Item | Value |
---|---|
geneid | 7499 |
ensemblid | ENSG00000124343.14 |
hgncid | 12806 |
symbol | XG |
name | Xg glycoprotein (Xg blood group) |
refseq_nuc | NM_001141919.2 |
refseq_prot | NP_001135391.1 |
ensembl_nuc | ENST00000644266.2 |
ensembl_prot | ENSP00000494087.1 |
mane_status | MANE Select |
chr | chrX |
start | 2752040 |
end | 2816500 |
strand | + |
ver | v1.2 |
region | chrX:2752040-2816500 |
region5000 | chrX:2747040-2821500 |
regionname0 | XG_chrX_2752040_2816500 |
regionname5000 | XG_chrX_2747040_2821500 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 195 | 301 | 71 | 49 | 143 | 9 | 29 | 110 | XG_chrX_2747040_2821500 | XG | MESWW others(190): Show |
chrX | 2747040 | 2821500 |
a0002 | 1/0 | 195 | 13 | 7 | 4 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | MESWW others(190): Show |
chrX | 2747040 | 2821500 |
a0003 | 0/1 | 195 | 7 | 0 | 2 | 0 | 4 | 0 | 0 | XG_chrX_2747040_2821500 | XG | MESWW others(190): Show |
chrX | 2747040 | 2821500 |
a0004 | 0/0 | 195 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | MESWW others(190): Show |
chrX | 2747040 | 2821500 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 585 | 282 | 53 | 49 | 143 | 9 | 28 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0001c0002 | 0/0 | 585 | 16 | 16 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0001c0005 | 0/0 | 585 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0001c0006 | 0/0 | 585 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0002c0003 | 1/0 | 585 | 12 | 6 | 4 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0002c0007 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0003c0004 | 0/1 | 585 | 7 | 0 | 2 | 0 | 4 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 | ||
a0004c0008 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ATGGA others(580): Show |
chrX | 2747040 | 2821500 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2959 | 99 | 13 | 13 | 54 | 6 | 13 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0002 | 0/0 | 2957 | 37 | 0 | 18 | 13 | 3 | 3 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0003 | 0/0 | 2955 | 39 | 6 | 5 | 25 | 0 | 3 | XG_chrX_2747040_2821500 | XG | ACACG others(2950): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0004 | 0/0 | 2959 | 22 | 0 | 0 | 22 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0005 | 0/0 | 2953 | 14 | 11 | 2 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0006 | 0/0 | 2953 | 12 | 0 | 1 | 10 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0007 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2936): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0008 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0009 | 0/0 | 2961 | 3 | 0 | 1 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2956): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0010 | 0/0 | 2955 | 4 | 2 | 1 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ACACG others(2950): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0011 | 0/0 | 2947 | 4 | 0 | 3 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ACACG others(2942): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0012 | 0/0 | 2945 | 2 | 1 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2940): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0013 | 0/0 | 2957 | 3 | 3 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0014 | 0/0 | 2955 | 3 | 0 | 0 | 0 | 0 | 3 | XG_chrX_2747040_2821500 | XG | ACACG others(2950): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0015 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0016 | 0/0 | 2955 | 3 | 0 | 0 | 1 | 0 | 2 | XG_chrX_2747040_2821500 | XG | ACACG others(2950): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0017 | 0/0 | 2949 | 3 | 0 | 0 | 3 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2944): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0018 | 0/0 | 2949 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACA others(2944): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0019 | 0/0 | 2957 | 2 | 1 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0020 | 0/0 | 2953 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0021 | 0/0 | 2955 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2950): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0022 | 0/0 | 2941 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2936): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0023 | 0/0 | 2963 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2958): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0024 | 0/0 | 2959 | 2 | 0 | 0 | 1 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0025 | 0/0 | 2953 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0027 | 0/0 | 2959 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0028 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0029 | 0/0 | 2953 | 2 | 0 | 0 | 2 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0030 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0033 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0036 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0038 | 0/0 | 2961 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2956): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0039 | 0/0 | 2959 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0041 | 0/0 | 2965 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2960): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0043 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0044 | 0/0 | 2953 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0045 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2940): Show |
chrX | 2747040 | 2821500 |
a0001c0001t0046 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0001 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0005 | 0/0 | 2953 | 4 | 4 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0007 | 0/0 | 2941 | 5 | 5 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2936): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0008 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0012 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2940): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0034 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0040 | 0/0 | 2953 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2948): Show |
chrX | 2747040 | 2821500 |
a0001c0002t0042 | 0/0 | 2945 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2940): Show |
chrX | 2747040 | 2821500 |
a0001c0005t0015 | 0/0 | 2957 | 2 | 2 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0001c0006t0032 | 0/0 | 2943 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0001 | 0/0 | 2959 | 3 | 2 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0007 | 0/0 | 2941 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2936): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0008 | 0/0 | 2943 | 4 | 3 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0026 | 0/0 | 2959 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0028 | 1/0 | 2943 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2938): Show |
chrX | 2747040 | 2821500 |
a0002c0003t0031 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2958): Show |
chrX | 2747040 | 2821500 |
a0002c0007t0037 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2958): Show |
chrX | 2747040 | 2821500 |
a0003c0004t0001 | 0/0 | 2959 | 2 | 0 | 1 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
a0003c0004t0002 | 0/1 | 2957 | 3 | 0 | 1 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2952): Show |
chrX | 2747040 | 2821500 |
a0003c0004t0009 | 0/0 | 2961 | 2 | 0 | 0 | 0 | 2 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2956): Show |
chrX | 2747040 | 2821500 |
a0004c0008t0035 | 0/0 | 2959 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | ACACG others(2954): Show |
chrX | 2747040 | 2821500 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0010g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0011g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0011g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0011g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0012g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0014g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0014g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0015g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0016g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0016g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0017g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0017g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0017g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0018g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0019g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0020g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0020g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0021g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0021g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0023g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0023g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0024g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0024g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0025g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0027g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0027g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0028g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0029g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0029g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0030g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0033g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0036g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0038g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0039g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0041g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0043g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0044g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0045g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0001t0046g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0040g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0002t0042g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0005t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0005t0015g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0001c0006t0032g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0026g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0026g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0028g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0003t0031g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0002c0007t0037g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0002g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0009g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0003c0004t0009g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
