906C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807371 | |||||||
chr6:39807458 | A | G | 207 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(204): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-57+14993A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807458 | |||||||
chr6:39807479 | G | A | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0032t0009g0169 |
3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+15014G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807479 | |||||||
chr6:39807532 | T | C | 1 | a0001c0004t0004g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-57+15067T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807532 | |||||||
chr6:39807541 | G | C | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+15076G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807541 | |||||||
chr6:39807578 | G | A | 15 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0010g0268 others(12): Show |
15 | HG02083.hp1 HG02109.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.-57+15113G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807578 | |||||||
chr6:39807603 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-57+15138G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807603 | |||||||
chr6:39807828 | T | C | 4 | a0001c0042t0002g0005 a0003c0011t0001g0004 a0003c0011t0001g0006 others(1): Show |
4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+15363T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807828 | |||||||
chr6:39807874 | G | C | 1 | a0001c0008t0005g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+15409G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39807874 | |||||||
chr6:39808039 | A | G | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+15574A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808039 | |||||||
chr6:39808075 | C | CT | 9 | a0001c0001t0001g0097 a0001c0001t0001g0213 a0001c0001t0001g0258 others(6): Show |
9 | HG00423.hp1 HG01891.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+15626dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | ||||||
chr6:39808075 | CT | C | 8 | a0001c0001t0008g0215 a0001c0001t0017g0266 a0001c0002t0002g0237 others(5): Show |
8 | HG00741.hp1 HG01361.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+15626delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | ||||||
chr6:39808075 | CTT | C | 72 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-57+15625_-57+1562 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39808075 | ||||||
chr6:39808100 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+15635C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808100 | |||||||
chr6:39808177 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-57+15712A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808177 | |||||||
chr6:39808404 | A | G | 110 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(107): Show |
111 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+15939A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808404 | |||||||
chr6:39808498 | C | T | 1 | a0001c0006t0001g0015 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-57+16033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808498 | |||||||
chr6:39808584 | C | A | 192 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0035 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-57+16119C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808584 | |||||||
chr6:39808613 | G | A | 1 | a0002c0015t0003g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-57+16148G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808613 | |||||||
chr6:39808620 | C | T | 3 | a0001c0003t0016g0283 a0001c0006t0020g0284 a0001c0008t0005g0285 |
3 | HG02055.hp2 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-57+16155C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808620 | |||||||
chr6:39808773 | G | T | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+16308G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808773 | |||||||
chr6:39808893 | A | C | 1 | a0001c0002t0002g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57+16428A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808893 | |||||||
chr6:39808996 | A | G | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0032t0009g0169 |
3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+16531A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39808996 | |||||||
chr6:39809103 | C | G | 3 | a0001c0003t0003g0117 a0001c0004t0003g0116 a0009c0019t0003g0037 |
3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-57+16638C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809103 | |||||||
chr6:39809259 | G | A | 1 | a0001c0003t0003g0104 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-57+16794G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809259 | |||||||
chr6:39809362 | C | T | 1 | a0001c0002t0002g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-57+16897C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809362 | |||||||
chr6:39809434 | C | T | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+16969C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809434 | |||||||
chr6:39809435 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+16970G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809435 | |||||||
chr6:39809595 | G | T | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0032t0009g0169 |
3 | HG01891.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-57+17130G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809595 | |||||||
chr6:39809668 | A | G | 3 | a0001c0001t0001g0165 a0001c0009t0009g0163 a0001c0045t0002g0164 |
3 | HG02055.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+17203A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809668 | |||||||
chr6:39809939 | C | G | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
90 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-57+17474C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39809939 | |||||||
chr6:39810116 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+17651G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810116 | |||||||
chr6:39810131 | T | C | 2 | a0001c0001t0017g0266 a0001c0014t0017g0265 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-57+17666T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810131 | |||||||
chr6:39810461 | T | G | 294 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(291): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-57+17996T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810461 | |||||||
chr6:39810635 | G | A | 216 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-57+18170G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810635 | |||||||
chr6:39810733 | G | A | 1 | a0001c0002t0002g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-57+18268G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810733 | |||||||
chr6:39810742 | T | G | 1 | a0001c0004t0004g0056 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-57+18277T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810742 | |||||||
chr6:39810838 | A | G | 2 | a0001c0002t0002g0295 a0001c0003t0003g0198 |
2 | NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-57+18373A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810838 | |||||||
chr6:39810863 | C | T | 1 | a0001c0001t0017g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+18398C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39810863 | |||||||
chr6:39811033 | A | G | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+18568A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811033 | |||||||
chr6:39811174 | A | AGT | 55 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0068 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.-57+18747_-57+1874 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | A | AGTAT | 4 | a0001c0002t0030g0175 a0001c0006t0027g0189 a0001c0006t0028g0188 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+18711_-57+1871 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | A | AGTGT | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0152 others(13): Show |
16 | HG00438.hp2 HG02602.hp1 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+18745_-57+1874 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | A | AGTGTGT | 16 | a0001c0001t0001g0105 a0001c0001t0001g0165 a0001c0001t0001g0234 others(13): Show |
16 | HG02056.hp1 HG02083.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+18743_-57+1874 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | A | AGTGTGTG others(1): Show |
10 | a0001c0001t0001g0113 a0001c0001t0001g0271 a0001c0002t0002g0024 others(7): Show |
10 | HG02280.hp2 HG02486.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+18741_-57+1874 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | A | AGTGTGTG others(3): Show |
7 | a0001c0001t0017g0266 a0001c0002t0002g0020 a0001c0002t0002g0021 others(4): Show |
7 | HG02055.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+18739_-57+1874 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | AGT | A | 10 | a0001c0002t0002g0108 a0001c0003t0003g0129 a0001c0004t0031g0293 others(7): Show |
10 | HG01358.hp2 HG01361.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57+18747_-57+1874 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | AGTGT | A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
30 | HG00323.hp1 HG00621.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+18745_-57+1874 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0001g0233 a0007c0023t0007g0232 |
2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+18735_-57+1874 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811174 | AGTGTGTG others(9): Show |
A | 85 | a0001c0001t0001g0035 a0001c0001t0001g0181 a0001c0001t0001g0182 others(82): Show |
86 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.-57+18733_-57+1874 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39811174 | ||||||
chr6:39811466 | A | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0003t0007g0016 |
3 | HG01175.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-57+19001A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811466 | |||||||
chr6:39811488 | T | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(16): Show |
19 | HG00323.hp1 HG00621.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+19023T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811488 | |||||||
chr6:39811528 | C | T | 6 | a0001c0001t0001g0194 a0001c0002t0002g0192 a0001c0003t0003g0177 others(3): Show |
6 | HG01081.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+19063C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811528 | |||||||
chr6:39811549 | G | A | 48 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0131 others(45): Show |
48 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.-57+19084G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811549 | |||||||
chr6:39811564 | C | A | 2 | a0001c0001t0019g0122 a0001c0003t0016g0123 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-57+19099C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811564 | |||||||
chr6:39811750 | A | C | 241 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.-57+19285A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811750 | |||||||
chr6:39811819 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+19354C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811819 | |||||||
chr6:39811940 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-57+19475C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811940 | |||||||
chr6:39811955 | T | A | 1 | a0001c0002t0038g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-57+19490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811955 | |||||||
chr6:39811956 | G | T | 4 | a0001c0042t0002g0005 a0003c0011t0001g0004 a0003c0011t0001g0006 others(1): Show |
4 | HG02895.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+19491G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39811956 | |||||||
chr6:39812050 | G | T | 63 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(60): Show |
63 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-57+19585G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812050 | |||||||
chr6:39812086 | A | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(91): Show |
94 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-57+19621A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812086 | |||||||
chr6:39812128 | C | T | 37 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0001g0134 others(34): Show |
37 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.-57+19663C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812128 | |||||||
chr6:39812339 | C | G | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+19874C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812339 | |||||||
chr6:39812390 | T | C | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+19925T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812390 | |||||||
chr6:39812472 | G | A | 22 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0213 others(19): Show |
23 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+20007G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812472 | |||||||
chr6:39812551 | T | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
27 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+20086T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812551 | |||||||
chr6:39812586 | C | T | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-57+20121C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812586 | |||||||
chr6:39812617 | ATTC | A | 42 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(39): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+20155_-57+2015 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812617 | ||||||
chr6:39812646 | G | GTGGAGTC others(13): Show |
39 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(36): Show |
39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-57+20189_-57+2019 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812646 | ||||||
chr6:39812646 | G | GTGGAGTC others(13): Show |
3 | a0001c0001t0001g0165 a0001c0005t0011g0125 a0001c0045t0002g0164 |
3 | HG02280.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+20188_-57+2020 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39812646 | ||||||
chr6:39812663 | C | G | 39 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(36): Show |
39 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-57+20198C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812663 | |||||||
chr6:39812925 | A | G | 1 | a0002c0010t0002g0256 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-57+20460A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812925 | |||||||
chr6:39812928 | A | G | 83 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(80): Show |
83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+20463A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39812928 | |||||||
chr6:39813146 | TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0002g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-57+20688_-57+2070 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39813146 | ||||||
chr6:39813166 | G | A | 4 | a0001c0001t0001g0220 a0001c0001t0008g0215 a0001c0001t0008g0218 others(1): Show |
4 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+20701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813166 | |||||||
chr6:39813167 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+20702C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813167 | |||||||
chr6:39813169 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+20704T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813169 | |||||||
chr6:39813215 | A | T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-57+20750A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813215 | |||||||
chr6:39813537 | C | A | 42 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(39): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+21072C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813537 | |||||||
chr6:39813550 | T | C | 2 | a0001c0001t0001g0233 a0007c0023t0007g0232 |
2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+21085T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813550 | |||||||
chr6:39813565 | T | A | 42 | a0001c0001t0001g0025 a0001c0001t0001g0124 a0001c0001t0001g0127 others(39): Show |
42 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+21100T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813565 | |||||||
chr6:39813578 | CT | C | 14 | a0001c0001t0001g0234 a0001c0001t0001g0271 a0001c0001t0010g0268 others(11): Show |
14 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+21114delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813578 | |||||||
chr6:39813580 | C | G | 1 | a0001c0007t0013g0245 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-57+21115C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813580 | |||||||
chr6:39813708 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-57+21243C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813708 | |||||||
chr6:39813728 | C | T | 5 | a0001c0003t0016g0283 a0001c0006t0020g0284 a0001c0008t0005g0167 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+21263C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813728 | |||||||
chr6:39813784 | G | A | 120 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(117): Show |
120 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-57+21319G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39813784 | |||||||
chr6:39814016 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+21551C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814016 | |||||||
chr6:39814058 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
28 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-57+21593C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814058 | |||||||
chr6:39814083 | C | G | 1 | a0001c0002t0002g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-57+21618C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814083 | |||||||
chr6:39814188 | C | CT | 8 | a0001c0001t0001g0113 a0001c0001t0001g0209 a0001c0005t0011g0043 others(5): Show |
8 | HG01255.hp2 HG01361.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+21736dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39814188 | ||||||
chr6:39814188 | CT | C | 89 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(86): Show |
89 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.-57+21736delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39814188 | ||||||
chr6:39814191 | T | TC | 92 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(89): Show |
92 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-57+21726_-57+2172 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814191 | |||||||
chr6:39814316 | C | T | 190 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(187): Show |
190 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+21851C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814316 | |||||||
chr6:39814455 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+21990G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814455 | |||||||
chr6:39814461 | G | A | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+21996G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814461 | |||||||
chr6:39814503 | T | G | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+22038T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814503 | |||||||
chr6:39814580 | A | G | 4 | a0001c0005t0011g0043 a0001c0033t0001g0045 a0001c0046t0001g0044 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22115A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814580 | |||||||
chr6:39814827 | C | G | 2 | a0001c0003t0016g0207 a0005c0029t0001g0178 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-57+22362C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814827 | |||||||
chr6:39814830 | C | G | 4 | a0001c0005t0011g0043 a0001c0033t0001g0045 a0001c0046t0001g0044 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22365C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39814830 | |||||||
chr6:39815083 | A | C | 1 | a0001c0003t0003g0179 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-57+22618A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815083 | |||||||
chr6:39815166 | G | T | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-57+22701G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815166 | |||||||
chr6:39815372 | A | G | 1 | a0006c0040t0002g0229 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-57+22907A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815372 | |||||||
chr6:39815393 | C | T | 4 | a0001c0005t0011g0043 a0001c0033t0001g0045 a0001c0046t0001g0044 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+22928C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815393 | |||||||
chr6:39815439 | C | A | 2 | a0001c0004t0003g0116 a0001c0006t0001g0294 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-57+22974C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815439 | |||||||
chr6:39815468 | C | A | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23003C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815468 | |||||||
chr6:39815498 | C | T | 1 | a0002c0015t0003g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-57+23033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815498 | |||||||
chr6:39815542 | A | G | 156 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(153): Show |
156 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.-57+23077A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815542 | |||||||
chr6:39815582 | G | T | 204 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(201): Show |
204 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.-57+23117G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815582 | |||||||
chr6:39815594 | A | G | 9 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0202 others(6): Show |
9 | HG00423.hp2 HG00609.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+23129A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815594 | |||||||
chr6:39815620 | C | T | 1 | a0001c0003t0003g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-57+23155C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815620 | |||||||
chr6:39815651 | T | TAC | 30 | a0001c0001t0001g0184 a0001c0001t0001g0186 a0001c0001t0001g0205 others(27): Show |
30 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+23219_-57+2322 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACAC | 34 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0202 others(31): Show |
34 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+23217_-57+2322 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACAC | 14 | a0001c0001t0001g0035 a0001c0001t0001g0152 a0001c0001t0001g0234 others(11): Show |
14 | HG00642.hp2 HG02083.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.-57+23215_-57+2322 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACACA others(1): Show |
12 | a0001c0001t0001g0113 a0001c0001t0001g0131 a0001c0001t0025g0032 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+23213_-57+2322 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0183 a0001c0002t0002g0021 a0001c0002t0002g0024 others(4): Show |
7 | HG02056.hp2 HG02135.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+23211_-57+2322 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACACA others(5): Show |
2 | a0001c0003t0003g0269 a0011c0043t0005g0151 |
2 | HG03225.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-57+23209_-57+2322 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACACA others(7): Show |
1 | a0001c0002t0002g0020 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-57+23207_-57+2322 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | T | TACACACA others(19): Show |
1 | a0001c0002t0002g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+23195_-57+2322 others(30): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TAC | T | 20 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0213 others(17): Show |
21 | HG00741.hp1 HG01257.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57+23219_-57+2322 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TACACAC | T | 11 | a0001c0001t0001g0110 a0001c0001t0001g0165 a0001c0002t0002g0108 others(8): Show |
11 | HG00741.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23215_-57+2322 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TACACACA others(1): Show |
T | 144 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(141): Show |
144 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-57+23213_-57+2322 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TACACACA others(3): Show |
T | 6 | a0001c0003t0016g0283 a0001c0004t0006g0090 a0001c0006t0020g0284 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+23211_-57+2322 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TACACACA others(5): Show |
T | 1 | a0001c0006t0001g0015 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-57+23209_-57+2322 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815651 | TACACACA others(9): Show |
T | 4 | a0001c0005t0011g0043 a0001c0033t0001g0045 a0001c0046t0001g0044 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+23205_-57+2322 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39815651 | ||||||
chr6:39815711 | G | A | 2 | a0001c0001t0001g0233 a0007c0023t0007g0232 |
2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+23246G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815711 | |||||||
chr6:39815754 | T | C | 1 | a0001c0003t0003g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-57+23289T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815754 | |||||||
chr6:39815853 | A | C | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23388A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815853 | |||||||
chr6:39815993 | C | T | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23528C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39815993 | |||||||
chr6:39816056 | C | T | 2 | a0001c0001t0001g0165 a0001c0045t0002g0164 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-57+23591C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816056 | |||||||
chr6:39816106 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-57+23641G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816106 | |||||||
chr6:39816204 | C | T | 11 | a0001c0001t0001g0234 a0001c0001t0001g0271 a0001c0001t0010g0268 others(8): Show |
11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23739C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816204 | |||||||
chr6:39816358 | T | C | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+23893T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816358 | |||||||
chr6:39816379 | A | G | 2 | a0001c0005t0003g0291 a0001c0005t0014g0176 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+23914A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816379 | |||||||
chr6:39816413 | G | T | 11 | a0001c0001t0001g0234 a0001c0001t0001g0271 a0001c0001t0010g0268 others(8): Show |
11 | HG02083.hp1 HG02135.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+23948G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816413 | |||||||
chr6:39816455 | G | A | 1 | a0014c0021t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57+23990G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816455 | |||||||
chr6:39816573 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+24108T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816573 | |||||||
chr6:39816589 | C | A | 180 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(177): Show |
180 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-57+24124C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816589 | |||||||
chr6:39816775 | T | C | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+24310T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816775 | |||||||
chr6:39816831 | T | A | 1 | a0001c0002t0002g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-57+24366T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816831 | |||||||
chr6:39816840 | G | A | 159 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(156): Show |
159 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.-57+24375G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816840 | |||||||
chr6:39816857 | C | T | 8 | a0001c0009t0009g0163 a0001c0013t0023g0170 a0001c0013t0023g0171 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+24392C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816857 | |||||||
chr6:39816858 | G | A | 2 | a0001c0008t0005g0167 a0001c0036t0022g0168 |
2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-57+24393G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816858 | |||||||
chr6:39816927 | A | G | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
27 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+24462A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816927 | |||||||
chr6:39816944 | G | A | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(159): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+24479G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39816944 | |||||||
chr6:39817422 | G | A | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-57+24957G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817422 | |||||||
chr6:39817595 | G | A | 2 | a0001c0005t0003g0291 a0001c0005t0014g0176 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-57+25130G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817595 | |||||||
chr6:39817760 | T | C | 1 | a0001c0001t0017g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-57+25295T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817760 | |||||||
chr6:39817783 | C | G | 2 | a0001c0001t0001g0113 a0009c0019t0003g0037 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-57+25318C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817783 | |||||||
chr6:39817835 | C | A | 1 | a0001c0006t0001g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+25370C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817835 | |||||||
chr6:39817905 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+25440A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817905 | |||||||
chr6:39817944 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+25479C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39817944 | |||||||
chr6:39818051 | C | T | 1 | a0001c0004t0031g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+25586C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818051 | |||||||
chr6:39818093 | C | T | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+25628C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818093 | |||||||
chr6:39818127 | C | T | 76 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0183 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-57+25662C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818127 | |||||||
chr6:39818136 | G | A | 12 | a0001c0002t0030g0175 a0001c0003t0003g0117 a0001c0004t0021g0101 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+25671G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818136 | |||||||
chr6:39818137 | T | C | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
178 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-57+25672T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818137 | |||||||
chr6:39818138 | C | A | 3 | a0001c0001t0001g0068 a0001c0003t0039g0091 a0010c0047t0001g0067 |