a0004c0008t0035g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0002 | g0210 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00140 | hp1 | a0003 | c0004 | t0001 | g0227 | EUR | GBR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00438 | hp2 | a0001 | c0001 | t0029 | g0279 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00558 | hp2 | a0001 | c0001 | t0017 | g0042 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00597 | hp1 | a0001 | c0001 | t0019 | g0242 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00621 | hp1 | a0001 | c0001 | t0029 | g0128 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0202 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00741 | hp1 | a0002 | c0003 | t0031 | g0110 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0218 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01070 | hp2 | a0001 | c0001 | t0023 | g0006 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01071 | hp1 | a0001 | c0001 | t0023 | g0004 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01074 | hp1 | a0001 | c0001 | t0044 | g0124 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0286 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01167 | hp1 | a0002 | c0003 | t0026 | g0310 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01168 | hp1 | a0003 | c0004 | t0002 | g0056 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01169 | hp1 | a0002 | c0003 | t0026 | g0311 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01175 | hp1 | a0001 | c0001 | t0011 | g0243 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0247 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01243 | hp2 | a0002 | c0003 | t0008 | g0013 | AMR | PUR | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01257 | hp1 | a0001 | c0001 | t0038 | g0151 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0207 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01361 | hp2 | a0003 | c0004 | t0001 | g0228 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01515 | hp2 | a0003 | c0004 | t0009 | g0301 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0313 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01517 | hp2 | a0003 | c0004 | t0009 | g0292 | EUR | IBS | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0309 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0302 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0289 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0073 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02135 | hp1 | a0001 | c0001 | t0017 | g0269 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02145 | hp1 | a0001 | c0002 | t0007 | g0188 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02155 | hp1 | a0001 | c0001 | t0030 | g0057 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02257 | hp1 | a0001 | c0001 | t0010 | g0174 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0136 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02280 | hp1 | a0001 | c0001 | t0041 | g0190 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02451 | hp1 | a0001 | c0002 | t0007 | g0308 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02523 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | KHV | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02572 | hp2 | a0001 | c0001 | t0020 | g0147 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02602 | hp1 | a0001 | c0001 | t0010 | g0048 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02615 | hp1 | a0002 | c0003 | t0007 | g0009 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02622 | hp1 | a0001 | c0001 | t0021 | g0278 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02647 | hp2 | a0001 | c0002 | t0012 | g0047 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02717 | hp2 | a0001 | c0002 | t0034 | g0010 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02723 | hp2 | a0001 | c0001 | t0022 | g0005 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0149 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02809 | hp1 | a0001 | c0002 | t0007 | g0007 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02809 | hp2 | a0001 | c0005 | t0015 | g0043 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0050 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0307 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02897 | hp1 | a0001 | c0001 | t0013 | g0303 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02922 | hp2 | a0004 | c0008 | t0035 | g0282 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02970 | hp1 | a0001 | c0001 | t0021 | g0020 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0032 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02976 | hp1 | a0002 | c0003 | t0008 | g0065 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02976 | hp2 | a0001 | c0001 | t0043 | g0123 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03017 | hp1 | a0001 | c0001 | t0014 | g0095 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0192 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0008 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03139 | hp1 | a0001 | c0005 | t0015 | g0049 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03195 | hp2 | a0001 | c0001 | t0045 | g0121 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03209 | hp1 | a0001 | c0001 | t0036 | g0002 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03225 | hp2 | a0001 | c0001 | t0025 | g0027 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03239 | hp1 | a0001 | c0001 | t0016 | g0277 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03453 | hp2 | a0001 | c0002 | t0040 | g0135 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03486 | hp2 | a0002 | c0007 | t0037 | g0097 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03491 | hp1 | a0001 | c0001 | t0014 | g0206 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0186 | AFR | ESN | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03710 | hp1 | a0001 | c0006 | t0032 | g0100 | SAS | PJL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03831 | hp2 | a0001 | c0001 | t0014 | g0258 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03834 | hp2 | a0001 | c0001 | t0016 | g0233 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | STU | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18522 | hp2 | a0001 | c0001 | t0028 | g0026 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18906 | hp2 | a0002 | c0003 | t0008 | g0064 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18941 | hp1 | a0001 | c0001 | t0016 | g0293 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18950 | hp1 | a0001 | c0001 | t0027 | g0167 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18964 | hp2 | a0001 | c0001 | t0027 | g0209 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18967 | hp2 | a0001 | c0001 | t0009 | g0103 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18973 | hp2 | a0001 | c0001 | t0039 | g0034 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18975 | hp1 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18993 | hp2 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18994 | hp1 | a0001 | c0001 | t0018 | g0198 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19000 | hp1 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0276 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0275 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19077 | hp1 | a0001 | c0001 | t0033 | g0268 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19080 | hp2 | a0001 | c0001 | t0024 | g0087 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19081 | hp1 | a0001 | c0001 | t0015 | g0164 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19083 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19085 | hp2 | a0001 | c0001 | t0017 | g0270 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA19240 | hp2 | a0001 | c0001 | t0046 | g0122 | AFR | YRI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ASW | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20129 | hp2 | a0001 | c0001 | t0022 | g0189 | AFR | ASW | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0314 | EUR | TSI | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20905 | hp2 | a0001 | c0001 | t0024 | g0182 | SAS | GIH | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0126 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02109 | hp2 | a0001 | c0001 | t0020 | g0132 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02486 | hp1 | a0001 | c0002 | t0008 | g0321 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG06807 | hp1 | a0002 | c0003 | t0008 | g0125 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
HG06807 | hp2 | a0001 | c0002 | t0042 | g0033 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA18955 | hp2 | a0001 | c0001 | t0018 | g0199 | EAS | JPT | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20300 | hp1 | a0001 | c0002 | t0005 | g0285 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA20300 | hp2 | a0001 | c0001 | t0025 | g0317 | AFR | USA | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | LWK | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
homoSapiens | chm13v2 | a0003 | c0004 | t0002 | g0236 | REF | REF | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
homoSapiens | grch38p0 | a0002 | c0003 | t0028 | g0249 | REF | REF | XG_chrX_2747040_2821500 | XG | chrX | 2747040 | 2821500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2782116 | G | A | 1 | a0003 | 6 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(3): Show |
missense_variant | MODERATE | c.178G>A | p.Asp60Asn | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/11 | 413/2943 | 178/588 | 60/195 | chrX | 2782116 | |||
chrX:2789667 | C | T | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.214C>T | p.Arg72Cys | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/11 | 449/2943 | 214/588 | 72/195 | chrX | 2789667 | |||
chrX:2806719 | T | C | 3 | a0001 a0003 a0004 |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
missense_variant | MODERATE | c.392T>C | p.Leu131Pro | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/11 | 627/2943 | 392/588 | 131/195 | chrX | 2806719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2789693 | C | T | 2 | a0001c0002 a0002c0007 |
17 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
synonymous_variant | LOW | c.240C>T | p.Ser80Ser | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/11 | 475/2943 | 240/588 | 80/195 | chrX | 2789693 | |||
chrX:2808207 | T | C | 1 | a0001c0005 | 2 | HG02809.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.441T>C | p.Tyr147Tyr | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/11 | 676/2943 | 441/588 | 147/195 | chrX | 2808207 | |||
chrX:2811367 | C | A | 1 | a0001c0006 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.486C>A | p.Ile162Ile | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/11 | 721/2943 | 486/588 | 162/195 | chrX | 2811367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2752044 | G | A | 1 | a0001c0001t0018 | 2 | NA18955.hp2 NA18994.hp1 |
5_prime_UTR_variant | MODIFIER | c.-231G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 231 | chrX | 2752044 | ||||||
chrX:2752093 | G | A | 1 | a0001c0001t0030 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 182 | chrX | 2752093 | ||||||
chrX:2752241 | A | G | 4 | a0001c0001t0043 a0001c0001t0044 a0001c0001t0045 others(1): Show |
4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-34A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/11 | 34 | chrX | 2752241 | ||||||
chrX:2814593 | G | A | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0019 others(6): Show |
64 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*213G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 213 | chrX | 2814593 | ||||||
chrX:2814693 | T | C | 3 | a0001c0001t0012 a0001c0001t0045 a0001c0002t0012 |
4 | HG00733.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*313T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 313 | chrX | 2814693 | ||||||
chrX:2815068 | T | G | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(34): Show |
232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*688T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 688 | chrX | 2815068 | ||||||
chrX:2815169 | G | A | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(34): Show |
232 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*789G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 789 | chrX | 2815169 | ||||||
chrX:2815235 | G | A | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 855 | chrX | 2815235 | ||||||
chrX:2815251 | C | G | 1 | a0001c0002t0040 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 871 | chrX | 2815251 | ||||||
chrX:2815313 | G | T | 1 | a0002c0003t0026 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*933G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 933 | chrX | 2815313 | ||||||
chrX:2815429 | A | G | 1 | a0001c0001t0025 | 2 | HG03225.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1049A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1049 | chrX | 2815429 | ||||||
chrX:2815440 | G | C | 1 | a0001c0001t0020 | 2 | HG02109.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1060G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1060 | chrX | 2815440 | ||||||
chrX:2815600 | A | G | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1220A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1220 | chrX | 2815600 | ||||||
chrX:2815627 | G | A | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(37): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1247 | chrX | 2815627 | ||||||
chrX:2815743 | A | G | 1 | a0001c0001t0039 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1363A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1363 | chrX | 2815743 | ||||||
chrX:2815761 | G | A | 1 | a0002c0003t0031 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1381 | chrX | 2815761 | ||||||
chrX:2815800 | T | TAC | 4 | a0001c0001t0012 a0001c0001t0045 a0001c0002t0012 others(1): Show |
5 | HG00733.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1442dupAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACAC | 1 | a0001c0001t0011 | 4 | HG00741.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1439_*1442dupACAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACAC | 2 | a0001c0001t0017 a0001c0001t0018 |
5 | HG00558.hp2 HG02135.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1442dupACAC others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(3): Show |
10 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0020 others(7): Show |
40 | HG00438.hp2 HG00621.hp1 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1433_*1442dupACAC others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(5): Show |
4 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 others(1): Show |
47 | HG00408.hp1 HG00673.hp1 HG01975.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1431_*1442dupACAC others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(7): Show |
5 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0019 others(2): Show |
45 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1429_*1442dupACAC others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(9): Show |
2 | a0001c0001t0027 a0004c0008t0035 |
3 | HG02922.hp2 NA18950.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1427_*1442dupACAC others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(13): Show |
1 | a0002c0003t0031 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1423_*1442dupACAC others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACACACA others(15): Show |
1 | a0001c0001t0041 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421_*1442dupACAC others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACATACA others(5): Show |
1 | a0001c0001t0010 | 4 | HG01106.hp1 HG02257.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACATACA others(7): Show |
2 | a0001c0001t0015 a0001c0005t0015 |
3 | HG02809.hp2 HG03139.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACATACA others(9): Show |
10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0030 others(7): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACATACA others(11): Show |
2 | a0001c0001t0009 a0003c0004t0009 |
5 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TACATACA others(13): Show |
1 | a0001c0001t0023 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1423_*1424insTACA others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TATATACA others(9): Show |
1 | a0001c0001t0024 | 2 | NA19080.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1421_*1422insTATA others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1422 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | T | TATATACA others(11): Show |
1 | a0001c0001t0038 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421_*1422insTATA others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1422 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815800 | TAC | T | 4 | a0001c0001t0007 a0001c0001t0022 a0001c0002t0007 others(1): Show |
9 | HG02145.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1441_*1442delAC | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1441 | INFO_REALIGN_3_PRIME | chrX | 2815800 | |||||
chrX:2815804 | C | T | 1 | a0002c0007t0037 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1424C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1424 | chrX | 2815804 | ||||||
chrX:2815821 | A | ACACACAC others(13): Show |
1 | a0002c0007t0037 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442_*1443insACAC others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1443 | INFO_REALIGN_3_PRIME | chrX | 2815821 | |||||
chrX:2815821 | A | C | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(15): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1441A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1441 | chrX | 2815821 | ||||||
chrX:2815835 | A | C | 1 | a0001c0001t0004 | 22 | HG00597.hp2 HG02071.hp1 HG02129.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1455A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1455 | chrX | 2815835 | ||||||
chrX:2815968 | A | C | 1 | a0001c0001t0013 | 3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1588A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1588 | chrX | 2815968 | ||||||