3 | HG02683.hp1 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-57+25673C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818138 | |||||||
chr6:39818182 | T | TA | 43 | a0001c0001t0001g0124 a0001c0001t0001g0186 a0001c0001t0001g0209 others(40): Show |
43 | HG00621.hp1 HG01175.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.-57+25741dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | ||||||
chr6:39818182 | T | TAA | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
27 | HG00621.hp2 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57+25740_-57+2574 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | ||||||
chr6:39818182 | TA | T | 11 | a0001c0001t0001g0162 a0001c0001t0001g0184 a0001c0001t0001g0200 others(8): Show |
11 | HG01169.hp2 HG01515.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+25741delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | ||||||
chr6:39818182 | TAAAAAAA | T | 7 | a0001c0003t0016g0283 a0001c0006t0020g0284 a0001c0008t0005g0285 others(4): Show |
7 | HG02055.hp2 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+25735_-57+2574 others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39818182 | ||||||
chr6:39818200 | A | AC | 13 | a0001c0002t0030g0175 a0001c0003t0003g0117 a0001c0004t0021g0101 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+25735_-57+2573 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818200 | |||||||
chr6:39818204 | A | AC | 85 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(82): Show |
86 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-57+25739_-57+2574 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818204 | |||||||
chr6:39818204 | A | C | 1 | a0001c0002t0002g0039 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-57+25739A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818204 | |||||||
chr6:39818303 | C | T | 3 | a0001c0002t0002g0275 a0001c0006t0001g0033 a0001c0012t0002g0297 |
3 | HG02486.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-57+25838C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818303 | |||||||
chr6:39818317 | A | G | 99 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0066 others(96): Show |
100 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-57+25852A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818317 | |||||||
chr6:39818351 | C | A | 165 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(162): Show |
166 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-57+25886C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818351 | |||||||
chr6:39818539 | G | A | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+26074G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818539 | |||||||
chr6:39818582 | C | A | 13 | a0001c0001t0001g0119 a0001c0001t0001g0186 a0001c0001t0001g0200 others(10): Show |
13 | HG00423.hp2 HG00621.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+26117C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818582 | |||||||
chr6:39818643 | G | A | 2 | a0001c0001t0001g0233 a0007c0023t0007g0232 |
2 | HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-57+26178G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818643 | |||||||
chr6:39818867 | T | C | 218 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(215): Show |
219 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.-57+26402T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39818867 | |||||||
chr6:39819012 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-57+26547G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819012 | |||||||
chr6:39819088 | T | C | 250 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.-57+26623T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819088 | |||||||
chr6:39819091 | C | T | 2 | a0001c0001t0001g0119 a0001c0004t0003g0103 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-57+26626C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819091 | |||||||
chr6:39819242 | G | A | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-57+26777G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819242 | |||||||
chr6:39819273 | G | T | 7 | a0001c0001t0001g0165 a0001c0001t0001g0226 a0001c0001t0001g0272 others(4): Show |
7 | HG02738.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-57+26808G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819273 | |||||||
chr6:39819301 | G | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+26836G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819301 | |||||||
chr6:39819302 | A | G | 5 | a0001c0005t0011g0125 a0001c0005t0014g0176 a0001c0009t0009g0112 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+26837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819302 | |||||||
chr6:39819408 | A | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0119 a0001c0001t0001g0280 others(3): Show |
6 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+26943A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819408 | |||||||
chr6:39819529 | G | A | 1 | a0001c0006t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-57+27064G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819529 | |||||||
chr6:39819581 | G | GA | 9 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0003t0003g0069 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+27123dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39819581 | ||||||
chr6:39819760 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+27295T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819760 | |||||||
chr6:39819771 | G | A | 13 | a0001c0001t0001g0124 a0001c0001t0019g0051 a0001c0002t0002g0180 others(10): Show |
13 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+27306G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819771 | |||||||
chr6:39819836 | T | C | 13 | a0001c0001t0001g0124 a0001c0001t0019g0051 a0001c0002t0002g0180 others(10): Show |
13 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-57+27371T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819836 | |||||||
chr6:39819856 | G | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+27391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819856 | |||||||
chr6:39819865 | A | T | 3 | a0001c0002t0002g0133 a0001c0005t0011g0031 a0001c0009t0009g0128 |
3 | HG01109.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+27400A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819865 | |||||||
chr6:39819903 | C | T | 75 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(72): Show |
75 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-57+27438C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819903 | |||||||
chr6:39819960 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-57+27495C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819960 | |||||||
chr6:39819983 | C | T | 16 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0002t0002g0275 others(13): Show |
16 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+27518C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39819983 | |||||||
chr6:39820003 | A | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(16): Show |
19 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-57+27538A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820003 | |||||||
chr6:39820049 | G | T | 2 | a0001c0002t0002g0185 a0001c0003t0003g0267 |
2 | HG02135.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-57+27584G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820049 | |||||||
chr6:39820112 | T | C | 109 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(106): Show |
109 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-57+27647T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820112 | |||||||
chr6:39820231 | C | T | 1 | a0002c0010t0002g0255 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-57+27766C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820231 | |||||||
chr6:39820405 | C | T | 1 | a0001c0009t0009g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-57+27940C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820405 | |||||||
chr6:39820522 | C | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0003t0007g0016 |
3 | HG01175.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-57+28057C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820522 | |||||||
chr6:39820582 | G | T | 98 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-57+28117G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820582 | |||||||
chr6:39820626 | A | C | 9 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0003t0003g0069 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+28161A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820626 | |||||||
chr6:39820720 | A | G | 108 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(105): Show |
109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-57+28255A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820720 | |||||||
chr6:39820753 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-57+28288A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820753 | |||||||
chr6:39820825 | G | A | 9 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0003t0003g0069 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+28360G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820825 | |||||||
chr6:39820875 | G | A | 1 | a0001c0003t0016g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+28410G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820875 | |||||||
chr6:39820972 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01891.hp2 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-57+28507G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39820972 | |||||||
chr6:39821121 | C | A | 2 | a0001c0004t0003g0116 a0009c0019t0003g0037 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-57+28656C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821121 | |||||||
chr6:39821175 | GAGCCAC | G | 18 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0002t0002g0275 others(15): Show |
18 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+28712_-57+2871 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39821175 | ||||||
chr6:39821184 | ATT | A | 18 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0002t0002g0275 others(15): Show |
18 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+28720_-57+2872 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821184 | |||||||
chr6:39821220 | G | C | 3 | a0001c0001t0001g0202 a0001c0002t0002g0203 a0001c0007t0013g0065 |
3 | NA18956.hp1 NA18993.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-57+28755G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821220 | |||||||
chr6:39821268 | A | G | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+28803A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821268 | |||||||
chr6:39821290 | G | A | 3 | a0001c0002t0002g0009 a0001c0002t0002g0237 a0001c0002t0002g0295 |
3 | NA18973.hp2 NA18982.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-57+28825G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821290 | |||||||
chr6:39821421 | G | A | 1 | a0002c0010t0002g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57+28956G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821421 | |||||||
chr6:39821620 | G | T | 3 | a0001c0004t0021g0101 a0001c0004t0035g0126 a0001c0008t0005g0102 |
3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+29155G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821620 | |||||||
chr6:39821794 | C | G | 1 | a0001c0004t0006g0075 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-57+29329C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821794 | |||||||
chr6:39821815 | A | C | 48 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-57+29350A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821815 | |||||||
chr6:39821955 | G | A | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-57+29490G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39821955 | |||||||
chr6:39822085 | G | C | 1 | a0001c0004t0004g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-57+29620G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822085 | |||||||
chr6:39822219 | A | G | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+29754A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822219 | |||||||
chr6:39822267 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0220 a0001c0002t0002g0022 |
3 | HG01261.hp2 HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-57+29802C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822267 | |||||||
chr6:39822411 | C | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0280 others(10): Show |
13 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57+29946C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822411 | |||||||
chr6:39822430 | T | C | 12 | a0001c0002t0002g0039 a0001c0002t0002g0277 a0001c0004t0031g0293 others(9): Show |
12 | HG02280.hp1 HG02451.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+29965T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822430 | |||||||
chr6:39822434 | G | A | 1 | a0001c0006t0001g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-57+29969G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822434 | |||||||
chr6:39822483 | G | T | 1 | a0001c0002t0002g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+30018G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822483 | |||||||
chr6:39822527 | A | C | 77 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(74): Show |
77 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-57+30062A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822527 | |||||||
chr6:39822998 | T | C | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+30533T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39822998 | |||||||
chr6:39823164 | C | T | 97 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-57+30699C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823164 | |||||||
chr6:39823269 | T | C | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+30804T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823269 | |||||||
chr6:39823307 | C | A | 8 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(5): Show |
8 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+30842C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823307 | |||||||
chr6:39823519 | C | G | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-57+31054C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823519 | |||||||
chr6:39823568 | G | C | 2 | a0001c0044t0022g0115 a0008c0038t0009g0042 |
2 | HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-57+31103G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823568 | |||||||
chr6:39823574 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0019g0051 a0001c0002t0002g0180 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+31109C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823574 | |||||||
chr6:39823718 | C | G | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+31253C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823718 | |||||||
chr6:39823781 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0019g0051 a0001c0002t0002g0180 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+31316G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823781 | |||||||
chr6:39823810 | C | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0161 a0001c0001t0001g0258 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+31345C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823810 | |||||||
chr6:39823883 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0008g0150 |
2 | HG01081.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-57+31418C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823883 | |||||||
chr6:39823916 | T | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-57+31451T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823916 | |||||||
chr6:39823988 | C | T | 97 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-57+31523C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39823988 | |||||||
chr6:39824119 | G | A | 1 | a0013c0034t0001g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-57+31654G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824119 | |||||||
chr6:39824165 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+31700G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824165 | |||||||
chr6:39824299 | A | G | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+31834A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824299 | |||||||
chr6:39824308 | C | A | 3 | a0001c0001t0001g0119 a0001c0005t0011g0031 a0001c0009t0009g0128 |
3 | HG02970.hp2 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-57+31843C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824308 | |||||||
chr6:39824476 | G | A | 6 | a0001c0002t0002g0275 a0001c0004t0003g0116 a0001c0006t0028g0188 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-31771G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824476 | |||||||
chr6:39824503 | T | A | 108 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(105): Show |
108 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-56-31744T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824503 | |||||||
chr6:39824605 | A | C | 1 | a0001c0002t0002g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-56-31642A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824605 | |||||||
chr6:39824737 | T | C | 98 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-56-31510T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824737 | |||||||
chr6:39824755 | G | A | 6 | a0001c0002t0002g0275 a0001c0004t0003g0116 a0001c0006t0028g0188 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-31492G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824755 | |||||||
chr6:39824769 | G | A | 9 | a0001c0001t0001g0072 a0001c0001t0001g0161 a0001c0001t0001g0258 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-31478G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824769 | |||||||
chr6:39824981 | G | A | 1 | a0001c0001t0017g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-56-31266G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39824981 | |||||||
chr6:39825087 | A | G | 25 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(22): Show |
25 | HG00099.hp2 HG00642.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-56-31160A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825087 | |||||||
chr6:39825112 | G | A | 9 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0003t0003g0177 others(6): Show |
9 | HG01081.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-31135G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825112 | |||||||
chr6:39825156 | A | C | 117 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(114): Show |
118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-31091A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825156 | |||||||
chr6:39825196 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-31051C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825196 | |||||||
chr6:39825262 | C | T | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-30985C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825262 | |||||||
chr6:39825270 | G | T | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-30977G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825270 | |||||||
chr6:39825272 | T | C | 12 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0280 others(9): Show |
12 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-30975T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825272 | |||||||
chr6:39825384 | T | TAAAAC | 17 | a0001c0001t0001g0035 a0001c0001t0017g0266 a0001c0001t0019g0122 others(14): Show |
17 | HG01978.hp1 HG02280.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-30821_-56-3081 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825384 | T | TAAAACAA others(3): Show |
2 | a0001c0003t0016g0123 a0003c0024t0001g0029 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-56-30826_-56-3081 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825384 | TAAAAC | T | 106 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(103): Show |
107 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-56-30821_-56-3081 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825384 | TAAAACAA others(3): Show |
T | 8 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0010g0268 others(5): Show |
8 | HG01361.hp2 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-30826_-56-3081 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825384 | TAAAACAA others(8): Show |
T | 12 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 others(9): Show |
12 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-30831_-56-3081 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825384 | TAAAACAA others(13): Show |
T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-30836_-56-3081 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825384 | ||||||
chr6:39825443 | GT | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0019g0051 others(17): Show |
20 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-56-30802delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39825443 | ||||||
chr6:39825444 | T | TG | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0086 others(38): Show |
41 | HG00609.hp1 HG00741.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-56-30803_-56-3080 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825444 | |||||||
chr6:39825444 | T | TGGG | 3 | a0001c0001t0001g0124 a0001c0004t0021g0061 a0001c0009t0009g0163 |
3 | HG02055.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-30803_-56-3080 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825444 | |||||||
chr6:39825445 | T | G | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-56-30802T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825445 | |||||||
chr6:39825447 | GT | G | 9 | a0001c0002t0002g0277 a0001c0004t0031g0293 a0001c0005t0011g0043 others(6): Show |
9 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-30799delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825447 | |||||||
chr6:39825448 | T | G | 244 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-56-30799T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825448 | |||||||
chr6:39825452 | G | T | 4 | a0001c0001t0001g0113 a0001c0003t0016g0207 a0001c0036t0022g0168 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-30795G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825452 | |||||||
chr6:39825453 | G | T | 3 | a0001c0003t0016g0207 a0001c0036t0022g0168 a0005c0029t0001g0178 |
3 | HG02818.hp2 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-56-30794G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825453 | |||||||
chr6:39825455 | C | G | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(44): Show |
48 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-56-30792C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825455 | |||||||
chr6:39825534 | G | A | 50 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-56-30713G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825534 | |||||||
chr6:39825552 | C | T | 5 | a0001c0001t0001g0124 a0001c0003t0003g0117 a0001c0004t0021g0061 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-30695C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825552 | |||||||
chr6:39825557 | C | A | 3 | a0001c0001t0025g0032 a0001c0022t0020g0048 a0011c0043t0005g0151 |
3 | HG03225.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-56-30690C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825557 | |||||||
chr6:39825670 | G | C | 9 | a0001c0001t0001g0035 a0001c0002t0002g0114 a0001c0002t0002g0192 others(6): Show |
9 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-30577G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825670 | |||||||
chr6:39825704 | T | C | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(73): Show |
76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-30543T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825704 | |||||||
chr6:39825754 | G | C | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-30493G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825754 | |||||||
chr6:39825948 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-56-30299A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39825948 | |||||||
chr6:39826155 | C | T | 4 | a0001c0003t0003g0286 a0001c0003t0003g0288 a0001c0003t0003g0289 others(1): Show |
4 | HG02083.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-30092C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826155 | |||||||
chr6:39826264 | A | AT | 92 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0076 others(89): Show |
92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-56-29973dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39826264 | ||||||
chr6:39826483 | C | G | 1 | a0001c0002t0002g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-56-29764C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826483 | |||||||
chr6:39826582 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0019g0051 a0001c0002t0002g0180 others(5): Show |
8 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-29665C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826582 | |||||||
chr6:39826877 | A | G | 107 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(104): Show |
107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-56-29370A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39826877 | |||||||
chr6:39827030 | C | G | 116 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(113): Show |
117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-56-29217C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827030 | |||||||
chr6:39827142 | G | A | 1 | a0001c0006t0020g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-56-29105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827142 | |||||||
chr6:39827238 | C | T | 1 | a0001c0003t0003g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-56-29009C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827238 | |||||||
chr6:39827263 | G | GC | 107 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(104): Show |
107 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-56-28984_-56-2898 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827263 | |||||||
chr6:39827313 | G | A | 7 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-28934G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827313 | |||||||
chr6:39827345 | G | A | 11 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0280 others(8): Show |
11 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-28902G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827345 | |||||||
chr6:39827424 | A | G | 16 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(13): Show |
16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28823A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827424 | |||||||
chr6:39827455 | G | A | 7 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-28792G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827455 | |||||||
chr6:39827469 | T | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(13): Show |
16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28778T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827469 | |||||||
chr6:39827513 | C | T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(13): Show |
16 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-28734C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827513 | |||||||
chr6:39827558 | G | A | 1 | a0001c0004t0004g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-56-28689G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827558 | |||||||
chr6:39827564 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0220 a0001c0002t0002g0022 |
3 | HG01261.hp2 HG01515.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-56-28683G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827564 | |||||||
chr6:39827577 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-28670C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827577 | |||||||
chr6:39827652 | T | C | 18 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(15): Show |
18 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-56-28595T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827652 | |||||||
chr6:39827773 | C | T | 80 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(77): Show |
80 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-56-28474C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827773 | |||||||
chr6:39827774 | A | G | 256 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(253): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.-56-28473A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827774 | |||||||
chr6:39827829 | G | C | 97 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(94): Show |
97 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-56-28418G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827829 | |||||||
chr6:39827844 | T | TCTC | 127 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(124): Show |
127 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-56-28401_-56-2840 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39827844 | ||||||
chr6:39827938 | C | T | 1 | a0001c0002t0002g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-56-28309C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39827938 | |||||||
chr6:39828017 | G | A | 28 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(25): Show |
28 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-56-28230G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828017 | |||||||
chr6:39828112 | G | A | 1 | a0001c0006t0001g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-28135G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828112 | |||||||
chr6:39828221 | C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-28026C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828221 | |||||||
chr6:39828226 | A | G | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(73): Show |
76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-28021A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828226 | |||||||
chr6:39828556 | C | T | 7 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-27691C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828556 | |||||||
chr6:39828559 | C | G | 96 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-27688C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828559 | |||||||
chr6:39828567 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0003t0003g0117 |
3 | HG03098.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-56-27680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828567 | |||||||
chr6:39828570 | C | CTTTTTTT others(3): Show |
30 | a0001c0001t0001g0127 a0001c0001t0001g0137 a0001c0001t0001g0138 others(27): Show |
30 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-56-27675_-56-2766 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | ||||||
chr6:39828570 | C | CTTTTTTT others(4): Show |
19 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(16): Show |
19 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-56-27676_-56-2766 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | ||||||
chr6:39828570 | C | CTTTTTTT others(5): Show |
35 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0110 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | ||||||
chr6:39828570 | C | CTTTTTTT others(6): Show |
7 | a0001c0001t0001g0280 a0001c0002t0002g0185 a0001c0002t0002g0203 others(4): Show |
7 | HG02055.hp1 HG03927.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(17): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | ||||||
chr6:39828570 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0124 a0001c0001t0001g0281 |
3 | HG01891.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-27666_-56-2766 others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39828570 | ||||||
chr6:39828587 | G | A | 5 | a0001c0001t0019g0051 a0001c0006t0001g0159 a0001c0008t0005g0167 others(2): Show |
5 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-27660G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828587 | |||||||
chr6:39828665 | T | C | 9 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-27582T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828665 | |||||||
chr6:39828688 | G | A | 89 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(86): Show |
89 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-56-27559G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828688 | |||||||
chr6:39828710 | G | A | 4 | a0001c0003t0003g0003 a0001c0003t0003g0036 a0001c0003t0003g0252 others(1): Show |
4 | HG01943.hp2 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-27537G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828710 | |||||||
chr6:39828723 | C | T | 7 | a0001c0001t0019g0051 a0001c0002t0002g0180 a0001c0004t0004g0172 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-27524C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828723 | |||||||
chr6:39828724 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0019g0122 a0001c0003t0007g0002 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-27523G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828724 | |||||||
chr6:39828768 | G | T | 79 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(76): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-56-27479G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828768 | |||||||
chr6:39828808 | G | A | 2 | a0001c0001t0001g0156 a0001c0002t0002g0121 |
2 | HG01261.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-56-27439G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828808 | |||||||
chr6:39828891 | C | T | 28 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(25): Show |
28 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-56-27356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828891 | |||||||
chr6:39828895 | C | T | 17 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0124 others(14): Show |
17 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-56-27352C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828895 | |||||||
chr6:39828896 | C | G | 2 | a0001c0004t0021g0061 a0001c0009t0009g0163 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-27351C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828896 | |||||||
chr6:39828908 | G | A | 136 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(133): Show |
136 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-56-27339G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828908 | |||||||
chr6:39828933 | T | C | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-27314T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39828933 | |||||||
chr6:39829064 | C | G | 9 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0003t0003g0177 others(6): Show |
9 | HG01081.hp1 HG01255.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-27183C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829064 | |||||||
chr6:39829134 | C | T | 48 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-56-27113C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829134 | |||||||
chr6:39829167 | C | T | 26 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(23): Show |
26 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.-56-27080C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829167 | |||||||
chr6:39829176 | T | C | 96 | a0001c0001t0001g0040 a0001c0001t0001g0076 a0001c0001t0001g0077 others(93): Show |
96 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-27071T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829176 | |||||||
chr6:39829374 | C | T | 1 | a0001c0002t0002g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-56-26873C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829374 | |||||||
chr6:39829420 | C | T | 2 | a0001c0003t0003g0289 a0005c0028t0004g0290 |
2 | NA18747.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-56-26827C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829420 | |||||||
chr6:39829503 | G | C | 1 | a0001c0031t0040g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-56-26744G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829503 | |||||||
chr6:39829608 | T | C | 76 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(73): Show |
76 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-56-26639T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39829608 | |||||||
chr6:39830076 | G | T | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-56-26171G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830076 | |||||||
chr6:39830181 | C | T | 10 | a0001c0001t0001g0161 a0001c0001t0001g0258 a0001c0001t0019g0122 others(7): Show |
10 | HG01074.hp1 HG01109.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-26066C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830181 | |||||||
chr6:39830396 | C | T | 19 | a0001c0001t0001g0209 a0001c0001t0025g0032 a0001c0002t0002g0275 others(16): Show |
19 | HG01081.hp1 HG01255.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-56-25851C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830396 | |||||||
chr6:39830463 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-25784C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830463 | |||||||
chr6:39830485 | G | A | 1 | a0002c0015t0003g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-56-25762G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830485 | |||||||
chr6:39830505 | G | C | 1 | a0001c0006t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-56-25742G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830505 | |||||||
chr6:39830547 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-25700C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830547 | |||||||
chr6:39830549 | G | A | 10 | a0001c0001t0001g0119 a0001c0002t0002g0277 a0001c0004t0031g0293 others(7): Show |
10 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-25698G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830549 | |||||||
chr6:39830581 | A | C | 106 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(103): Show |
106 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-56-25666A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830581 | |||||||
chr6:39830668 | C | T | 1 | a0001c0004t0006g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-56-25579C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830668 | |||||||
chr6:39830669 | G | A | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-25578G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830669 | |||||||
chr6:39830690 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-56-25557C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830690 | |||||||
chr6:39830695 | A | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0003t0003g0117 others(3): Show |
6 | HG02055.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-25552A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830695 | |||||||
chr6:39830702 | A | G | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-25545A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830702 | |||||||
chr6:39830784 | T | C | 2 | a0001c0006t0001g0041 a0001c0008t0005g0026 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-56-25463T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830784 | |||||||
chr6:39830892 | C | T | 1 | a0001c0003t0016g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-25355C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830892 | |||||||
chr6:39830933 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0272 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-56-25314C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830933 | |||||||
chr6:39830935 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-56-25312A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830935 | |||||||
chr6:39830986 | A | G | 2 | a0001c0001t0001g0124 a0001c0003t0003g0117 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-25261A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39830986 | |||||||
chr6:39831083 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-56-25164A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831083 | |||||||
chr6:39831137 | G | T | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-25110G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831137 | |||||||
chr6:39831240 | G | A | 2 | a0001c0002t0002g0020 a0001c0002t0002g0021 |
2 | NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-25007G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831240 | |||||||
chr6:39831364 | C | T | 2 | a0001c0004t0021g0061 a0001c0009t0009g0163 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-24883C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831364 | |||||||
chr6:39831416 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-24831T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831416 | |||||||
chr6:39831551 | TCTAGGAT others(5): Show |
T | 1 | a0001c0001t0001g0258 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-56-24694_-56-2468 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831551 | ||||||
chr6:39831696 | TG | T | 79 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(76): Show |
80 | HG00323.hp1 HG00423.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-56-24545delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831696 | ||||||
chr6:39831697 | G | T | 3 | a0001c0001t0001g0137 a0001c0002t0002g0254 a0001c0003t0003g0036 |
3 | HG01257.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-56-24550G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831697 | |||||||
chr6:39831735 | C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-24512C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831735 | |||||||
chr6:39831738 | G | A | 2 | a0001c0001t0001g0261 a0001c0002t0002g0260 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-56-24509G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831738 | |||||||
chr6:39831780 | A | AGGGGGCA others(9): Show |
1 | a0001c0004t0021g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-56-24461_-56-2444 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831780 | ||||||
chr6:39831792 | C | T | 2 | a0001c0001t0001g0124 a0001c0008t0005g0102 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-56-24455C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831792 | |||||||
chr6:39831796 | G | GGGGGGCA others(93): Show |
1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-24446_-56-2444 others(104): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831796 | ||||||
chr6:39831798 | G | GGGGCAGG others(8): Show |
98 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(95): Show |
98 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-56-24446_-56-2444 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831798 | ||||||
chr6:39831834 | G | GGGGTAGG others(111): Show |
1 | a0001c0001t0001g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-24356_-56-2435 others(122): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831834 | ||||||
chr6:39831892 | G | A | 49 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0088 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-56-24355G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831892 | |||||||
chr6:39831892 | G | GTGCACTG others(111): Show |
1 | a0001c0004t0026g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-56-24331_-56-2433 others(122): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39831892 | ||||||
chr6:39831928 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-56-24319C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831928 | |||||||
chr6:39831938 | G | GA | 99 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0072 others(96): Show |
99 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-56-24309_-56-2430 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39831938 | |||||||
chr6:39832053 | G | A | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-24194G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832053 | |||||||
chr6:39832113 | C | T | 1 | a0001c0003t0003g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-56-24134C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832113 | |||||||
chr6:39832197 | A | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0264 a0001c0002t0002g0263 others(1): Show |
4 | HG00735.hp2 HG01952.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24050A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832197 | |||||||
chr6:39832238 | A | G | 84 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(81): Show |
84 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-56-24009A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832238 | |||||||
chr6:39832399 | C | T | 52 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(49): Show |
52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23848C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832399 | |||||||
chr6:39832436 | AT | A | 52 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(49): Show |
52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23809delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832436 | ||||||
chr6:39832489 | C | T | 1 | a0001c0002t0002g0295 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-56-23758C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832489 | |||||||
chr6:39832584 | T | C | 52 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(49): Show |
52 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-23663T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832584 | |||||||
chr6:39832591 | GTC | G | 51 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0086 others(48): Show |
51 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-56-23652_-56-2365 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832591 | ||||||
chr6:39832606 | G | A | 1 | a0001c0008t0005g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-23641G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832606 | |||||||
chr6:39832662 | G | C | 1 | a0001c0006t0001g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-56-23585G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832662 | |||||||
chr6:39832693 | CTTCCTGG others(15): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-56-23546_-56-2352 others(26): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39832693 | ||||||
chr6:39832762 | T | A | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23485T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832762 | |||||||
chr6:39832770 | G | A | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-23477G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832770 | |||||||
chr6:39832801 | G | A | 37 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(34): Show |
37 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.-56-23446G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832801 | |||||||
chr6:39832835 | C | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23412C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832835 | |||||||
chr6:39832846 | C | T | 10 | a0001c0001t0001g0035 a0001c0002t0002g0114 a0001c0002t0002g0192 others(7): Show |
10 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-23401C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832846 | |||||||
chr6:39832854 | T | C | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23393T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832854 | |||||||
chr6:39832881 | C | A | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-23366C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832881 | |||||||
chr6:39832893 | T | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-23354T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832893 | |||||||
chr6:39832934 | C | G | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-23313C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832934 | |||||||
chr6:39832996 | G | A | 7 | a0001c0001t0001g0204 a0001c0001t0001g0247 a0001c0002t0002g0187 others(4): Show |
7 | HG00621.hp2 NA18747.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-23251G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39832996 | |||||||
chr6:39833052 | G | A | 1 | a0001c0007t0012g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-23195G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833052 | |||||||
chr6:39833061 | C | T | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-23186C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833061 | |||||||
chr6:39833198 | G | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(32): Show |
35 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-56-23049G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833198 | |||||||
chr6:39833270 | C | G | 7 | a0001c0001t0001g0113 a0001c0002t0002g0133 a0001c0004t0021g0101 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-22977C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833270 | |||||||
chr6:39833458 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-22789C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833458 | |||||||
chr6:39833527 | C | T | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-22720C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833527 | |||||||
chr6:39833561 | G | C | 3 | a0001c0004t0021g0101 a0001c0004t0035g0126 a0001c0008t0005g0102 |
3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-22686G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833561 | |||||||
chr6:39833725 | A | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22522A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833725 | |||||||
chr6:39833839 | A | G | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-22408A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833839 | |||||||
chr6:39833944 | A | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22303A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39833944 | |||||||
chr6:39834083 | G | A | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-22164G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834083 | |||||||
chr6:39834428 | G | C | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-21819G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834428 | |||||||
chr6:39834428 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-56-21819G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834428 | |||||||
chr6:39834459 | G | A | 3 | a0001c0004t0021g0101 a0001c0004t0035g0126 a0001c0008t0005g0102 |
3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-21788G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834459 | |||||||
chr6:39834548 | G | A | 1 | a0001c0006t0001g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-21699G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834548 | |||||||
chr6:39834813 | C | A | 65 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(62): Show |
65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-56-21434C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834813 | |||||||
chr6:39834833 | A | G | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-21414A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834833 | |||||||
chr6:39834878 | C | T | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-21369C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39834878 | |||||||
chr6:39835005 | C | T | 1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-21242C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835005 | |||||||
chr6:39835032 | C | T | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-21215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835032 | |||||||
chr6:39835039 | C | T | 12 | a0001c0001t0001g0035 a0001c0002t0002g0114 a0001c0002t0002g0192 others(9): Show |
12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-21208C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835039 | |||||||
chr6:39835090 | T | C | 71 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(68): Show |
71 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-56-21157T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835090 | |||||||
chr6:39835148 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-56-21099C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835148 | |||||||
chr6:39835224 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-21023C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835224 | |||||||
chr6:39835352 | A | G | 1 | a0001c0001t0010g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-20895A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835352 | |||||||
chr6:39835411 | C | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-20836C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835411 | |||||||
chr6:39835688 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-56-20559G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835688 | |||||||
chr6:39835692 | C | T | 1 | a0001c0004t0021g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-56-20555C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835692 | |||||||
chr6:39835714 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-20533G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835714 | |||||||
chr6:39835752 | G | A | 4 | a0001c0007t0003g0059 a0001c0007t0013g0208 a0001c0007t0015g0058 others(1): Show |
4 | NA18945.hp1 NA18960.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-20495G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835752 | |||||||
chr6:39835773 | C | A | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-20474C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835773 | |||||||
chr6:39835891 | G | T | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-20356G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39835891 | |||||||
chr6:39836349 | G | A | 76 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(73): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-19898G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836349 | |||||||
chr6:39836373 | C | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-19874C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836373 | |||||||
chr6:39836375 | A | G | 74 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-19872A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836375 | |||||||
chr6:39836404 | G | A | 1 | a0001c0012t0002g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-56-19843G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836404 | |||||||
chr6:39836451 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-19796A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836451 | |||||||
chr6:39836476 | TGAA | T | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-19768_-56-1976 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39836476 | ||||||
chr6:39836558 | A | G | 1 | a0001c0003t0016g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-56-19689A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836558 | |||||||
chr6:39836616 | C | T | 1 | a0008c0038t0009g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-56-19631C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836616 | |||||||
chr6:39836618 | C | G | 2 | a0001c0005t0011g0031 a0001c0009t0009g0128 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56-19629C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836618 | |||||||
chr6:39836684 | A | G | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-19563A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836684 | |||||||
chr6:39836728 | C | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-19519C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836728 | |||||||
chr6:39836881 | T | C | 1 | a0001c0001t0019g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-56-19366T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39836881 | |||||||
chr6:39837087 | A | G | 76 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(73): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-19160A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837087 | |||||||
chr6:39837094 | G | A | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-19153G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837094 | |||||||
chr6:39837203 | A | G | 74 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-19044A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837203 | |||||||
chr6:39837214 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-19033C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837214 | |||||||
chr6:39837215 | G | A | 73 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(70): Show |
73 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-56-19032G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837215 | |||||||
chr6:39837233 | A | T | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-19014A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837233 | |||||||
chr6:39837245 | G | C | 2 | a0001c0005t0003g0291 a0001c0006t0020g0284 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-19002G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837245 | |||||||
chr6:39837335 | G | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(73): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-18912G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837335 | |||||||
chr6:39837339 | T | C | 74 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-18908T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837339 | |||||||
chr6:39837409 | A | G | 5 | a0001c0001t0001g0241 a0001c0001t0032g0243 a0001c0016t0004g0055 others(2): Show |
5 | NA18963.hp2 NA18994.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-18838A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837409 | |||||||
chr6:39837417 | T | C | 12 | a0001c0001t0001g0035 a0001c0002t0002g0114 a0001c0002t0002g0192 others(9): Show |
12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-18830T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837417 | |||||||
chr6:39837446 | T | C | 76 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(73): Show |
76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-56-18801T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837446 | |||||||
chr6:39837492 | G | A | 3 | a0001c0004t0021g0101 a0001c0004t0035g0126 a0001c0008t0005g0102 |
3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-18755G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837492 | |||||||
chr6:39837607 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0280 others(2): Show |
5 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-18640G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837607 | |||||||
chr6:39837650 | C | G | 63 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(60): Show |
63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-18597C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837650 | |||||||
chr6:39837663 | C | CA | 39 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0001g0127 others(36): Show |
39 | HG00741.hp2 HG01169.hp2 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-18561dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAA | 9 | a0001c0001t0001g0124 a0001c0003t0016g0207 a0001c0004t0004g0139 others(6): Show |
9 | HG01081.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-18565_-56-1856 others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAA | 39 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0110 others(36): Show |
39 | HG00438.hp1 HG00609.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.-56-18566_-56-1856 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAAA | 14 | a0001c0001t0001g0035 a0001c0001t0001g0183 a0001c0002t0002g0185 others(11): Show |
14 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-18567_-56-1856 others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAAA others(5): Show |
2 | a0001c0004t0021g0101 a0001c0008t0005g0102 |
2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-56-18572_-56-1856 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0017g0266 |
3 | HG01891.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-56-18575_-56-1856 others(19): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-18576_-56-1856 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | C | CAAAAAAA others(10): Show |
1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-18577_-56-1856 others(21): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837663 | CA | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0230 a0001c0002t0002g0203 others(7): Show |
10 | HG01975.hp2 HG02040.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-18561delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39837663 | ||||||
chr6:39837679 | A | G | 1 | a0001c0001t0010g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-18568A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837679 | |||||||
chr6:39837687 | G | A | 2 | a0001c0001t0001g0273 a0001c0012t0002g0240 |
2 | NA19011.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-56-18560G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837687 | |||||||
chr6:39837692 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-56-18555G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39837692 | |||||||
chr6:39838029 | C | T | 2 | a0001c0005t0003g0291 a0001c0006t0020g0284 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-18218C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838029 | |||||||
chr6:39838446 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-17801C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838446 | |||||||
chr6:39838497 | C | T | 61 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(58): Show |
61 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-56-17750C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838497 | |||||||
chr6:39838649 | C | T | 35 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0137 others(32): Show |
35 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-56-17598C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838649 | |||||||
chr6:39838799 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-17448C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838799 | |||||||
chr6:39838891 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-56-17356G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838891 | |||||||
chr6:39838891 | G | T | 78 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(75): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-56-17356G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838891 | |||||||
chr6:39838899 | C | T | 78 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(75): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-56-17348C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838899 | |||||||
chr6:39838902 | A | AC | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-17342dupC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39838902 | ||||||
chr6:39838963 | CT | C | 63 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(60): Show |
63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-17281delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39838963 | ||||||