chrX:2816014 | C | T | 1 | a0001c0001t0021 | 2 | HG02622.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1634C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 11/11 | 1634 | chrX | 2816014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2752405 | C | G | 1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.61+70C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752405 | |||||||
chrX:2752450 | A | G | 3 | a0001c0001t0003g0319 a0001c0001t0004g0318 a0001c0001t0004g0320 |
3 | NA18943.hp2 NA18968.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.61+115A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752450 | |||||||
chrX:2752500 | G | A | 120 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(117): Show |
120 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+165G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752500 | |||||||
chrX:2752551 | G | T | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(142): Show |
145 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.61+216G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752551 | |||||||
chrX:2752558 | G | A | 5 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(2): Show |
5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+223G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752558 | |||||||
chrX:2752584 | A | G | 1 | a0001c0001t0025g0317 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61+249A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752584 | |||||||
chrX:2752631 | A | G | 4 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0002g0313 others(1): Show |
4 | HG00642.hp1 HG01516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+296A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2752631 | |||||||
chrX:2753244 | G | T | 121 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(118): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.61+909G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753244 | |||||||
chrX:2753325 | A | G | 26 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(23): Show |
26 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.61+990A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753325 | |||||||
chrX:2753509 | A | G | 33 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(30): Show |
33 | HG01074.hp1 HG01496.hp1 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.61+1174A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753509 | |||||||
chrX:2753519 | G | A | 1 | a0002c0003t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.61+1184G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753519 | |||||||
chrX:2753594 | T | C | 5 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(2): Show |
5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1259T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753594 | |||||||
chrX:2753627 | G | C | 13 | a0001c0001t0001g0287 a0001c0001t0001g0315 a0001c0001t0001g0316 others(10): Show |
13 | HG00642.hp1 HG01106.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+1292G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753627 | |||||||
chrX:2753727 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.61+1392T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753727 | |||||||
chrX:2753762 | T | G | 1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1427T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753762 | |||||||
chrX:2753827 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+1492C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753827 | |||||||
chrX:2753871 | C | T | 1 | a0001c0001t0003g0254 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.61+1536C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753871 | |||||||
chrX:2753912 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.61+1577G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2753912 | |||||||
chrX:2754064 | A | T | 1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1729A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754064 | |||||||
chrX:2754065 | T | G | 1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1730T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754065 | |||||||
chrX:2754066 | G | T | 1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.61+1731G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754066 | |||||||
chrX:2754153 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61+1818C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754153 | |||||||
chrX:2754174 | C | G | 40 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(37): Show |
40 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.61+1839C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754174 | |||||||
chrX:2754464 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0129 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.61+2129A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754464 | |||||||
chrX:2754506 | A | C | 5 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(2): Show |
5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2171A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754506 | |||||||
chrX:2754572 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61+2237T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754572 | |||||||
chrX:2754574 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.61+2239G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754574 | |||||||
chrX:2754651 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0129 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.61+2316G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754651 | |||||||
chrX:2754694 | T | C | 5 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(2): Show |
5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2359T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754694 | |||||||
chrX:2754833 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.61+2498G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2754833 | |||||||
chrX:2755057 | C | T | 27 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(24): Show |
27 | HG00642.hp1 HG00738.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+2722C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755057 | |||||||
chrX:2755161 | C | T | 5 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(2): Show |
5 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2826C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755161 | |||||||
chrX:2755162 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | HG01516.hp2 HG03540.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.61+2827G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755162 | |||||||
chrX:2755338 | T | A | 1 | a0001c0001t0003g0319 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.61+3003T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755338 | |||||||
chrX:2755419 | C | T | 1 | a0001c0001t0021g0278 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61+3084C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755419 | |||||||
chrX:2755449 | T | TG | 18 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
18 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+3116dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2755449 | ||||||
chrX:2755522 | G | A | 21 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(18): Show |
21 | HG01496.hp1 HG01981.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.61+3187G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755522 | |||||||
chrX:2755526 | T | C | 4 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(1): Show |
4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3191T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755526 | |||||||
chrX:2755594 | C | A | 1 | a0001c0001t0012g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61+3259C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755594 | |||||||
chrX:2755696 | G | A | 1 | a0001c0001t0029g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.61+3361G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755696 | |||||||
chrX:2755881 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0119 others(162): Show |
166 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.61+3546T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2755881 | |||||||
chrX:2756098 | G | A | 4 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(1): Show |
4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3763G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756098 | |||||||
chrX:2756235 | C | T | 37 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(34): Show |
37 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.61+3900C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756235 | |||||||
chrX:2756249 | A | G | 1 | a0001c0002t0005g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+3914A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756249 | |||||||
chrX:2756364 | G | T | 3 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 |
3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.61+4029G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756364 | |||||||
chrX:2756373 | A | T | 1 | a0001c0001t0005g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.61+4038A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756373 | |||||||
chrX:2756593 | ATAAAT | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0119 a0001c0001t0001g0129 others(83): Show |
87 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+4263_61+4267del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2756593 | ||||||
chrX:2756701 | C | T | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+4366C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756701 | |||||||