chr6:39838983 | G | T | 3 | a0001c0001t0010g0085 a0001c0003t0003g0060 a0002c0015t0003g0217 |
3 | HG00423.hp1 HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-56-17264G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39838983 | |||||||
chr6:39839031 | T | C | 74 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-17216T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839031 | |||||||
chr6:39839032 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-17215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839032 | |||||||
chr6:39839059 | A | G | 2 | a0001c0005t0003g0291 a0001c0006t0020g0284 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-17188A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839059 | |||||||
chr6:39839089 | T | C | 228 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-56-17158T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839089 | |||||||
chr6:39839090 | G | A | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-17157G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839090 | |||||||
chr6:39839090 | G | GT | 6 | a0001c0001t0001g0094 a0001c0001t0001g0213 a0001c0002t0002g0098 others(3): Show |
6 | HG02055.hp1 HG02738.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-17147dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39839090 | ||||||
chr6:39839224 | T | C | 1 | a0001c0003t0003g0198 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-56-17023T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839224 | |||||||
chr6:39839251 | C | T | 2 | a0001c0005t0003g0291 a0001c0006t0020g0284 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-16996C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839251 | |||||||
chr6:39839312 | G | C | 74 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-16935G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839312 | |||||||
chr6:39839319 | T | A | 63 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(60): Show |
63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-56-16928T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839319 | |||||||
chr6:39839515 | G | A | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-16732G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839515 | |||||||
chr6:39839562 | T | G | 2 | a0001c0005t0003g0291 a0001c0006t0020g0284 |
2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-16685T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839562 | |||||||
chr6:39839716 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-16531C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839716 | |||||||
chr6:39839938 | G | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(67): Show |
70 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-56-16309G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39839938 | |||||||
chr6:39840048 | G | A | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-16199G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840048 | |||||||
chr6:39840054 | C | T | 12 | a0001c0001t0001g0035 a0001c0002t0002g0114 a0001c0002t0002g0192 others(9): Show |
12 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-56-16193C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840054 | |||||||
chr6:39840104 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-16143A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840104 | |||||||
chr6:39840119 | C | T | 74 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0076 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-56-16128C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840119 | |||||||
chr6:39840142 | G | A | 59 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(56): Show |
59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-16105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840142 | |||||||
chr6:39840184 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0280 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-56-16063A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840184 | |||||||
chr6:39840229 | A | AAAAC | 10 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0280 others(7): Show |
10 | HG01109.hp1 HG01169.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-15996_-56-1599 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39840229 | ||||||
chr6:39840229 | A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0113 a0001c0005t0011g0031 a0001c0009t0009g0128 |
3 | HG03195.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-56-16000_-56-1599 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39840229 | ||||||
chr6:39840277 | T | C | 1 | a0007c0023t0007g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-56-15970T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840277 | |||||||
chr6:39840288 | C | A | 3 | a0001c0004t0021g0101 a0001c0004t0035g0126 a0001c0008t0005g0102 |
3 | HG01884.hp2 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-15959C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840288 | |||||||
chr6:39840324 | G | A | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-15923G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840324 | |||||||
chr6:39840380 | C | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-15867C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840380 | |||||||
chr6:39840487 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0195 |
2 | HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-56-15760C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840487 | |||||||
chr6:39840771 | G | A | 26 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0184 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.-56-15476G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840771 | |||||||
chr6:39840908 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0074 |
2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-56-15339G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840908 | |||||||
chr6:39840928 | A | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-15319A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39840928 | |||||||
chr6:39841045 | GGCAGGGT others(173): Show |
G | 3 | a0001c0001t0001g0097 a0001c0002t0002g0098 a0001c0003t0003g0010 |
3 | HG02004.hp2 NA19006.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-56-15161_-56-1498 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841045 | ||||||
chr6:39841086 | AGGGGGAG others(173): Show |
A | 67 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(64): Show |
67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-56-15042_-56-1486 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841086 | ||||||
chr6:39841236 | A | G | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-15011A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841236 | |||||||
chr6:39841242 | A | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0194 a0001c0001t0001g0258 others(5): Show |
8 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-15005A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841242 | |||||||
chr6:39841248 | G | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14999G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841248 | |||||||
chr6:39841255 | A | G | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14992A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841255 | |||||||
chr6:39841261 | G | A | 1 | a0001c0003t0007g0002 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-56-14986G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841261 | |||||||
chr6:39841263 | TCCGGGGG others(97): Show |
T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14981_-56-1487 others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39841263 | ||||||
chr6:39841266 | G | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0113 a0001c0001t0001g0154 others(10): Show |
13 | HG01109.hp1 HG01169.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-14981G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841266 | |||||||
chr6:39841378 | G | C | 58 | a0001c0001t0001g0035 a0001c0001t0001g0076 a0001c0001t0001g0077 others(55): Show |
58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-56-14869G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841378 | |||||||
chr6:39841390 | G | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-14857G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841390 | |||||||
chr6:39841420 | G | A | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-14827G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841420 | |||||||
chr6:39841430 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0008g0149 a0001c0002t0002g0133 |
3 | HG01109.hp1 HG01169.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-56-14817G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841430 | |||||||
chr6:39841480 | G | T | 2 | a0001c0003t0003g0117 a0001c0006t0001g0153 |
2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-14767G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841480 | |||||||
chr6:39841484 | C | T | 88 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(85): Show |
88 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-14763C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841484 | |||||||
chr6:39841541 | T | C | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-56-14706T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841541 | |||||||
chr6:39841859 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-14388C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841859 | |||||||
chr6:39841891 | C | T | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-14356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39841891 | |||||||
chr6:39842170 | G | T | 1 | a0001c0003t0003g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-56-14077G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842170 | |||||||
chr6:39842234 | AAGAGCTC others(4): Show |
A | 1 | a0004c0020t0001g0276 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-14010_-56-1400 others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39842234 | ||||||
chr6:39842251 | T | G | 1 | a0006c0040t0002g0229 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-13996T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842251 | |||||||
chr6:39842271 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-56-13976T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842271 | |||||||
chr6:39842279 | G | A | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-13968G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842279 | |||||||
chr6:39842372 | G | A | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-56-13875G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842372 | |||||||
chr6:39842463 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-13784C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842463 | |||||||
chr6:39842489 | C | T | 2 | a0001c0017t0018g0053 a0017c0018t0018g0054 |
2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-13758C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842489 | |||||||
chr6:39842491 | G | T | 10 | a0001c0001t0001g0119 a0001c0002t0002g0277 a0001c0004t0026g0028 others(7): Show |
10 | HG02280.hp1 HG02630.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-13756G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842491 | |||||||
chr6:39842544 | A | G | 2 | a0001c0004t0035g0126 a0001c0008t0005g0102 |
2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-13703A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842544 | |||||||
chr6:39842549 | C | G | 2 | a0001c0004t0035g0126 a0001c0008t0005g0102 |
2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-56-13698C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842549 | |||||||
chr6:39842581 | C | T | 3 | a0001c0001t0036g0224 a0001c0002t0002g0132 a0007c0023t0007g0232 |
3 | HG01934.hp2 HG02004.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-56-13666C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842581 | |||||||
chr6:39842607 | G | A | 1 | a0004c0030t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-56-13640G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842607 | |||||||
chr6:39842690 | G | A | 134 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
135 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.-56-13557G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842690 | |||||||
chr6:39842844 | C | A | 1 | a0001c0006t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-56-13403C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842844 | |||||||
chr6:39842882 | T | C | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-56-13365T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842882 | |||||||
chr6:39842891 | C | T | 10 | a0001c0001t0001g0107 a0001c0001t0001g0204 a0001c0001t0001g0221 others(7): Show |
11 | HG00621.hp2 NA18747.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-13356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39842891 | |||||||
chr6:39843251 | T | C | 1 | a0001c0005t0014g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-56-12996T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843251 | |||||||
chr6:39843280 | A | G | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-12967A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843280 | |||||||
chr6:39843300 | G | A | 1 | a0014c0021t0001g0296 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-56-12947G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843300 | |||||||
chr6:39843381 | G | A | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-12866G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843381 | |||||||
chr6:39843384 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0119 others(42): Show |
45 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-12863G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843384 | |||||||
chr6:39843384 | G | T | 1 | a0001c0045t0002g0164 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-56-12863G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843384 | |||||||
chr6:39843521 | G | T | 1 | a0001c0004t0026g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-56-12726G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843521 | |||||||
chr6:39843525 | G | A | 20 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0209 others(17): Show |
20 | HG01255.hp2 HG01361.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-56-12722G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843525 | |||||||
chr6:39843564 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-56-12683C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843564 | |||||||
chr6:39843569 | C | G | 29 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0251 others(26): Show |
29 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.-56-12678C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843569 | |||||||
chr6:39843626 | T | C | 113 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0076 others(110): Show |
113 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-56-12621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843626 | |||||||
chr6:39843769 | C | T | 29 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0251 others(26): Show |
29 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.-56-12478C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843769 | |||||||
chr6:39843776 | G | C | 175 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0066 others(172): Show |
175 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.-56-12471G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843776 | |||||||
chr6:39843791 | G | C | 208 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0035 others(205): Show |
208 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.-56-12456G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843791 | |||||||
chr6:39843836 | A | T | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-12411A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39843836 | |||||||
chr6:39844037 | A | C | 12 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(9): Show |
12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-12210A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844037 | |||||||
chr6:39844107 | T | G | 159 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(156): Show |
159 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.-56-12140T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844107 | |||||||
chr6:39844329 | C | T | 12 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(9): Show |
12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11918C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844329 | |||||||
chr6:39844371 | G | GAC | 15 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(12): Show |
15 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-11855_-56-1185 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | ||||||
chr6:39844371 | G | GACAC | 32 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0184 others(29): Show |
32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-11857_-56-1185 others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | ||||||
chr6:39844371 | GAC | G | 12 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(9): Show |
12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11855_-56-1185 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844371 | ||||||
chr6:39844411 | C | A | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-56-11836C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844411 | |||||||
chr6:39844517 | C | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(4): Show |
7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-11730C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844517 | |||||||
chr6:39844850 | T | C | 15 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(12): Show |
15 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-11397T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844850 | |||||||
chr6:39844905 | A | G | 156 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(153): Show |
156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-11342A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844905 | |||||||
chr6:39844921 | T | C | 2 | a0001c0032t0009g0169 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-11326T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39844921 | |||||||
chr6:39844983 | CACACACA others(2): Show |
C | 12 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(9): Show |
12 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-11255_-56-1124 others(13): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39844983 | ||||||
chr6:39845232 | G | A | 7 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(4): Show |
7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-11015G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845232 | |||||||
chr6:39845253 | C | T | 1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10994C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845253 | |||||||
chr6:39845254 | G | A | 1 | a0001c0009t0029g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-56-10993G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845254 | |||||||
chr6:39845256 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10991A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845256 | |||||||
chr6:39845275 | A | G | 5 | a0001c0003t0003g0003 a0001c0003t0003g0010 a0001c0003t0003g0136 others(2): Show |
5 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10972A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845275 | |||||||
chr6:39845284 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-56-10963A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845284 | |||||||
chr6:39845326 | CAT | C | 5 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-10919_-56-1091 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845326 | ||||||
chr6:39845345 | T | TCACACAT others(1517): Show |
3 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 |
3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10901_-56-1090 others(1528): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845345 | ||||||
chr6:39845350 | T | C | 3 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 |
3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10897T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845350 | |||||||
chr6:39845364 | G | A | 3 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 |
3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10883G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845364 | |||||||
chr6:39845366 | A | ATACCATA others(356): Show |
3 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 |
3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10881_-56-1088 others(367): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845366 | |||||||
chr6:39845369 | A | AACCCCAT others(1870): Show |
7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1881): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1881): Show |
11 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1892): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1877): Show |
3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0026t0001g0279 |
3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1888): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1891): Show |
1 | a0006c0040t0002g0229 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1882): Show |
1 | a0001c0001t0010g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1893): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1893): Show |
1 | a0001c0007t0003g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1904): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1881): Show |
1 | a0001c0003t0003g0289 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1892): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1891): Show |
1 | a0001c0003t0007g0002 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1891): Show |
9 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(6): Show |
9 | NA18944.hp1 NA18949.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1880): Show |
1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1882): Show |
59 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0040 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1893): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1871): Show |
2 | a0001c0001t0001g0223 a0001c0004t0004g0062 |
2 | NA18960.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1882): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1880): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0230 a0001c0001t0001g0239 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1877): Show |
1 | a0001c0001t0001g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1888): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
45 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1898): Show |
1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1909): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1887): Show |
1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
14 | a0001c0001t0001g0073 a0001c0001t0001g0106 a0001c0001t0001g0127 others(11): Show |
15 | HG01106.hp1 HG01261.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1878): Show |
1 | a0012c0041t0014g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1889): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1885): Show |
1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
2 | a0001c0004t0003g0116 a0009c0019t0003g0037 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1880): Show |
1 | a0001c0002t0038g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1891): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1887): Show |
1 | a0001c0002t0002g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1896): Show |
8 | a0001c0007t0013g0065 a0001c0007t0013g0208 a0001c0007t0013g0245 others(5): Show |
8 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1907): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1891): Show |
1 | a0001c0002t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1902): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1887): Show |
3 | a0001c0002t0002g0039 a0001c0003t0003g0117 a0008c0038t0009g0042 |
3 | HG02109.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0226 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1894): Show |
3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1905): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1887): Show |
1 | a0001c0033t0001g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1898): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
2 | a0004c0020t0001g0276 a0014c0021t0001g0296 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0251 others(3): Show |
6 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
12 | a0001c0001t0019g0051 a0001c0001t0019g0122 a0001c0005t0011g0031 others(9): Show |
12 | HG01081.hp1 HG01361.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1885): Show |
1 | a0001c0001t0001g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1885): Show |
6 | a0001c0001t0001g0124 a0001c0001t0025g0032 a0001c0002t0002g0027 others(3): Show |
6 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1896): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1883): Show |
1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1894): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1872): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0209 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1883): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0010c0047t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0001c0003t0003g0216 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | AACCCCAT others(1889): Show |
1 | a0001c0004t0007g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-56-10876_-56-1087 others(1900): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845369 | ||||||
chr6:39845369 | A | C | 3 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 |
3 | HG02083.hp2 NA18956.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-56-10878A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845369 | |||||||
chr6:39845440 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-56-10807C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845440 | |||||||
chr6:39845441 | G | A | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-10806G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845441 | |||||||
chr6:39845495 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0113 others(42): Show |
45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10752G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845495 | |||||||
chr6:39845514 | A | AC | 6 | a0001c0003t0007g0016 a0001c0004t0021g0061 a0001c0004t0021g0101 others(3): Show |
6 | HG01175.hp1 HG01243.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-10731dupC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39845514 | ||||||
chr6:39845519 | A | G | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10728A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845519 | |||||||
chr6:39845592 | C | G | 2 | a0001c0003t0007g0002 a0006c0040t0002g0229 |
2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-56-10655C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845592 | |||||||
chr6:39845626 | T | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0113 others(42): Show |
45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845626 | |||||||
chr6:39845729 | G | T | 1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-56-10518G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845729 | |||||||
chr6:39845755 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10492G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845755 | |||||||
chr6:39845757 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-56-10490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845757 | |||||||
chr6:39845777 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0113 others(42): Show |
45 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.-56-10470G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845777 | |||||||
chr6:39845784 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-56-10463A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845784 | |||||||
chr6:39845875 | C | T | 1 | a0001c0006t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-56-10372C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845875 | |||||||
chr6:39845920 | A | G | 7 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(4): Show |
7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-10327A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39845920 | |||||||
chr6:39846018 | C | T | 92 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0076 others(89): Show |
92 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-56-10229C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846018 | |||||||
chr6:39846059 | A | G | 3 | a0001c0004t0003g0116 a0001c0033t0001g0045 a0009c0019t0003g0037 |
3 | HG02615.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-56-10188A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846059 | |||||||
chr6:39846207 | C | T | 107 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(104): Show |
107 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-56-10040C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846207 | |||||||
chr6:39846216 | C | T | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-56-10031C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846216 | |||||||
chr6:39846339 | C | A | 2 | a0004c0020t0001g0276 a0014c0021t0001g0296 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-9908C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846339 | |||||||
chr6:39846344 | T | C | 1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-56-9903T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846344 | |||||||
chr6:39846350 | G | A | 5 | a0001c0003t0003g0003 a0001c0003t0003g0010 a0001c0003t0003g0136 others(2): Show |
5 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-9897G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846350 | |||||||
chr6:39846504 | T | C | 156 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(153): Show |
156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-9743T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846504 | |||||||
chr6:39846572 | C | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-56-9675C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846572 | |||||||
chr6:39846633 | C | A | 156 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(153): Show |
156 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.-56-9614C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846633 | |||||||
chr6:39846699 | C | CT | 6 | a0001c0001t0001g0222 a0001c0008t0005g0285 a0001c0013t0023g0170 others(3): Show |
6 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-9533dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | ||||||
chr6:39846699 | CT | C | 106 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0076 others(103): Show |
106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-9533delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | ||||||
chr6:39846699 | CTT | C | 11 | a0001c0001t0001g0182 a0001c0003t0003g0198 a0001c0004t0006g0075 others(8): Show |
11 | NA18747.hp1 NA18939.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-9534_-56-9533d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39846699 | ||||||
chr6:39846727 | C | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0119 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-56-9520C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846727 | |||||||
chr6:39846728 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-56-9519G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846728 | |||||||
chr6:39846733 | G | T | 1 | a0001c0002t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-56-9514G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846733 | |||||||
chr6:39846947 | C | T | 1 | a0001c0006t0001g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-9300C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39846947 | |||||||
chr6:39847157 | G | A | 3 | a0001c0001t0001g0181 a0001c0002t0002g0020 a0001c0002t0002g0021 |
3 | NA18963.hp1 NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-9090G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847157 | |||||||
chr6:39847290 | G | A | 1 | a0001c0004t0004g0197 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-56-8957G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847290 | |||||||
chr6:39847306 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-8941C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847306 | |||||||
chr6:39847333 | G | C | 1 | a0001c0001t0010g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56-8914G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847333 | |||||||
chr6:39847396 | G | C | 14 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8851G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847396 | |||||||
chr6:39847409 | G | A | 14 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(11): Show |
14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8838G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847409 | |||||||
chr6:39847454 | G | C | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-56-8793G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847454 | |||||||
chr6:39847654 | C | T | 2 | a0001c0001t0019g0051 a0001c0001t0019g0122 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-56-8593C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847654 | |||||||
chr6:39847655 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-56-8592G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847655 | |||||||
chr6:39847797 | C | A | 14 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(11): Show |
14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8450C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847797 | |||||||
chr6:39847819 | C | T | 88 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0076 others(85): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-8428C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847819 | |||||||
chr6:39847836 | C | G | 14 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(11): Show |
14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-8411C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847836 | |||||||
chr6:39847987 | G | A | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-8260G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39847987 | |||||||
chr6:39848013 | A | G | 6 | a0001c0002t0002g0046 a0001c0002t0002g0098 a0001c0002t0002g0237 others(3): Show |
6 | HG00423.hp2 NA18971.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-8234A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848013 | |||||||
chr6:39848137 | C | T | 2 | a0001c0032t0009g0169 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-56-8110C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848137 | |||||||
chr6:39848142 | CTTCA | C | 7 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(4): Show |
7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-8102_-56-8099d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39848142 | ||||||
chr6:39848157 | T | C | 32 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0119 others(29): Show |
32 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-56-8090T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848157 | |||||||
chr6:39848240 | C | T | 1 | a0001c0022t0020g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-56-8007C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848240 | |||||||
chr6:39848357 | T | C | 59 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0156 others(56): Show |
59 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.-56-7890T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848357 | |||||||
chr6:39848428 | CTT | C | 3 | a0001c0016t0004g0055 a0001c0017t0018g0053 a0017c0018t0018g0054 |
3 | NA18994.hp2 NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-56-7817_-56-7816d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39848428 | ||||||
chr6:39848531 | T | C | 1 | a0001c0033t0001g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-7716T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848531 | |||||||
chr6:39848537 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-56-7710G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848537 | |||||||
chr6:39848543 | C | T | 1 | a0001c0008t0005g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-56-7704C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848543 | |||||||
chr6:39848545 | T | C | 14 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(11): Show |
14 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-56-7702T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848545 | |||||||
chr6:39848617 | G | A | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-7630G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848617 | |||||||
chr6:39848858 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0274 |
2 | NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-56-7389T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848858 | |||||||
chr6:39848865 | C | A | 1 | a0001c0004t0031g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-56-7382C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848865 | |||||||
chr6:39848891 | G | A | 88 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0094 others(85): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-56-7356G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848891 | |||||||
chr6:39848929 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0119 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-56-7318C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848929 | |||||||
chr6:39848959 | C | T | 1 | a0001c0007t0015g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-56-7288C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39848959 | |||||||
chr6:39849008 | T | TG | 4 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-7236dupG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39849008 | ||||||
chr6:39849122 | C | G | 1 | a0001c0002t0002g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-56-7125C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849122 | |||||||
chr6:39849395 | G | A | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-6852G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849395 | |||||||
chr6:39849407 | G | T | 1 | a0006c0040t0002g0229 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-6840G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849407 | |||||||
chr6:39849536 | T | C | 106 | a0001c0001t0001g0023 a0001c0001t0001g0066 a0001c0001t0001g0094 others(103): Show |
106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-56-6711T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849536 | |||||||
chr6:39849777 | G | T | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-56-6470G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849777 | |||||||
chr6:39849982 | C | T | 1 | a0001c0003t0003g0129 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-56-6265C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39849982 | |||||||
chr6:39850029 | T | TCCCAGC | 56 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(53): Show |
56 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.-56-6206_-56-6201d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39850029 | ||||||
chr6:39850029 | T | TCCCAGCC others(5): Show |
13 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(10): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-6212_-56-6201d others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr6 | 39850029 | ||||||
chr6:39850124 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0251 others(10): Show |
13 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-56-6123C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850124 | |||||||
chr6:39850239 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-6008C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850239 | |||||||
chr6:39850399 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0165 a0001c0001t0001g0230 others(1): Show |
4 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-5848C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850399 | |||||||
chr6:39850439 | T | G | 2 | a0001c0003t0007g0016 a0001c0031t0040g0143 |
2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-56-5808T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850439 | |||||||
chr6:39850509 | G | A | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-5738G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850509 | |||||||
chr6:39850598 | T | C | 161 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(158): Show |
161 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-5649T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850598 | |||||||
chr6:39850665 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-56-5582C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850665 | |||||||
chr6:39850889 | G | A | 2 | a0001c0001t0001g0190 a0001c0005t0037g0063 |
2 | NA19007.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-56-5358G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39850889 | |||||||
chr6:39851088 | T | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(21): Show |
24 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.-56-5159T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851088 | |||||||
chr6:39851231 | G | A | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-56-5016G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851231 | |||||||
chr6:39851368 | T | A | 10 | a0001c0007t0003g0059 a0001c0007t0013g0065 a0001c0007t0013g0083 others(7): Show |
10 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-4879T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851368 | |||||||
chr6:39851388 | G | T | 1 | a0001c0004t0006g0142 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-56-4859G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851388 | |||||||
chr6:39851430 | A | C | 4 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-4817A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851430 | |||||||
chr6:39851758 | C | A | 2 | a0004c0020t0001g0276 a0014c0021t0001g0296 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-4489C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851758 | |||||||
chr6:39851760 | C | T | 3 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0024 |
3 | HG04228.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-56-4487C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851760 | |||||||
chr6:39851761 | G | A | 2 | a0001c0003t0003g0177 a0001c0004t0003g0103 |
2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-56-4486G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851761 | |||||||
chr6:39851777 | G | A | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-4470G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851777 | |||||||
chr6:39851811 | C | G | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-4436C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39851811 | |||||||
chr6:39852125 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-4122C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852125 | |||||||
chr6:39852187 | G | A | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-56-4060G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852187 | |||||||
chr6:39852587 | G | A | 10 | a0001c0007t0003g0059 a0001c0007t0013g0065 a0001c0007t0013g0083 others(7): Show |
10 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-3660G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852587 | |||||||
chr6:39852644 | A | G | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-3603A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852644 | |||||||
chr6:39852703 | C | T | 5 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3544C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852703 | |||||||
chr6:39852774 | A | G | 1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-3473A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39852774 | |||||||
chr6:39853039 | T | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0209 a0001c0001t0019g0051 others(1): Show |
4 | HG01255.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-3208T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853039 | |||||||
chr6:39853142 | G | A | 2 | a0001c0014t0001g0030 a0001c0014t0017g0265 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-56-3105G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853142 | |||||||
chr6:39853224 | T | A | 9 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-3023T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853224 | |||||||
chr6:39853579 | C | T | 161 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0066 others(158): Show |
161 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-2668C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853579 | |||||||
chr6:39853752 | T | A | 18 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-2495T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853752 | |||||||
chr6:39853764 | C | G | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-56-2483C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853764 | |||||||
chr6:39853895 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0209 a0001c0001t0019g0051 others(1): Show |
4 | HG01255.hp2 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-2352A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853895 | |||||||
chr6:39853965 | C | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0251 others(10): Show |
13 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-56-2282C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39853965 | |||||||
chr6:39854268 | G | A | 2 | a0001c0014t0001g0030 a0001c0014t0017g0265 |
2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-56-1979G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854268 | |||||||
chr6:39854317 | T | G | 13 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(10): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-1930T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854317 | |||||||
chr6:39854343 | A | G | 172 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(169): Show |
173 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-1904A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854343 | |||||||
chr6:39854395 | G | A | 5 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-1852G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854395 | |||||||
chr6:39854407 | T | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0106 others(17): Show |
21 | HG00735.hp1 HG01106.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-1840T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854407 | |||||||
chr6:39854413 | T | C | 4 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 others(1): Show |
4 | HG02451.hp1 HG03516.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1834T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854413 | |||||||
chr6:39854443 | G | A | 185 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(182): Show |
186 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.-56-1804G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854443 | |||||||
chr6:39854648 | G | T | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1599G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854648 | |||||||
chr6:39854958 | A | G | 1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-56-1289A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854958 | |||||||
chr6:39854966 | G | A | 30 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(27): Show |
30 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-56-1281G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39854966 | |||||||
chr6:39855422 | A | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-56-825A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855422 | |||||||
chr6:39855425 | C | T | 9 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56-822C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855425 | |||||||
chr6:39855443 | A | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-56-804A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855443 | |||||||
chr6:39855448 | C | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-56-799C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855448 | |||||||
chr6:39855525 | C | G | 4 | a0001c0004t0004g0071 a0002c0010t0002g0096 a0002c0010t0002g0235 others(1): Show |
4 | HG02015.hp2 HG02027.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-722C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855525 | |||||||
chr6:39855768 | C | T | 13 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(10): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-479C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855768 | |||||||
chr6:39855831 | G | C | 1 | a0001c0003t0039g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-56-416G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855831 | |||||||
chr6:39855863 | T | C | 1 | a0001c0002t0002g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-56-384T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855863 | |||||||
chr6:39855892 | T | G | 45 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-56-355T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855892 | |||||||
chr6:39855895 | G | A | 1 | a0001c0012t0002g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-56-352G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855895 | |||||||
chr6:39855962 | C | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(19): Show |
22 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-56-285C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 1/24 | chr6 | 39855962 | |||||||
chr6:39856649 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.168+179T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856649 | |||||||
chr6:39856765 | A | C | 13 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(10): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+295A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856765 | |||||||
chr6:39856791 | G | T | 166 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(163): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.168+321G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856791 | |||||||
chr6:39856872 | A | G | 9 | a0001c0001t0001g0182 a0001c0003t0003g0198 a0001c0004t0004g0206 others(6): Show |
9 | NA18939.hp1 NA18939.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+402A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856872 | |||||||
chr6:39856905 | G | T | 13 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(10): Show |
13 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.168+435G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39856905 | |||||||
chr6:39857029 | T | C | 9 | a0001c0001t0019g0051 a0001c0001t0019g0122 a0001c0005t0011g0031 others(6): Show |
9 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+559T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857029 | |||||||
chr6:39857066 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0119 others(18): Show |
21 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.168+596G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857066 | |||||||
chr6:39857102 | G | A | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.168+632G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857102 | |||||||
chr6:39857132 | C | T | 1 | a0001c0005t0004g0082 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.168+662C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857132 | |||||||
chr6:39857303 | A | G | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+833A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857303 | |||||||
chr6:39857584 | A | G | 1 | a0005c0028t0004g0290 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.168+1114A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857584 | |||||||
chr6:39857744 | G | C | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1274G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857744 | |||||||
chr6:39857771 | C | T | 4 | a0001c0007t0003g0059 a0001c0007t0013g0065 a0001c0007t0013g0208 others(1): Show |
4 | NA18945.hp1 NA18956.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1301C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857771 | |||||||
chr6:39857799 | G | C | 9 | a0001c0007t0003g0059 a0001c0007t0013g0065 a0001c0007t0013g0208 others(6): Show |
9 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+1329G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857799 | |||||||
chr6:39857868 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+1398C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857868 | |||||||
chr6:39857869 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.168+1399T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39857869 | |||||||
chr6:39858090 | G | T | 13 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0181 others(10): Show |
13 | HG02083.hp2 NA18944.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+1620G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858090 | |||||||
chr6:39858108 | C | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+1638C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858108 | |||||||
chr6:39858154 | G | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.168+1684G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858154 | |||||||
chr6:39858460 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.168+1990A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858460 | |||||||
chr6:39858491 | G | T | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168+2021G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858491 | |||||||
chr6:39858684 | C | T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0010 a0001c0003t0003g0136 others(3): Show |
6 | HG01943.hp2 HG01952.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+2214C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858684 | |||||||
chr6:39858767 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.169-2161G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39858767 | |||||||
chr6:39859047 | A | T | 9 | a0001c0007t0003g0059 a0001c0007t0013g0065 a0001c0007t0013g0208 others(6): Show |
9 | NA18944.hp2 NA18945.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-1881A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859047 | |||||||
chr6:39859714 | A | G | 222 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(219): Show |
223 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.169-1214A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859714 | |||||||
chr6:39859951 | TAA | T | 8 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-975_169-974del others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr6 | 39859951 | ||||||
chr6:39859958 | T | G | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-970T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859958 | |||||||
chr6:39859966 | T | G | 7 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(4): Show |
7 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-962T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39859966 | |||||||
chr6:39860028 | A | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(168): Show |
172 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.169-900A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860028 | |||||||
chr6:39860031 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.169-897C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860031 | |||||||
chr6:39860263 | T | C | 1 | a0001c0002t0002g0144 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.169-665T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860263 | |||||||
chr6:39860301 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.169-627A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860301 | |||||||
chr6:39860342 | C | T | 1 | a0001c0002t0002g0120 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169-586C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860342 | |||||||
chr6:39860405 | A | G | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.169-523A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860405 | |||||||
chr6:39860432 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0233 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-496G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860432 | |||||||
chr6:39860503 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.169-425A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860503 | |||||||
chr6:39860817 | A | T | 138 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(135): Show |
139 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.169-111A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860817 | |||||||
chr6:39860853 | A | G | 1 | a0001c0004t0006g0075 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.169-75A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 2/24 | chr6 | 39860853 | |||||||
chr6:39861039 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0233 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+22G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861039 | |||||||
chr6:39861048 | C | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.258+31C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861048 | |||||||
chr6:39861086 | A | C | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.258+69A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861086 | |||||||
chr6:39861094 | G | A | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258+77G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861094 | |||||||
chr6:39861101 | C | A | 1 | a0001c0026t0001g0279 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+84C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861101 | |||||||
chr6:39861339 | T | C | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+322T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861339 | |||||||
chr6:39861340 | G | A | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.258+323G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861340 | |||||||
chr6:39861362 | G | T | 4 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+345G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861362 | |||||||
chr6:39861447 | T | C | 182 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(179): Show |
183 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.258+430T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861447 | |||||||
chr6:39861499 | G | A | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+482G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861499 | |||||||
chr6:39861692 | G | T | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+675G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861692 | |||||||
chr6:39861772 | C | A | 1 | a0001c0003t0003g0289 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.258+755C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861772 | |||||||
chr6:39861897 | C | G | 1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.258+880C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39861897 | |||||||
chr6:39862040 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0118 a0001c0001t0001g0194 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1023C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862040 | |||||||
chr6:39862042 | A | G | 7 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(4): Show |
7 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+1025A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862042 | |||||||
chr6:39862148 | G | A | 1 | a0001c0005t0006g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.258+1131G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862148 | |||||||
chr6:39862160 | C | T | 1 | a0001c0002t0002g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.258+1143C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862160 | |||||||
chr6:39862486 | A | C | 1 | a0001c0004t0007g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258+1469A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862486 | |||||||
chr6:39862493 | AAAAC | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0194 a0001c0001t0001g0280 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1496_258+1499d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862493 | ||||||
chr6:39862513 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.258+1496C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862513 | |||||||
chr6:39862541 | T | C | 181 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(178): Show |
182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.258+1524T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862541 | |||||||
chr6:39862753 | C | T | 3 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0029g0174 |
3 | HG02630.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.259-1680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862753 | |||||||
chr6:39862791 | G | A | 2 | a0001c0001t0001g0220 a0013c0034t0001g0231 |
2 | HG01515.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.259-1642G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862791 | |||||||
chr6:39862792 | C | T | 1 | a0001c0002t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.259-1641C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862792 | |||||||
chr6:39862805 | C | CA | 34 | a0001c0001t0001g0156 a0001c0001t0001g0182 a0001c0002t0002g0046 others(31): Show |
34 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-1597dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | C | CAA | 15 | a0001c0001t0001g0213 a0001c0002t0002g0009 a0001c0002t0002g0019 others(12): Show |
15 | HG00438.hp2 HG01123.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1598_259-1597d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CA | C | 19 | a0001c0001t0001g0094 a0001c0002t0002g0021 a0001c0002t0002g0108 others(16): Show |
19 | HG01361.hp2 HG02818.hp1 HG02922.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-1597delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAA | C | 16 | a0001c0001t0001g0066 a0001c0004t0004g0038 a0001c0004t0004g0047 others(13): Show |
16 | HG01884.hp1 HG02083.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1598_259-1597d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAA | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0086 others(14): Show |