chrX:2756706 | G | A | 1 | a0001c0001t0006g0016 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61+4371G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756706 | |||||||
chrX:2756706 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(166): Show |
170 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.61+4371G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756706 | |||||||
chrX:2756709 | C | G | 4 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(1): Show |
4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+4374C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756709 | |||||||
chrX:2756801 | G | A | 4 | a0001c0001t0043g0123 a0001c0001t0044g0124 a0001c0001t0045g0121 others(1): Show |
4 | HG01074.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+4466G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756801 | |||||||
chrX:2756910 | G | A | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.61+4575G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2756910 | |||||||
chrX:2757065 | C | T | 1 | a0001c0001t0004g0117 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.61+4730C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757065 | |||||||
chrX:2757421 | G | C | 193 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(190): Show |
193 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.61+5086G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757421 | |||||||
chrX:2757449 | G | A | 3 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 |
3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.61+5114G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757449 | |||||||
chrX:2757475 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.61+5140G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757475 | |||||||
chrX:2757566 | CTGAGTAC others(7): Show |
C | 1 | a0001c0001t0001g0022 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.61+5238_61+5251del others(14): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757566 | ||||||
chrX:2757740 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0003g0024 |
2 | NA18971.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.61+5405G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757740 | |||||||
chrX:2757797 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0113 a0001c0001t0001g0115 others(3): Show |
6 | HG02523.hp2 NA18981.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+5462C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2757797 | |||||||
chrX:2757971 | C | CA | 19 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0134 others(16): Show |
19 | HG00741.hp2 HG01257.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+5661dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2757971 | CA | C | 37 | a0001c0001t0001g0252 a0001c0001t0001g0261 a0001c0001t0001g0262 others(34): Show |
37 | HG01074.hp1 HG01109.hp2 HG01993.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+5661delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2757971 | CAAAAAA | C | 13 | a0001c0001t0001g0195 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.61+5656_61+5661del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2757971 | CAAAAAAA | C | 104 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(101): Show |
104 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.61+5655_61+5661del others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2757971 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61+5650_61+5661del others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2757971 | CAAAAAAA others(6): Show |
C | 29 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0304 others(26): Show |
29 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.61+5649_61+5661del others(13): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2757971 | ||||||
chrX:2758018 | C | T | 8 | a0001c0001t0003g0283 a0001c0001t0005g0003 a0001c0001t0005g0284 others(5): Show |
8 | HG01106.hp1 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+5683C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758018 | |||||||
chrX:2758042 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0001g0264 a0001c0001t0001g0265 others(10): Show |
13 | HG02004.hp2 HG02135.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+5707C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758042 | |||||||
chrX:2758044 | C | G | 13 | a0001c0001t0001g0259 a0001c0001t0001g0264 a0001c0001t0001g0265 others(10): Show |
13 | HG02004.hp2 HG02135.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+5709C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758044 | |||||||
chrX:2758119 | T | C | 190 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(187): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.61+5784T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758119 | |||||||
chrX:2758395 | C | G | 2 | a0001c0001t0002g0248 a0001c0001t0038g0151 |
2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.61+6060C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758395 | |||||||
chrX:2758408 | A | G | 1 | a0001c0001t0005g0140 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.61+6073A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758408 | |||||||
chrX:2758411 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.61+6076C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758411 | |||||||
chrX:2758446 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.61+6111C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758446 | |||||||
chrX:2758457 | G | A | 3 | a0001c0001t0002g0109 a0001c0001t0003g0319 a0001c0001t0004g0191 |
3 | HG02155.hp2 HG04115.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.61+6122G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758457 | |||||||
chrX:2758472 | C | G | 1 | a0001c0001t0004g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.61+6137C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758472 | |||||||
chrX:2758639 | G | A | 7 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0021g0020 others(4): Show |
7 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+6304G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758639 | |||||||
chrX:2758814 | G | C | 1 | a0001c0001t0043g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.61+6479G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758814 | |||||||
chrX:2758874 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.61+6539C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758874 | |||||||
chrX:2758881 | C | A | 1 | a0001c0001t0002g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61+6546C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758881 | |||||||
chrX:2758944 | T | C | 10 | a0001c0001t0001g0129 a0001c0001t0003g0045 a0001c0001t0003g0046 others(7): Show |
10 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+6609T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758944 | |||||||
chrX:2758952 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0208 |
3 | HG01168.hp2 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.61+6617C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758952 | |||||||
chrX:2758956 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0138 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+6621T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2758956 | |||||||
chrX:2758956 | T | TTATC | 233 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.61+6627_61+6630dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2758956 | ||||||
chrX:2759032 | GTATC | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6706_61+6709del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759032 | ||||||
chrX:2759050 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6715G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759050 | |||||||
chrX:2759060 | C | G | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0004g0117 others(1): Show |
4 | NA18963.hp1 NA18967.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+6725C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759060 | |||||||
chrX:2759093 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6758G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759093 | |||||||
chrX:2759094 | T | C | 10 | a0001c0001t0001g0213 a0001c0001t0001g0250 a0001c0001t0010g0048 others(7): Show |
10 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+6759T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759094 | |||||||
chrX:2759112 | C | T | 1 | a0001c0001t0010g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61+6777C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759112 | |||||||
chrX:2759113 | A | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6778A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759113 | |||||||
chrX:2759121 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.61+6786T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759121 | |||||||
chrX:2759132 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(214): Show |
218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.61+6797G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759132 | |||||||
chrX:2759317 | A | G | 37 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0212 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.61+6982A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759317 | |||||||
chrX:2759369 | C | T | 1 | a0001c0006t0032g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.61+7034C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759369 | |||||||
chrX:2759370 | G | A | 53 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0137 others(50): Show |
53 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.61+7035G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759370 | |||||||