17 | HG00423.hp1 HG01123.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.259-1599_259-1597d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAAA | C | 125 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0023 others(122): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.259-1600_259-1597d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAAAA | C | 34 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0073 others(31): Show |
34 | HG00741.hp2 HG01081.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-1601_259-1597d others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAAAAA | C | 6 | a0001c0008t0005g0292 a0001c0009t0009g0112 a0001c0009t0009g0128 others(3): Show |
6 | HG02630.hp1 HG02895.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1602_259-1597d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAAAAAA others(6): Show |
C | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1609_259-1597d others(15): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862805 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.259-1612_259-1597d others(18): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39862805 | ||||||
chr6:39862811 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0209 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.259-1622A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39862811 | |||||||
chr6:39863112 | C | T | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-1321C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863112 | |||||||
chr6:39863224 | G | A | 1 | a0006c0040t0002g0229 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.259-1209G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863224 | |||||||
chr6:39863260 | A | G | 15 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(12): Show |
15 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-1173A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863260 | |||||||
chr6:39863363 | T | A | 1 | a0001c0004t0031g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.259-1070T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863363 | |||||||
chr6:39863691 | A | G | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(167): Show |
171 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.259-742A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863691 | |||||||
chr6:39863902 | A | C | 10 | a0001c0002t0002g0039 a0001c0003t0003g0117 a0001c0004t0003g0116 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-531A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39863902 | |||||||
chr6:39864094 | G | T | 1 | a0001c0002t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.259-339G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864094 | |||||||
chr6:39864164 | TA | T | 7 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(4): Show |
7 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-263delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 39864164 | ||||||
chr6:39864221 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.259-212C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864221 | |||||||
chr6:39864335 | A | G | 175 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(172): Show |
176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.259-98A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 3/24 | chr6 | 39864335 | |||||||
chr6:39864587 | C | A | 7 | a0001c0004t0004g0206 a0001c0004t0006g0075 a0001c0004t0006g0090 others(4): Show |
7 | NA18939.hp2 NA18945.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+80C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864587 | |||||||
chr6:39864587 | C | G | 226 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(223): Show |
227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.333+80C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864587 | |||||||
chr6:39864774 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.334-206G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 4/24 | chr6 | 39864774 | |||||||
chr6:39865116 | A | G | 3 | a0001c0002t0002g0039 a0001c0003t0003g0117 a0008c0038t0009g0042 |
3 | HG02109.hp2 HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.428+42A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865116 | |||||||
chr6:39865188 | T | C | 211 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(208): Show |
212 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.428+114T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865188 | |||||||
chr6:39865227 | C | T | 1 | a0001c0002t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.428+153C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865227 | |||||||
chr6:39865430 | C | T | 5 | a0001c0008t0005g0102 a0001c0008t0005g0166 a0001c0008t0005g0285 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865430 | |||||||
chr6:39865462 | C | G | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.428+388C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865462 | |||||||
chr6:39865486 | C | T | 11 | a0001c0006t0001g0041 a0001c0006t0001g0153 a0001c0006t0001g0159 others(8): Show |
11 | HG00741.hp2 HG02486.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+412C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865486 | |||||||
chr6:39865547 | G | A | 1 | a0001c0009t0009g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.428+473G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865547 | |||||||
chr6:39865551 | T | C | 1 | a0001c0004t0004g0197 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.428+477T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865551 | |||||||
chr6:39865631 | G | A | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+557G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865631 | |||||||
chr6:39865695 | T | C | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(176): Show |
180 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.428+621T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865695 | |||||||
chr6:39865898 | C | T | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+824C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865898 | |||||||
chr6:39865911 | T | C | 2 | a0001c0002t0002g0145 a0001c0002t0002g0262 |
2 | HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.428+837T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39865911 | |||||||
chr6:39866142 | C | T | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+1068C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866142 | |||||||
chr6:39866235 | A | G | 225 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(222): Show |
226 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.428+1161A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866235 | |||||||
chr6:39866313 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(3): Show |
6 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1197T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866313 | |||||||
chr6:39866365 | TA | T | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-1138delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr6 | 39866365 | ||||||
chr6:39866366 | A | G | 1 | a0001c0003t0003g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.429-1144A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866366 | |||||||
chr6:39866373 | T | C | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-1137T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866373 | |||||||
chr6:39866393 | G | C | 53 | a0001c0001t0001g0156 a0001c0001t0001g0213 a0001c0001t0001g0273 others(50): Show |
53 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.429-1117G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866393 | |||||||
chr6:39866430 | G | A | 1 | a0001c0012t0002g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.429-1080G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866430 | |||||||
chr6:39866461 | A | G | 4 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 others(1): Show |
4 | HG02922.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-1049A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866461 | |||||||
chr6:39866538 | A | G | 178 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(175): Show |
179 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.429-972A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866538 | |||||||
chr6:39866559 | T | C | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-951T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866559 | |||||||
chr6:39866610 | A | G | 57 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(54): Show |
57 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.429-900A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866610 | |||||||
chr6:39866615 | G | T | 1 | a0001c0037t0002g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429-895G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866615 | |||||||
chr6:39866621 | C | A | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.429-889C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866621 | |||||||
chr6:39866809 | G | A | 1 | a0001c0004t0006g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.429-701G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866809 | |||||||
chr6:39866936 | T | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0110 a0001c0001t0010g0085 |
3 | HG02015.hp1 HG02523.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.429-574T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39866936 | |||||||
chr6:39867456 | AGT | A | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-51_429-50delGT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr6 | 39867456 | ||||||
chr6:39867500 | T | C | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-10T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 5/24 | chr6 | 39867500 | |||||||
chr6:39867936 | T | G | 1 | a0010c0047t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.762+93T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39867936 | |||||||
chr6:39867978 | G | C | 1 | a0001c0001t0008g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.762+135G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39867978 | |||||||
chr6:39868020 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.762+177T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868020 | |||||||
chr6:39868072 | T | C | 144 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(141): Show |
145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.762+229T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868072 | |||||||
chr6:39868076 | T | C | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.762+233T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868076 | |||||||
chr6:39868331 | G | A | 222 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(219): Show |
223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.762+488G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868331 | |||||||
chr6:39868495 | T | G | 222 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(219): Show |
223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.763-328T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868495 | |||||||
chr6:39868605 | G | A | 1 | a0001c0032t0009g0169 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.763-218G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868605 | |||||||
chr6:39868681 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.763-142G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868681 | |||||||
chr6:39868799 | G | A | 11 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(8): Show |
11 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.763-24G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 6/24 | chr6 | 39868799 | |||||||
chr6:39868997 | A | T | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0026t0001g0279 |
3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.873+64A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39868997 | |||||||
chr6:39869014 | A | G | 8 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(5): Show |
8 | HG02895.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.873+81A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869014 | |||||||
chr6:39869060 | C | A | 1 | a0001c0002t0002g0254 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.873+127C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869060 | |||||||
chr6:39869063 | C | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.873+130C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869063 | |||||||
chr6:39869200 | C | T | 17 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0001g0074 others(14): Show |
17 | HG01433.hp1 HG01496.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.873+267C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869200 | |||||||
chr6:39869307 | G | A | 1 | a0001c0003t0003g0008 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.873+374G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869307 | |||||||
chr6:39869310 | C | T | 1 | a0001c0003t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.873+377C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869310 | |||||||
chr6:39869325 | C | T | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.873+392C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869325 | |||||||
chr6:39869421 | C | T | 9 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.873+488C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869421 | |||||||
chr6:39869443 | C | T | 33 | a0001c0001t0001g0234 a0001c0001t0010g0018 a0001c0003t0003g0003 others(30): Show |
33 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.873+510C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869443 | |||||||
chr6:39869519 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0074 |
2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.873+586G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869519 | |||||||
chr6:39869576 | G | A | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.873+643G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869576 | |||||||
chr6:39869601 | C | A | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.873+668C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869601 | |||||||
chr6:39869666 | T | C | 1 | a0001c0004t0035g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.874-674T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869666 | |||||||
chr6:39869753 | C | CT | 15 | a0001c0001t0001g0066 a0001c0001t0001g0273 a0001c0002t0002g0019 others(12): Show |
15 | HG00642.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.874-560dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CT | C | 70 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0184 others(67): Show |
70 | HG00423.hp1 HG00621.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.874-560delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CTT | C | 80 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0023 others(77): Show |
81 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.874-561_874-560del others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CTTT | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0074 others(9): Show |
12 | HG01433.hp1 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.874-562_874-560del others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CTTTTTT | C | 7 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(4): Show |
7 | HG02922.hp1 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.874-565_874-560del others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CTTTTTTT others(1): Show |
C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0233 others(13): Show |
16 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.874-567_874-560del others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869753 | CTTTTTTT others(6): Show |
C | 1 | a0001c0006t0001g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.874-572_874-560del others(13): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869753 | ||||||
chr6:39869755 | T | G | 2 | a0001c0001t0019g0051 a0001c0001t0019g0122 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.874-585T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869755 | |||||||
chr6:39869756 | T | G | 5 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.874-584T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869756 | |||||||
chr6:39869780 | T | A | 3 | a0001c0002t0002g0253 a0001c0003t0003g0111 a0001c0003t0003g0269 |
3 | HG02040.hp1 NA18952.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.874-560T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869780 | |||||||
chr6:39869780 | T | TTA | 8 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(5): Show |
8 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.874-560_874-559ins others(2): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869780 | |||||||
chr6:39869781 | A | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.874-559A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869781 | |||||||
chr6:39869804 | TG | T | 14 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(11): Show |
14 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-533delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr6 | 39869804 | ||||||
chr6:39869905 | T | G | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-435T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39869905 | |||||||
chr6:39870105 | G | A | 3 | a0001c0005t0004g0064 a0001c0005t0004g0082 a0001c0005t0004g0212 |
3 | NA18952.hp2 NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.874-235G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39870105 | |||||||
chr6:39870127 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.874-213A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 7/24 | chr6 | 39870127 | |||||||
chr6:39870506 | T | C | 1 | a0001c0002t0002g0253 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.977+63T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870506 | |||||||
chr6:39870585 | G | A | 3 | a0001c0002t0002g0039 a0001c0003t0003g0117 a0001c0006t0001g0033 |
3 | HG02451.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.977+142G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870585 | |||||||
chr6:39870621 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.977+178C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870621 | |||||||
chr6:39870693 | G | C | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.977+250G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870693 | |||||||
chr6:39870720 | C | T | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.977+277C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870720 | |||||||
chr6:39870849 | C | T | 40 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0086 others(37): Show |
40 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.977+406C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39870849 | |||||||
chr6:39871230 | T | C | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.978-276T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871230 | |||||||
chr6:39871232 | A | T | 1 | a0001c0033t0001g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.978-274A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871232 | |||||||
chr6:39871291 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0124 others(22): Show |
25 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.978-215C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871291 | |||||||
chr6:39871311 | G | A | 1 | a0001c0036t0022g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.978-195G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871311 | |||||||
chr6:39871388 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.978-118T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 8/24 | chr6 | 39871388 | |||||||
chr6:39871596 | G | A | 3 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 |
3 | HG02970.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1044+24G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871596 | |||||||
chr6:39871651 | C | T | 1 | a0001c0022t0020g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044+79C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871651 | |||||||
chr6:39871675 | G | A | 1 | a0001c0002t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1044+103G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871675 | |||||||
chr6:39871681 | T | G | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+109T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39871681 | |||||||
chr6:39872033 | C | T | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+461C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872033 | |||||||
chr6:39872228 | C | A | 10 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044+656C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872228 | |||||||
chr6:39872286 | A | G | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+714A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872286 | |||||||
chr6:39872298 | A | G | 1 | a0005c0029t0001g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1044+726A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872298 | |||||||
chr6:39872306 | C | T | 1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1044+734C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872306 | |||||||
chr6:39872387 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0010g0268 |
2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1044+815G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872387 | |||||||
chr6:39872747 | G | A | 1 | a0001c0002t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1045-491G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872747 | |||||||
chr6:39872816 | G | T | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1045-422G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872816 | |||||||
chr6:39872833 | T | TG | 180 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(177): Show |
181 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1045-405_1045-404i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872833 | |||||||
chr6:39872899 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0226 |
2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1045-339A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872899 | |||||||
chr6:39872922 | T | C | 3 | a0001c0003t0003g0179 a0001c0003t0003g0198 a0001c0003t0003g0201 |
3 | HG00621.hp1 HG03017.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1045-316T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39872922 | |||||||
chr6:39873060 | T | C | 3 | a0001c0003t0016g0123 a0001c0003t0016g0207 a0001c0003t0016g0283 |
3 | HG02717.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1045-178T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873060 | |||||||
chr6:39873061 | A | C | 1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1045-177A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873061 | |||||||
chr6:39873125 | G | A | 1 | a0003c0024t0001g0029 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1045-113G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873125 | |||||||
chr6:39873206 | C | T | 8 | a0001c0005t0014g0176 a0001c0006t0001g0041 a0001c0006t0001g0153 others(5): Show |
8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1045-32C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873206 | |||||||
chr6:39873214 | T | A | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1045-24T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 9/24 | chr6 | 39873214 | |||||||
chr6:39873929 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1162+574A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39873929 | |||||||
chr6:39874222 | A | G | 180 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(177): Show |
181 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1162+867A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874222 | |||||||
chr6:39874607 | T | C | 15 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(12): Show |
15 | HG00741.hp2 HG01361.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1163-723T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874607 | |||||||
chr6:39874658 | C | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1163-672C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874658 | |||||||
chr6:39874685 | C | A | 2 | a0001c0004t0003g0116 a0009c0019t0003g0037 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1163-645C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874685 | |||||||
chr6:39874686 | A | G | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1163-644A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874686 | |||||||
chr6:39874719 | A | G | 38 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0001t0001g0088 others(35): Show |
38 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1163-611A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874719 | |||||||
chr6:39874907 | T | G | 1 | a0001c0001t0001g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1163-423T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39874907 | |||||||
chr6:39875004 | T | C | 1 | a0001c0002t0002g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1163-326T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875004 | |||||||
chr6:39875073 | A | C | 1 | a0001c0008t0005g0026 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1163-257A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875073 | |||||||
chr6:39875138 | C | T | 167 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(164): Show |
168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1163-192C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 10/24 | chr6 | 39875138 | |||||||
chr6:39875510 | C | G | 1 | a0001c0002t0002g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1301+42C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875510 | |||||||
chr6:39875575 | C | T | 1 | a0001c0002t0002g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1301+107C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875575 | |||||||
chr6:39875634 | A | G | 8 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(5): Show |
8 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301+166A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875634 | |||||||
chr6:39875739 | C | A | 221 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
222 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1301+271C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875739 | |||||||
chr6:39875821 | G | A | 8 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0025g0032 others(5): Show |
8 | HG02895.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1301+353G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39875821 | |||||||
chr6:39876446 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1301+978T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876446 | |||||||
chr6:39876504 | C | G | 2 | a0001c0032t0009g0169 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1301+1036C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876504 | |||||||
chr6:39876523 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1301+1055C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876523 | |||||||
chr6:39876557 | G | A | 1 | a0001c0002t0002g0187 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1301+1089G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876557 | |||||||
chr6:39876706 | GGTGTGT | G | 3 | a0003c0011t0001g0004 a0003c0011t0001g0006 a0003c0011t0001g0007 |
3 | HG02970.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1301+1256_1301+126 others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876706 | ||||||
chr6:39876722 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1301+1254T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876722 | |||||||
chr6:39876724 | T | TGC | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0025t0034g0299 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1257_1301+125 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876724 | ||||||
chr6:39876726 | T | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0124 others(30): Show |
33 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1301+1258T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876726 | |||||||
chr6:39876726 | T | TGC | 186 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(183): Show |
187 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1301+1259_1301+126 others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr6 | 39876726 | ||||||
chr6:39876728 | T | C | 1 | a0001c0002t0002g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1301+1260T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876728 | |||||||
chr6:39876730 | C | T | 221 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
222 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1301+1262C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876730 | |||||||
chr6:39876786 | T | C | 1 | a0001c0002t0002g0024 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1301+1318T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876786 | |||||||
chr6:39876810 | C | T | 10 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301+1342C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876810 | |||||||
chr6:39876844 | C | G | 8 | a0001c0005t0014g0176 a0001c0006t0001g0041 a0001c0006t0001g0153 others(5): Show |
8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302-1359C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876844 | |||||||
chr6:39876887 | G | A | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-1316G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876887 | |||||||
chr6:39876942 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
225 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.1302-1261T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39876942 | |||||||
chr6:39877022 | A | C | 1 | a0001c0007t0013g0065 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1302-1181A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877022 | |||||||
chr6:39877033 | A | G | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-1170A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877033 | |||||||
chr6:39877068 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1302-1135C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877068 | |||||||
chr6:39877170 | C | G | 1 | a0001c0002t0002g0260 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1302-1033C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877170 | |||||||
chr6:39877769 | G | A | 3 | a0001c0004t0003g0116 a0001c0033t0001g0045 a0009c0019t0003g0037 |
3 | HG02615.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1302-434G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877769 | |||||||
chr6:39877802 | G | T | 1 | a0001c0004t0031g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1302-401G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877802 | |||||||
chr6:39877855 | G | A | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1302-348G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39877855 | |||||||
chr6:39878012 | C | A | 1 | a0001c0045t0002g0164 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1302-191C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39878012 | |||||||
chr6:39878161 | T | A | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1302-42T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 11/24 | chr6 | 39878161 | |||||||
chr6:39878326 | C | T | 1 | a0001c0007t0012g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1360+65C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878326 | |||||||
chr6:39878333 | C | G | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1361-71C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878333 | |||||||
chr6:39878361 | A | G | 194 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(191): Show |
195 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1361-43A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 12/24 | chr6 | 39878361 | |||||||
chr6:39878765 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0251 a0001c0001t0001g0258 |
3 | HG01175.hp2 HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1545+177G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878765 | |||||||
chr6:39878799 | G | C | 222 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(219): Show |
223 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1545+211G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878799 | |||||||
chr6:39878914 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0195 a0001c0001t0001g0233 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-264G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878914 | |||||||
chr6:39878940 | A | G | 29 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0124 others(26): Show |
29 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-238A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878940 | |||||||
chr6:39878959 | C | T | 1 | a0001c0003t0003g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1546-219C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39878959 | |||||||
chr6:39879083 | T | C | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1546-95T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 13/24 | chr6 | 39879083 | |||||||
chr6:39879503 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0073 others(17): Show |
21 | HG00323.hp1 HG00735.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1845+26G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879503 | |||||||
chr6:39879696 | A | C | 4 | a0001c0004t0003g0103 a0001c0004t0003g0116 a0001c0033t0001g0045 others(1): Show |
4 | HG02257.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+219A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879696 | |||||||
chr6:39879902 | A | C | 19 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.1845+425A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39879902 | |||||||
chr6:39880018 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1845+541G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880018 | |||||||
chr6:39880333 | C | T | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+856C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880333 | |||||||
chr6:39880402 | C | T | 36 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(33): Show |
36 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1845+925C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880402 | |||||||
chr6:39880542 | C | T | 1 | a0001c0003t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1845+1065C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880542 | |||||||
chr6:39880543 | A | G | 226 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(223): Show |
227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1845+1066A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880543 | |||||||
chr6:39880645 | TG | T | 36 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0002t0002g0108 others(33): Show |
36 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1845+1169delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880645 | |||||||
chr6:39880656 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1845+1179C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880656 | |||||||
chr6:39880758 | C | T | 10 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(7): Show |
10 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845+1281C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880758 | |||||||
chr6:39880946 | G | A | 8 | a0001c0005t0014g0176 a0001c0006t0001g0041 a0001c0006t0001g0153 others(5): Show |
8 | HG00741.hp2 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1845+1469G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39880946 | |||||||
chr6:39881104 | G | A | 4 | a0001c0002t0002g0145 a0001c0002t0002g0157 a0001c0002t0002g0249 others(1): Show |
4 | HG00099.hp2 HG00642.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1845+1627G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881104 | |||||||
chr6:39881239 | AG | A | 143 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(140): Show |
144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1845+1763delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881239 | |||||||
chr6:39881297 | C | T | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1845+1820C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881297 | |||||||
chr6:39881298 | G | A | 11 | a0001c0004t0007g0236 a0001c0007t0003g0059 a0001c0007t0012g0079 others(8): Show |
11 | HG02735.hp1 NA18747.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1845+1821G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881298 | |||||||
chr6:39881393 | T | G | 223 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(220): Show |
224 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1845+1916T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881393 | |||||||
chr6:39881441 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0124 others(29): Show |
32 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1845+1964G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881441 | |||||||
chr6:39881488 | G | A | 1 | a0001c0022t0020g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1845+2011G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881488 | |||||||
chr6:39881489 | C | T | 1 | a0001c0009t0029g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1845+2012C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881489 | |||||||
chr6:39881554 | T | TA | 37 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0124 others(34): Show |
37 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1845+2082dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39881554 | ||||||
chr6:39881585 | C | T | 5 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1845+2108C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881585 | |||||||
chr6:39881645 | G | A | 2 | a0001c0001t0001g0258 a0001c0003t0003g0155 |
2 | HG02738.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1845+2168G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881645 | |||||||
chr6:39881873 | G | A | 1 | a0001c0005t0003g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1846-2089G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39881873 | |||||||
chr6:39882199 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0127 others(3): Show |
6 | HG00323.hp1 HG01106.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1846-1763C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882199 | |||||||
chr6:39882216 | T | C | 2 | a0001c0004t0035g0126 a0005c0029t0001g0178 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1846-1746T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882216 | |||||||
chr6:39882333 | G | T | 9 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1846-1629G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882333 | |||||||
chr6:39882393 | A | C | 1 | a0001c0044t0022g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1846-1569A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882393 | |||||||
chr6:39882497 | T | C | 23 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(20): Show |
23 | HG01884.hp1 HG01891.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1846-1465T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882497 | |||||||
chr6:39882522 | T | C | 196 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(193): Show |
197 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1846-1440T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882522 | |||||||
chr6:39882560 | G | C | 219 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
220 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1846-1402G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882560 | |||||||
chr6:39882702 | C | T | 3 | a0001c0002t0002g0148 a0001c0006t0001g0015 a0001c0006t0001g0135 |
3 | HG01358.hp2 HG02738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1846-1260C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882702 | |||||||
chr6:39882703 | GCACACAC others(3): Show |
G | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
211 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1846-1253_1846-124 others(14): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39882703 | ||||||
chr6:39882719 | GCACACAC others(1): Show |
G | 9 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1846-1236_1846-122 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39882719 | ||||||
chr6:39882732 | C | T | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1846-1230C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882732 | |||||||
chr6:39882798 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1846-1164C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882798 | |||||||
chr6:39882852 | G | T | 1 | a0001c0002t0002g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1846-1110G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882852 | |||||||
chr6:39882867 | G | C | 194 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(191): Show |
195 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1846-1095G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882867 | |||||||
chr6:39882943 | G | A | 20 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(17): Show |
20 | HG02083.hp2 HG02129.hp1 HG04184.hp2 others(17): Show |
intron_variant | MODIFIER | c.1846-1019G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39882943 | |||||||
chr6:39883028 | G | A | 19 | a0001c0002t0002g0148 a0001c0004t0003g0103 a0001c0004t0031g0293 others(16): Show |
19 | HG00741.hp2 HG01081.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1846-934G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883028 | |||||||
chr6:39883089 | T | C | 4 | a0001c0008t0005g0166 a0001c0008t0005g0285 a0001c0008t0024g0034 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-873T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883089 | |||||||
chr6:39883184 | CTT | C | 17 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0001g0113 others(14): Show |
17 | HG00621.hp2 HG02055.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1846-763_1846-762d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39883184 | ||||||
chr6:39883184 | CTTT | C | 215 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(212): Show |
216 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1846-764_1846-762d others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr6 | 39883184 | ||||||
chr6:39883202 | G | T | 3 | a0001c0009t0009g0163 a0001c0014t0001g0030 a0001c0014t0017g0265 |
3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1846-760G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883202 | |||||||
chr6:39883203 | C | G | 1 | a0001c0003t0003g0289 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1846-759C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883203 | |||||||
chr6:39883264 | C | A | 3 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0026t0001g0279 |
3 | HG01884.hp1 HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1846-698C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883264 | |||||||
chr6:39883502 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0025 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1846-460C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883502 | |||||||
chr6:39883571 | G | A | 4 | a0001c0013t0023g0170 a0001c0013t0023g0171 a0001c0026t0001g0279 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1846-391G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883571 | |||||||
chr6:39883623 | C | T | 2 | a0001c0007t0012g0079 a0001c0007t0012g0080 |
2 | NA18747.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1846-339C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883623 | |||||||
chr6:39883665 | G | C | 237 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(234): Show |
238 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.1846-297G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883665 | |||||||
chr6:39883685 | A | G | 10 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1846-277A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883685 | |||||||
chr6:39883903 | A | G | 115 | a0001c0002t0002g0009 a0001c0002t0002g0019 a0001c0002t0002g0020 others(112): Show |
115 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1846-59A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 14/24 | chr6 | 39883903 | |||||||
chr6:39884261 | T | C | 158 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(155): Show |
159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1953+192T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884261 | |||||||
chr6:39884287 | G | A | 67 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0025 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1953+218G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884287 | |||||||
chr6:39884506 | T | C | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+437T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884506 | |||||||
chr6:39884618 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1953+549A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884618 | |||||||
chr6:39884626 | G | GCTGGGC | 11 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(8): Show |
11 | HG02109.hp2 NA18747.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1953+575_1953+580d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39884626 | ||||||
chr6:39884626 | GCTGGGC | G | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+575_1953+580d others(8): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39884626 | ||||||
chr6:39884645 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1953+576C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884645 | |||||||
chr6:39884662 | A | G | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+593A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884662 | |||||||
chr6:39884759 | C | T | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+690C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884759 | |||||||
chr6:39884802 | T | C | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+733T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884802 | |||||||
chr6:39884831 | T | G | 1 | a0001c0022t0020g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1953+762T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884831 | |||||||
chr6:39884857 | G | A | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+788G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884857 | |||||||
chr6:39884908 | C | T | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+839C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39884908 | |||||||
chr6:39885074 | A | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1953+1005A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885074 | |||||||
chr6:39885144 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0086 others(7): Show |
10 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1953+1075C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885144 | |||||||
chr6:39885174 | T | C | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1953+1105T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885174 | |||||||
chr6:39885177 | C | T | 1 | a0001c0004t0004g0038 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1953+1108C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885177 | |||||||
chr6:39885188 | T | A | 28 | a0001c0002t0002g0148 a0001c0005t0011g0031 a0001c0005t0011g0043 others(25): Show |
28 | HG00741.hp2 HG01081.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1953+1119T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885188 | |||||||
chr6:39885189 | G | A | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1120G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885189 | |||||||
chr6:39885189 | G | T | 6 | a0001c0002t0002g0132 a0001c0002t0002g0133 a0001c0002t0002g0146 others(3): Show |
6 | HG01109.hp1 HG01169.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1953+1120G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885189 | |||||||
chr6:39885346 | T | TA | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1277_1953+127 others(5): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885346 | |||||||
chr6:39885363 | G | A | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1294G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885363 | |||||||
chr6:39885382 | TG | T | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1317delG | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39885382 | ||||||
chr6:39885413 | C | T | 25 | a0001c0004t0003g0103 a0001c0004t0004g0038 a0001c0004t0004g0047 others(22): Show |
25 | HG02083.hp2 HG02129.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1953+1344C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885413 | |||||||
chr6:39885414 | A | G | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1345A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885414 | |||||||
chr6:39885588 | G | A | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1953+1519G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885588 | |||||||
chr6:39885655 | T | G | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1953+1586T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885655 | |||||||
chr6:39885666 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1953+1597G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885666 | |||||||
chr6:39885667 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1953+1598C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885667 | |||||||
chr6:39885778 | T | C | 1 | a0001c0004t0007g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1954-1708T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885778 | |||||||
chr6:39885795 | T | A | 159 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(156): Show |
160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1954-1691T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885795 | |||||||
chr6:39885853 | A | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0086 others(7): Show |
10 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1954-1633A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885853 | |||||||
chr6:39885868 | A | T | 6 | a0001c0002t0002g0027 a0001c0002t0002g0039 a0001c0002t0002g0277 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1954-1618A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885868 | |||||||
chr6:39885874 | G | A | 25 | a0001c0004t0003g0103 a0001c0004t0004g0038 a0001c0004t0004g0047 others(22): Show |
25 | HG02083.hp2 HG02129.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1954-1612G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885874 | |||||||
chr6:39885879 | G | A | 4 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 others(1): Show |
4 | HG02451.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-1607G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39885879 | |||||||
chr6:39886022 | A | G | 1 | a0008c0038t0009g0042 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1954-1464A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886022 | |||||||
chr6:39886170 | C | T | 4 | a0001c0005t0004g0064 a0001c0005t0004g0082 a0001c0005t0004g0212 others(1): Show |
4 | NA18952.hp2 NA19011.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-1316C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886170 | |||||||
chr6:39886186 | G | T | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1954-1300G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886186 | |||||||
chr6:39886187 | G | A | 1 | a0001c0003t0003g0252 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1954-1299G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886187 | |||||||
chr6:39886202 | C | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1954-1284C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886202 | |||||||
chr6:39886301 | T | C | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1954-1185T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886301 | |||||||
chr6:39886469 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1954-1017G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886469 | |||||||
chr6:39886649 | A | G | 239 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(236): Show |
240 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.1954-837A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886649 | |||||||
chr6:39886884 | C | T | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1954-602C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886884 | |||||||
chr6:39886885 | G | A | 5 | a0001c0002t0002g0027 a0001c0002t0002g0039 a0001c0002t0002g0277 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1954-601G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39886885 | |||||||
chr6:39887125 | G | T | 193 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(190): Show |
194 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1954-361G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887125 | |||||||
chr6:39887224 | A | C | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
185 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1954-262A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887224 | |||||||
chr6:39887240 | T | TA | 10 | a0001c0007t0003g0059 a0001c0007t0012g0079 a0001c0007t0012g0080 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.1954-238dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr6 | 39887240 | ||||||
chr6:39887243 | A | C | 183 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(180): Show |
184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1954-243A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887243 | |||||||
chr6:39887315 | G | A | 4 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 others(1): Show |
4 | HG02451.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1954-171G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887315 | |||||||
chr6:39887336 | T | G | 198 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(195): Show |
199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1954-150T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887336 | |||||||
chr6:39887428 | G | A | 1 | a0001c0004t0003g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1954-58G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 15/24 | chr6 | 39887428 | |||||||
chr6:39887651 | C | T | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
148 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2060+59C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887651 | |||||||
chr6:39887714 | C | CTGGA | 146 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
147 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.2060+123_2060+126d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr6 | 39887714 | ||||||
chr6:39887810 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2060+218C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887810 | |||||||
chr6:39887953 | G | A | 1 | a0001c0002t0002g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2060+361G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39887953 | |||||||
chr6:39888002 | A | G | 1 | a0001c0008t0005g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2060+410A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888002 | |||||||
chr6:39888172 | C | T | 7 | a0001c0004t0004g0206 a0001c0004t0006g0075 a0001c0004t0006g0090 others(4): Show |
7 | NA18939.hp2 NA18945.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.2061-507C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888172 | |||||||
chr6:39888380 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0025 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2061-299G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888380 | |||||||
chr6:39888611 | C | T | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2061-68C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 16/24 | chr6 | 39888611 | |||||||
chr6:39888775 | C | T | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2145+12C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888775 | |||||||
chr6:39888804 | G | A | 4 | a0001c0008t0005g0166 a0001c0008t0005g0285 a0001c0008t0024g0034 others(1): Show |
4 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+41G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888804 | |||||||
chr6:39888863 | A | G | 1 | a0001c0002t0002g0263 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2145+100A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888863 | |||||||
chr6:39888913 | A | G | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2145+150A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39888913 | |||||||
chr6:39889092 | T | A | 54 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(51): Show |
54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.2145+329T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889092 | |||||||
chr6:39889146 | A | G | 1 | a0001c0012t0002g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2145+383A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889146 | |||||||
chr6:39889210 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2145+447G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889210 | |||||||
chr6:39889534 | A | G | 4 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(1): Show |
4 | HG02083.hp2 NA18956.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+771A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889534 | |||||||
chr6:39889537 | C | T | 1 | a0001c0002t0002g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2145+774C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889537 | |||||||
chr6:39889545 | TA | T | 10 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2145+783delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889545 | |||||||
chr6:39889550 | A | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0023 others(22): Show |
26 | HG00323.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2145+787A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889550 | |||||||
chr6:39889633 | G | A | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2145+870G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889633 | |||||||
chr6:39889710 | G | A | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
148 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2145+947G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889710 | |||||||
chr6:39889746 | A | G | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2145+983A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889746 | |||||||
chr6:39889819 | C | T | 16 | a0001c0001t0001g0105 a0001c0001t0001g0118 a0001c0001t0001g0194 others(13): Show |
16 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2145+1056C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39889819 | |||||||
chr6:39890125 | C | CA | 148 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(145): Show |
149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2146-1207dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39890125 | ||||||
chr6:39890155 | C | T | 215 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(212): Show |
216 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.2146-1186C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890155 | |||||||
chr6:39890325 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0089 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2146-1016C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890325 | |||||||
chr6:39890508 | T | C | 1 | a0001c0005t0004g0064 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2146-833T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890508 | |||||||
chr6:39890536 | G | C | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2146-805G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890536 | |||||||
chr6:39890688 | A | C | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2146-653A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890688 | |||||||
chr6:39890718 | T | C | 5 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2146-623T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890718 | |||||||
chr6:39890965 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2146-376A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890965 | |||||||
chr6:39890991 | C | T | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2146-350C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39890991 | |||||||
chr6:39891027 | C | T | 2 | a0001c0001t0001g0281 a0001c0001t0017g0266 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2146-314C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891027 | |||||||
chr6:39891090 | T | TA | 148 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(145): Show |
149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2146-236dupA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39891090 | ||||||
chr6:39891090 | TA | T | 12 | a0001c0002t0002g0019 a0001c0002t0002g0246 a0001c0004t0007g0236 others(9): Show |
12 | HG02027.hp2 HG02735.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.2146-236delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr6 | 39891090 | ||||||
chr6:39891315 | G | A | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2146-26G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891315 | |||||||
chr6:39891326 | G | A | 45 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2146-15G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 17/24 | chr6 | 39891326 | |||||||
chr6:39891476 | AGCAGGTG others(17): Show |
A | 2 | a0001c0003t0039g0091 a0012c0041t0014g0147 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2252+40_2252+63del others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr6 | 39891476 | ||||||
chr6:39891611 | G | T | 53 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(50): Show |
53 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2253-23G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 18/24 | chr6 | 39891611 | |||||||
chr6:39891745 | G | A | 3 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 |
3 | NA18747.hp1 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2341+23G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891745 | |||||||
chr6:39891865 | C | G | 10 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2341+143C>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891865 | |||||||
chr6:39891891 | T | C | 64 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(61): Show |
64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2341+169T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891891 | |||||||
chr6:39891921 | C | A | 1 | a0001c0004t0004g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2341+199C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891921 | |||||||
chr6:39891972 | G | A | 3 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0022t0020g0048 |
3 | HG02451.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2341+250G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39891972 | |||||||
chr6:39892074 | T | C | 56 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2341+352T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892074 | |||||||