chrX:2759375 | A | AGGAGGTA others(9): Show |
1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+7072_61+7087dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759375 | ||||||
chrX:2759375 | AGGAGGTA others(9): Show |
A | 1 | a0002c0003t0031g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61+7072_61+7087del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759375 | ||||||
chrX:2759443 | G | A | 11 | a0001c0001t0001g0304 a0001c0001t0005g0288 a0001c0001t0005g0305 others(8): Show |
11 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+7108G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759443 | |||||||
chrX:2759506 | C | T | 74 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(71): Show |
74 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.61+7171C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759506 | |||||||
chrX:2759548 | G | A | 19 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0129 others(16): Show |
19 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.61+7213G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759548 | |||||||
chrX:2759656 | G | C | 7 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0021g0020 others(4): Show |
7 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+7321G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759656 | |||||||
chrX:2759704 | A | G | 18 | a0001c0001t0001g0129 a0001c0001t0003g0045 a0001c0001t0003g0046 others(15): Show |
18 | HG01243.hp2 HG02451.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+7369A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759704 | |||||||
chrX:2759809 | C | T | 80 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.61+7474C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759809 | |||||||
chrX:2759815 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0195 others(7): Show |
10 | HG00423.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+7480C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759815 | |||||||
chrX:2759816 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0155 a0001c0001t0002g0157 others(3): Show |
6 | HG00597.hp2 HG00621.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+7481G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759816 | |||||||
chrX:2759819 | A | T | 55 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0129 others(52): Show |
55 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.61+7484A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759819 | |||||||
chrX:2759856 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0004g0051 |
2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.61+7521G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2759856 | |||||||
chrX:2759955 | T | TCTGCATG others(4): Show |
139 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0036 others(136): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.61+7621_61+7622ins others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2759955 | ||||||
chrX:2760019 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0003g0037 |
2 | HG00673.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.61+7684C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760019 | |||||||
chrX:2760034 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.61+7699C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760034 | |||||||
chrX:2760082 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.61+7747C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760082 | |||||||
chrX:2760124 | G | A | 14 | a0001c0001t0001g0250 a0001c0001t0002g0148 a0001c0001t0005g0288 others(11): Show |
14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+7789G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760124 | |||||||
chrX:2760181 | GA | G | 8 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0005g0029 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.61+7856delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760181 | ||||||
chrX:2760192 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0002g0038 |
2 | HG02027.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.61+7857T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760192 | |||||||
chrX:2760370 | T | C | 1 | a0001c0001t0006g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.61+8035T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760370 | |||||||
chrX:2760523 | CAGG | C | 5 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0021g0020 others(2): Show |
5 | HG01109.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+8191_61+8193del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760523 | ||||||
chrX:2760562 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61+8227C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760562 | |||||||
chrX:2760579 | C | CA | 61 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0036 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.61+8260dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760579 | ||||||
chrX:2760579 | CA | C | 39 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0129 others(36): Show |
39 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.61+8260delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760579 | ||||||
chrX:2760581 | A | C | 25 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0250 others(22): Show |
25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.61+8246A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760581 | |||||||
chrX:2760582 | A | C | 2 | a0001c0001t0002g0148 a0001c0001t0011g0149 |
2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.61+8247A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760582 | |||||||
chrX:2760583 | A | C | 25 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0250 others(22): Show |
25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.61+8248A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760583 | |||||||
chrX:2760584 | A | C | 2 | a0001c0001t0002g0148 a0001c0001t0011g0149 |
2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.61+8249A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760584 | |||||||
chrX:2760585 | A | C | 14 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0003g0133 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.61+8250A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760585 | |||||||
chrX:2760734 | CA | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(199): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.61+8421delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | ||||||
chrX:2760734 | CAA | C | 31 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0137 others(28): Show |
31 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.61+8420_61+8421del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | ||||||
chrX:2760734 | CAAA | C | 26 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0104 others(23): Show |
26 | HG00323.hp1 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.61+8419_61+8421del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2760734 | ||||||
chrX:2760816 | C | A | 3 | a0001c0002t0001g0011 a0001c0002t0034g0010 a0002c0003t0001g0028 |
3 | HG02451.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.61+8481C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2760816 | |||||||
chrX:2761052 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(182): Show |
186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.61+8717T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761052 | |||||||
chrX:2761465 | G | A | 11 | a0001c0001t0001g0137 a0001c0001t0003g0133 a0001c0001t0005g0029 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-9085G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761465 | |||||||
chrX:2761469 | T | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0109 others(2): Show |
5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-9081T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761469 | |||||||
chrX:2761590 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.62-8960C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761590 | |||||||
chrX:2761758 | G | A | 32 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0129 others(29): Show |
32 | HG01109.hp2 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-8792G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761758 | |||||||
chrX:2761846 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.62-8704T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761846 | |||||||
chrX:2761888 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0109 others(2): Show |
5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-8662G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761888 | |||||||
chrX:2761895 | A | G | 1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-8655A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761895 | |||||||
chrX:2761908 | G | T | 54 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0104 others(51): Show |
54 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.62-8642G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2761908 | |||||||
chrX:2762116 | G | A | 54 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0104 others(51): Show |
54 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.62-8434G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762116 | |||||||
chrX:2762144 | C | T | 55 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0104 others(52): Show |
55 | HG00323.hp1 HG00423.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.62-8406C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762144 | |||||||
chrX:2762146 | G | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0109 others(2): Show |