chr6:39892108 | C | T | 10 | a0001c0007t0012g0079 a0001c0007t0012g0080 a0001c0007t0012g0081 others(7): Show |
10 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.2341+386C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892108 | |||||||
chr6:39892109 | T | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2341+387T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892109 | |||||||
chr6:39892143 | A | G | 2 | a0001c0017t0018g0053 a0017c0018t0018g0054 |
2 | NA18997.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2341+421A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892143 | |||||||
chr6:39892154 | G | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2341+432G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892154 | |||||||
chr6:39892173 | G | A | 1 | a0001c0003t0016g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2341+451G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892173 | |||||||
chr6:39892254 | C | T | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2341+532C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892254 | |||||||
chr6:39892294 | A | G | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2341+572A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892294 | |||||||
chr6:39892305 | A | G | 35 | a0001c0004t0003g0103 a0001c0004t0004g0038 a0001c0004t0004g0047 others(32): Show |
35 | HG01884.hp2 HG02055.hp2 HG02083.hp2 others(32): Show |
intron_variant | MODIFIER | c.2341+583A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892305 | |||||||
chr6:39892317 | C | T | 122 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2341+595C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892317 | |||||||
chr6:39892335 | A | C | 61 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0025 others(58): Show |
61 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2341+613A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892335 | |||||||
chr6:39892377 | G | A | 74 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(71): Show |
74 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2341+655G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892377 | |||||||
chr6:39892990 | A | G | 1 | a0001c0007t0013g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2341+1268A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39892990 | |||||||
chr6:39893078 | C | T | 1 | a0001c0008t0005g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2341+1356C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893078 | |||||||
chr6:39893181 | G | A | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0025 others(60): Show |
63 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.2341+1459G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893181 | |||||||
chr6:39893281 | C | T | 1 | a0001c0003t0016g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2341+1559C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893281 | |||||||
chr6:39893291 | C | A | 1 | a0001c0005t0006g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2341+1569C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893291 | |||||||
chr6:39893358 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0274 |
2 | NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2341+1636A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893358 | |||||||
chr6:39893366 | A | C | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2341+1644A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893366 | |||||||
chr6:39893399 | T | C | 1 | a0001c0012t0002g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2341+1677T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893399 | |||||||
chr6:39893402 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0251 a0001c0001t0001g0258 |
3 | HG01175.hp2 HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2341+1680C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893402 | |||||||
chr6:39893450 | G | A | 18 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(15): Show |
18 | HG01361.hp2 HG02109.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2341+1728G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893450 | |||||||
chr6:39893553 | T | C | 29 | a0001c0004t0003g0103 a0001c0004t0012g0099 a0001c0007t0012g0079 others(26): Show |
29 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.2341+1831T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893553 | |||||||
chr6:39893625 | G | A | 3 | a0001c0006t0020g0284 a0001c0006t0027g0189 a0001c0022t0020g0048 |
3 | HG02486.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2341+1903G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893625 | |||||||
chr6:39893642 | T | A | 1 | a0001c0002t0002g0144 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2341+1920T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893642 | |||||||
chr6:39893743 | G | A | 28 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(25): Show |
28 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.2341+2021G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893743 | |||||||
chr6:39893819 | G | A | 48 | a0001c0002t0002g0009 a0001c0002t0002g0019 a0001c0002t0002g0022 others(45): Show |
48 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.2341+2097G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893819 | |||||||
chr6:39893904 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0010g0268 |
2 | HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2341+2182G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39893904 | |||||||
chr6:39894016 | C | T | 61 | a0001c0002t0002g0185 a0001c0003t0003g0003 a0001c0003t0003g0008 others(58): Show |
62 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2341+2294C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894016 | |||||||
chr6:39894030 | ATTC | A | 6 | a0001c0009t0009g0112 a0001c0009t0009g0128 a0001c0009t0009g0163 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2341+2314_2341+231 others(7): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39894030 | ||||||
chr6:39894203 | G | A | 1 | a0001c0005t0004g0050 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2341+2481G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894203 | |||||||
chr6:39894297 | C | T | 1 | a0010c0047t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2342-2515C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894297 | |||||||
chr6:39894406 | G | C | 3 | a0004c0020t0001g0276 a0004c0030t0001g0193 a0014c0021t0001g0296 |
3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2342-2406G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894406 | |||||||
chr6:39894473 | A | C | 1 | a0001c0001t0033g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2342-2339A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894473 | |||||||
chr6:39894501 | C | A | 5 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2342-2311C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894501 | |||||||
chr6:39894596 | G | A | 1 | a0001c0001t0017g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2342-2216G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | |||||||
chr6:39894596 | G | C | 63 | a0001c0002t0002g0185 a0001c0003t0003g0003 a0001c0003t0003g0008 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-2216G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | |||||||
chr6:39894596 | G | T | 1 | a0001c0003t0003g0104 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2342-2216G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894596 | |||||||
chr6:39894604 | A | G | 3 | a0001c0003t0014g0087 a0001c0003t0014g0211 a0001c0005t0014g0176 |
3 | HG02818.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2342-2208A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894604 | |||||||
chr6:39894623 | T | A | 64 | a0001c0002t0002g0185 a0001c0003t0003g0003 a0001c0003t0003g0008 others(61): Show |
65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2342-2189T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894623 | |||||||
chr6:39894630 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2342-2182T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894630 | |||||||
chr6:39894650 | C | T | 64 | a0001c0002t0002g0185 a0001c0003t0003g0003 a0001c0003t0003g0008 others(61): Show |
65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2342-2162C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894650 | |||||||
chr6:39894685 | ATCTTGGC others(17): Show |
A | 5 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(2): Show |
5 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2342-2124_2342-210 others(28): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39894685 | ||||||
chr6:39894819 | A | G | 1 | a0001c0006t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2342-1993A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39894819 | |||||||
chr6:39895158 | T | C | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1654T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895158 | |||||||
chr6:39895218 | C | CTTTATTT others(5): Show |
2 | a0001c0005t0004g0064 a0001c0005t0004g0212 |
2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2342-1586_2342-158 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895218 | ||||||
chr6:39895218 | CTTTATTT others(5): Show |
C | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1585_2342-157 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895218 | ||||||
chr6:39895227 | C | CTTACTTA others(5): Show |
11 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0086 others(8): Show |
11 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2342-1582_2342-158 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTACTTA others(9): Show |
2 | a0001c0001t0001g0012 a0001c0006t0001g0294 |
2 | HG01993.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2342-1582_2342-158 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTATTTA others(1): Show |
26 | a0001c0001t0001g0119 a0001c0001t0001g0239 a0001c0001t0008g0215 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2342-1566_2342-155 others(12): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTATTTA others(5): Show |
66 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0070 others(63): Show |
66 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.2342-1570_2342-155 others(16): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTATTTA others(9): Show |
42 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0040 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.2342-1574_2342-155 others(20): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTATTTA others(13): Show |
15 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0066 others(12): Show |
15 | HG01891.hp1 HG02559.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.2342-1578_2342-155 others(24): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | CTTATTTA others(17): Show |
1 | a0001c0001t0001g0274 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2342-1582_2342-155 others(28): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39895227 | ||||||
chr6:39895227 | C | T | 2 | a0001c0005t0004g0064 a0001c0005t0004g0212 |
2 | NA19011.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2342-1585C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895227 | |||||||
chr6:39895259 | G | A | 1 | a0001c0003t0014g0211 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2342-1553G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895259 | |||||||
chr6:39895345 | C | T | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2342-1467C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895345 | |||||||
chr6:39895435 | C | T | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1377C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895435 | |||||||
chr6:39895436 | G | A | 1 | a0001c0001t0008g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2342-1376G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895436 | |||||||
chr6:39895441 | A | G | 241 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
242 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2342-1371A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895441 | |||||||
chr6:39895451 | T | G | 201 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(198): Show |
202 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.2342-1361T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895451 | |||||||
chr6:39895456 | G | C | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1356G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895456 | |||||||
chr6:39895478 | T | C | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1334T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895478 | |||||||
chr6:39895519 | T | A | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1293T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895519 | |||||||
chr6:39895576 | G | A | 2 | a0001c0001t0019g0051 a0001c0001t0019g0122 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2342-1236G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895576 | |||||||
chr6:39895692 | C | T | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-1120C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895692 | |||||||
chr6:39895703 | G | T | 3 | a0001c0003t0003g0036 a0001c0003t0003g0057 a0001c0003t0003g0069 |
3 | HG01975.hp1 NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2342-1109G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895703 | |||||||
chr6:39895791 | C | T | 1 | a0001c0004t0004g0052 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2342-1021C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895791 | |||||||
chr6:39895828 | A | C | 11 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(8): Show |
11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2342-984A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895828 | |||||||
chr6:39895831 | T | C | 6 | a0001c0003t0003g0060 a0001c0003t0003g0155 a0001c0003t0003g0179 others(3): Show |
6 | HG00423.hp1 HG00621.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2342-981T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895831 | |||||||
chr6:39895852 | C | CCA | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-960_2342-959i others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895852 | |||||||
chr6:39895853 | A | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-959A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895853 | |||||||
chr6:39895857 | A | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-955A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895857 | |||||||
chr6:39895858 | G | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-954G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895858 | |||||||
chr6:39895859 | A | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-953A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895859 | |||||||
chr6:39895860 | G | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-952G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895860 | |||||||
chr6:39895863 | T | A | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-949T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895863 | |||||||
chr6:39895866 | G | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-946G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895866 | |||||||
chr6:39895867 | G | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-945G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895867 | |||||||
chr6:39895868 | G | C | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-944G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895868 | |||||||
chr6:39895869 | G | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-943G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895869 | |||||||
chr6:39895872 | AAT | A | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-939_2342-938d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895872 | |||||||
chr6:39895875 | G | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2342-937G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895875 | |||||||
chr6:39895959 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0094 a0001c0001t0001g0110 |
3 | HG02015.hp1 NA18966.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2342-853C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39895959 | |||||||
chr6:39896018 | T | G | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-794T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896018 | |||||||
chr6:39896038 | A | ATT | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-767_2342-766d others(4): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896038 | ||||||
chr6:39896062 | A | G | 27 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(24): Show |
27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2342-750A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896062 | |||||||
chr6:39896071 | A | T | 1 | a0001c0009t0029g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2342-741A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896071 | |||||||
chr6:39896082 | A | C | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-730A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896082 | |||||||
chr6:39896087 | C | T | 1 | a0001c0007t0015g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2342-725C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896087 | |||||||
chr6:39896182 | A | G | 2 | a0001c0013t0023g0170 a0001c0013t0023g0171 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2342-630A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896182 | |||||||
chr6:39896194 | T | TTTTTTTC | 150 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(147): Show |
150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2342-598_2342-592d others(9): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896194 | ||||||
chr6:39896194 | T | TTTTTTTT others(1): Show |
26 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2342-612_2342-611i others(10): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 39896194 | ||||||
chr6:39896333 | T | G | 200 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(197): Show |
201 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.2342-479T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896333 | |||||||
chr6:39896396 | G | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2342-416G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896396 | |||||||
chr6:39896406 | G | A | 70 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(67): Show |
71 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2342-406G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896406 | |||||||
chr6:39896424 | G | A | 3 | a0001c0006t0001g0294 a0001c0014t0001g0030 a0001c0014t0017g0265 |
3 | HG02280.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2342-388G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896424 | |||||||
chr6:39896449 | T | C | 241 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
242 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.2342-363T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896449 | |||||||
chr6:39896517 | T | G | 3 | a0002c0010t0002g0096 a0002c0010t0002g0235 a0002c0010t0002g0255 |
3 | HG02015.hp2 HG02027.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2342-295T>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896517 | |||||||
chr6:39896536 | A | G | 1 | a0001c0003t0003g0129 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2342-276A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896536 | |||||||
chr6:39896740 | T | C | 38 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(35): Show |
39 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.2342-72T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896740 | |||||||
chr6:39896781 | G | A | 63 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(60): Show |
64 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2342-31G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896781 | |||||||
chr6:39896802 | C | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2342-10C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 19/24 | chr6 | 39896802 | |||||||
chr6:39896988 | C | T | 4 | a0001c0005t0011g0031 a0001c0005t0011g0043 a0001c0005t0011g0093 others(1): Show |
4 | HG02280.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2510+8C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/24 | chr6 | 39896988 | |||||||
chr6:39897090 | TC | T | 3 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 |
3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2511-84delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 20/24 | chr6 | 39897090 | |||||||
chr6:39897423 | A | C | 1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2618+141A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897423 | |||||||
chr6:39897596 | A | C | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2618+314A>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897596 | |||||||
chr6:39897743 | G | GT | 11 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(8): Show |
11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2618+468dupT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39897743 | ||||||
chr6:39897865 | T | C | 3 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 |
3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2618+583T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897865 | |||||||
chr6:39897894 | G | C | 13 | a0001c0002t0002g0046 a0001c0002t0002g0098 a0001c0002t0002g0180 others(10): Show |
13 | HG02015.hp2 HG02027.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2618+612G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39897894 | |||||||
chr6:39898168 | G | A | 27 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(24): Show |
27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2619-709G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898168 | |||||||
chr6:39898183 | A | T | 1 | a0001c0009t0009g0163 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2619-694A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898183 | |||||||
chr6:39898234 | GCAAT | G | 4 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(1): Show |
4 | NA18747.hp1 NA18954.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.2619-640_2619-637d others(6): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39898234 | ||||||
chr6:39898347 | G | A | 229 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
230 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.2619-530G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898347 | |||||||
chr6:39898416 | A | AGCATCTG others(14): Show |
1 | a0001c0003t0003g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2619-460_2619-440d others(23): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr6 | 39898416 | ||||||
chr6:39898494 | G | T | 1 | a0001c0025t0034g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2619-383G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898494 | |||||||
chr6:39898514 | G | A | 129 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(126): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.2619-363G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898514 | |||||||
chr6:39898580 | T | C | 1 | a0001c0012t0002g0297 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2619-297T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 21/24 | chr6 | 39898580 | |||||||
chr6:39898993 | C | T | 27 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(24): Show |
27 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.2679+56C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39898993 | |||||||
chr6:39898994 | G | A | 1 | a0001c0003t0003g0036 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2679+57G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39898994 | |||||||
chr6:39899029 | A | AACAATGG others(2): Show |
230 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(227): Show |
231 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.2679+100_2679+101i others(11): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr6 | 39899029 | ||||||
chr6:39899132 | C | T | 3 | a0004c0020t0001g0276 a0004c0030t0001g0193 a0014c0021t0001g0296 |
3 | HG01081.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2679+195C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899132 | |||||||
chr6:39899229 | A | G | 3 | a0001c0001t0010g0017 a0001c0001t0010g0018 a0001c0001t0010g0085 |
3 | HG02523.hp2 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2679+292A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899229 | |||||||
chr6:39899243 | T | C | 3 | a0001c0004t0021g0061 a0001c0004t0021g0101 a0001c0004t0031g0293 |
3 | HG02451.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2679+306T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899243 | |||||||
chr6:39899271 | G | A | 26 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2679+334G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899271 | |||||||
chr6:39899290 | G | C | 11 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(8): Show |
11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2679+353G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899290 | |||||||
chr6:39899347 | G | A | 11 | a0001c0004t0012g0099 a0001c0007t0012g0079 a0001c0007t0012g0080 others(8): Show |
11 | NA18747.hp1 NA18944.hp2 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.2679+410G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899347 | |||||||
chr6:39899391 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2679+454C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899391 | |||||||
chr6:39899399 | A | G | 5 | a0001c0006t0001g0041 a0001c0006t0001g0159 a0001c0006t0020g0284 others(2): Show |
5 | HG00741.hp2 HG02486.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679+462A>G | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899399 | |||||||
chr6:39899674 | C | T | 1 | a0001c0002t0002g0237 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2680-403C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899674 | |||||||
chr6:39899949 | GA | G | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-127delA | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899949 | |||||||
chr6:39899953 | T | A | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-124T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899953 | |||||||
chr6:39899954 | GC | G | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-122delC | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899954 | |||||||
chr6:39899960 | T | A | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-117T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899960 | |||||||
chr6:39899961 | G | A | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-116G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899961 | |||||||
chr6:39899962 | T | C | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-115T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899962 | |||||||
chr6:39899963 | T | A | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-114T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899963 | |||||||
chr6:39899967 | T | TG | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-110_2680-109i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899967 | |||||||
chr6:39899969 | T | A | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-108T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899969 | |||||||
chr6:39899971 | C | CT | 49 | a0001c0003t0003g0003 a0001c0003t0003g0008 a0001c0003t0003g0010 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2680-106_2680-105i others(3): Show |
DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39899971 | |||||||
chr6:39900021 | G | C | 3 | a0001c0007t0013g0065 a0001c0007t0013g0208 a0001c0007t0013g0245 |
3 | NA18945.hp1 NA18956.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2680-56G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900021 | |||||||
chr6:39900027 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2680-50G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900027 | |||||||
chr6:39900052 | G | A | 1 | a0001c0006t0001g0015 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2680-25G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 22/24 | chr6 | 39900052 | |||||||
chr6:39900260 | G | A | 26 | a0001c0004t0004g0038 a0001c0004t0004g0047 a0001c0004t0004g0052 others(23): Show |
26 | HG00423.hp2 HG00609.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.2811+52G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900260 | |||||||
chr6:39900298 | G | A | 7 | a0001c0003t0003g0036 a0001c0003t0003g0057 a0001c0003t0003g0069 others(4): Show |
7 | HG00438.hp1 HG01975.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.2811+90G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900298 | |||||||
chr6:39900305 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2811+97C>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900305 | |||||||
chr6:39900321 | T | C | 2 | a0001c0036t0022g0168 a0001c0044t0022g0115 |
2 | HG01361.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2811+113T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900321 | |||||||
chr6:39900547 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2811+339T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900547 | |||||||
chr6:39900598 | A | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2811+390A>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900598 | |||||||
chr6:39900600 | G | T | 1 | a0001c0046t0001g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2811+392G>T | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900600 | |||||||
chr6:39900642 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0230 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2811+434G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900642 | |||||||
chr6:39900698 | T | A | 1 | a0005c0029t0001g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2811+490T>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900698 | |||||||
chr6:39900746 | CT | C | 197 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(194): Show |
198 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2811+542delT | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr6 | 39900746 | ||||||
chr6:39900877 | C | A | 3 | a0001c0001t0001g0113 a0003c0011t0001g0004 a0003c0011t0001g0007 |
3 | HG02970.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2812-425C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900877 | |||||||
chr6:39900988 | T | C | 9 | a0001c0008t0005g0026 a0001c0008t0005g0102 a0001c0008t0005g0166 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2812-314T>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39900988 | |||||||
chr6:39901099 | C | A | 7 | a0001c0003t0003g0008 a0001c0003t0003g0060 a0001c0003t0003g0155 others(4): Show |
7 | HG00423.hp1 HG00621.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.2812-203C>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39901099 | |||||||
chr6:39901290 | G | C | 199 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(196): Show |
200 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.2812-12G>C | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 23/24 | chr6 | 39901290 | |||||||
chr6:39901805 | G | A | 1 | a0001c0008t0005g0167 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.2983-8G>A | DAAM2 | ENSG00000146122.17 | transcript | ENST00000274867.9 | protein_coding | 24/24 | chr6 | 39901805 |