5 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-8404G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762146 | |||||||
chrX:2762258 | T | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.62-8292T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762258 | |||||||
chrX:2762304 | C | T | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-8246C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762304 | |||||||
chrX:2762337 | A | G | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62-8213A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762337 | |||||||
chrX:2762414 | C | T | 3 | a0001c0001t0025g0027 a0001c0001t0046g0122 a0001c0002t0008g0321 |
3 | HG02486.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.62-8136C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762414 | |||||||
chrX:2762428 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.62-8122G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762428 | |||||||
chrX:2762646 | A | T | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7904A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762646 | |||||||
chrX:2762648 | T | G | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7902T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762648 | |||||||
chrX:2762657 | G | C | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7893G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762657 | |||||||
chrX:2762730 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.62-7820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762730 | |||||||
chrX:2762731 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0002g0109 others(1): Show |
4 | HG04115.hp1 NA18946.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-7819C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762731 | |||||||
chrX:2762796 | G | T | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7754G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762796 | |||||||
chrX:2762797 | T | G | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7753T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762797 | |||||||
chrX:2762850 | A | G | 1 | a0001c0001t0003g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.62-7700A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2762850 | |||||||
chrX:2763161 | T | C | 1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-7389T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763161 | |||||||
chrX:2763165 | C | CACCA | 39 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(36): Show |
39 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-7384_62-7381dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2763165 | ||||||
chrX:2763174 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.62-7376G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763174 | |||||||
chrX:2763290 | G | A | 11 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0181 others(8): Show |
11 | HG00280.hp1 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-7260G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763290 | |||||||
chrX:2763470 | C | A | 1 | a0001c0001t0027g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.62-7080C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763470 | |||||||
chrX:2763471 | A | G | 271 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(268): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.62-7079A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763471 | |||||||
chrX:2763510 | C | G | 267 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(264): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.62-7040C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763510 | |||||||
chrX:2763775 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-6775A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763775 | |||||||
chrX:2763790 | T | A | 23 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0130 others(20): Show |
23 | HG00323.hp1 HG00423.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-6760T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763790 | |||||||
chrX:2763829 | A | G | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-6721A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763829 | |||||||
chrX:2763831 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62-6719G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763831 | |||||||
chrX:2763837 | A | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
25 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.62-6713A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763837 | |||||||
chrX:2763848 | G | T | 1 | a0001c0006t0032g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.62-6702G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763848 | |||||||
chrX:2763891 | T | G | 231 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(228): Show |
231 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.62-6659T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763891 | |||||||
chrX:2763925 | G | C | 59 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.62-6625G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763925 | |||||||
chrX:2763977 | G | A | 260 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(257): Show |
260 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.62-6573G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2763977 | |||||||
chrX:2764108 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(309): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.62-6442T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764108 | |||||||
chrX:2764120 | C | T | 2 | a0001c0001t0003g0283 a0001c0001t0043g0123 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.62-6430C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764120 | |||||||
chrX:2764135 | T | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(310): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.62-6415T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764135 | |||||||
chrX:2764172 | C | T | 2 | a0001c0001t0001g0137 a0001c0002t0042g0033 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-6378C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764172 | |||||||
chrX:2764175 | C | T | 2 | a0001c0001t0001g0137 a0001c0002t0042g0033 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-6375C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764175 | |||||||
chrX:2764227 | G | A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0213 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-6323G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764227 | |||||||
chrX:2764349 | C | A | 1 | a0002c0003t0008g0013 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-6201C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764349 | |||||||
chrX:2764367 | G | A | 1 | a0001c0001t0014g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-6183G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764367 | |||||||
chrX:2764369 | C | G | 1 | a0001c0001t0014g0258 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.62-6181C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764369 | |||||||
chrX:2764377 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.62-6173C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764377 | |||||||
chrX:2764654 | C | A | 1 | a0001c0001t0006g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.62-5896C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764654 | |||||||
chrX:2764700 | T | C | 2 | a0001c0001t0001g0137 a0001c0002t0042g0033 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-5850T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764700 | |||||||
chrX:2764778 | T | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.62-5772T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764778 | |||||||
chrX:2764814 | G | T | 7 | a0001c0001t0003g0283 a0001c0001t0005g0003 a0001c0001t0005g0019 others(4): Show |
7 | HG01261.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-5736G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764814 | |||||||
chrX:2764873 | A | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(40): Show |
43 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-5677A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764873 | |||||||
chrX:2764874 | T | C | 43 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(40): Show |
43 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.62-5676T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764874 | |||||||
chrX:2764884 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.62-5666C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764884 | |||||||
chrX:2764906 | T | G | 3 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 |
3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-5644T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764906 | |||||||
chrX:2764989 | C | T | 19 | a0001c0001t0001g0092 a0001c0001t0002g0109 a0001c0001t0003g0283 others(16): Show |
19 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-5561C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2764989 | |||||||
chrX:2765011 | A | C | 2 | a0001c0001t0004g0246 a0001c0001t0006g0061 |
2 | NA19002.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.62-5539A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765011 | |||||||
chrX:2765041 | C | CA | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(199): Show |
203 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.62-5485dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | ||||||
chrX:2765041 | C | CAA | 53 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0067 others(50): Show |
53 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.62-5486_62-5485dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | ||||||
chrX:2765041 | C | CAAA | 11 | a0001c0001t0001g0092 a0001c0001t0001g0168 a0001c0001t0003g0045 others(8): Show |
11 | HG02572.hp2 HG02809.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-5487_62-5485dup others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | ||||||
chrX:2765041 | CAAAAAA | C | 6 | a0001c0001t0003g0012 a0001c0001t0003g0201 a0001c0001t0005g0288 others(3): Show |
6 | HG00558.hp2 HG01891.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-5490_62-5485del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765041 | ||||||
chrX:2765057 | A | AG | 26 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0116 others(23): Show |
26 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.62-5493_62-5492ins others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765057 | |||||||
chrX:2765057 | A | G | 1 | a0001c0001t0027g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.62-5493A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765057 | |||||||
chrX:2765124 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(60): Show |
64 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.62-5426G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765124 | |||||||
chrX:2765125 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-5425A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765125 | |||||||
chrX:2765152 | C | G | 268 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(265): Show |
268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.62-5398C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765152 | |||||||
chrX:2765156 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0009g0103 |
2 | NA18967.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.62-5394G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765156 | |||||||
chrX:2765185 | A | C | 54 | a0001c0001t0001g0022 a0001c0001t0001g0085 a0001c0001t0001g0086 others(51): Show |
54 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.62-5365A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765185 | |||||||
chrX:2765189 | TA | T | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0084 others(3): Show |
6 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5353delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765189 | ||||||
chrX:2765191 | A | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0107 others(29): Show |
32 | HG00741.hp1 HG01074.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.62-5359A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765191 | |||||||
chrX:2765192 | A | C | 5 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0005g0044 others(2): Show |
5 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5358A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765192 | |||||||
chrX:2765195 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.62-5355A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765195 | |||||||
chrX:2765200 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(257): Show |
261 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.62-5350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765200 | |||||||
chrX:2765220 | G | A | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0134 others(42): Show |
45 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.62-5330G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765220 | |||||||
chrX:2765257 | G | A | 235 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(232): Show |
235 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.62-5293G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765257 | |||||||
chrX:2765278 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62-5272G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765278 | |||||||
chrX:2765283 | A | G | 82 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.62-5267A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765283 | |||||||
chrX:2765365 | A | G | 5 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0019g0186 others(2): Show |
5 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5185A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765365 | |||||||
chrX:2765372 | GGGAGGGA others(5): Show |
G | 5 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0019g0186 others(2): Show |
5 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-5174_62-5163del others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765372 | ||||||
chrX:2765376 | G | GGGAA | 29 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0134 others(26): Show |
29 | HG00423.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.62-5137_62-5134dup others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(1): Show |
40 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(37): Show |
40 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.62-5141_62-5134dup others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(5): Show |
6 | a0001c0001t0002g0109 a0001c0001t0003g0099 a0001c0001t0003g0251 others(3): Show |
6 | HG00408.hp1 HG02970.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5145_62-5134dup others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(9): Show |
4 | a0001c0001t0003g0045 a0001c0001t0003g0093 a0001c0001t0013g0309 others(1): Show |
4 | HG01884.hp1 HG04204.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-5149_62-5134dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(13): Show |
6 | a0001c0001t0003g0046 a0001c0001t0005g0044 a0001c0001t0005g0288 others(3): Show |
6 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-5153_62-5134dup others(20): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(17): Show |
6 | a0001c0001t0002g0148 a0001c0001t0003g0283 a0001c0001t0010g0174 others(3): Show |
6 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-5157_62-5134dup others(24): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(21): Show |
2 | a0001c0001t0001g0250 a0001c0001t0010g0048 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.62-5161_62-5134dup others(28): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | G | GGGAAGGA others(25): Show |
1 | a0001c0001t0011g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-5165_62-5134dup others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | GGGAA | G | 11 | a0001c0001t0001g0137 a0001c0001t0001g0181 a0001c0001t0002g0145 others(8): Show |
11 | HG01099.hp1 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-5137_62-5134del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765376 | GGGAAGGA others(1): Show |
G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0052 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.62-5141_62-5134del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765376 | ||||||
chrX:2765401 | G | GGAAGGAA others(4): Show |
1 | a0001c0001t0004g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.62-5147_62-5137dup others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765401 | ||||||
chrX:2765452 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0273 |
3 | HG01516.hp1 HG01517.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.62-5098C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765452 | |||||||
chrX:2765491 | G | C | 2 | a0001c0001t0001g0137 a0001c0002t0042g0033 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-5059G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765491 | |||||||
chrX:2765518 | T | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0134 others(16): Show |
19 | HG00741.hp1 HG01074.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-5032T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765518 | |||||||
chrX:2765541 | T | C | 4 | a0001c0001t0013g0309 a0001c0001t0021g0278 a0001c0002t0007g0050 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-5009T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765541 | |||||||
chrX:2765616 | C | T | 1 | a0001c0001t0016g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-4934C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765616 | |||||||
chrX:2765755 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-4795T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765755 | |||||||
chrX:2765769 | A | G | 147 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(144): Show |
147 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.62-4781A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765769 | |||||||
chrX:2765796 | C | CATT | 24 | a0001c0001t0001g0092 a0001c0001t0001g0250 a0001c0001t0002g0148 others(21): Show |
24 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.62-4747_62-4745dup others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2765796 | ||||||
chrX:2765867 | T | A | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-4683T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765867 | |||||||
chrX:2765868 | C | T | 1 | a0001c0001t0024g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-4682C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2765868 | |||||||
chrX:2766150 | C | CT | 37 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0195 others(34): Show |
37 | HG00323.hp1 HG00423.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.62-4391dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766150 | ||||||
chrX:2766176 | C | G | 91 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(88): Show |
91 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.62-4374C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766176 | |||||||
chrX:2766222 | T | C | 2 | a0001c0001t0004g0091 a0001c0001t0017g0269 |
2 | HG02135.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.62-4328T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766222 | |||||||
chrX:2766278 | T | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-4272T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766278 | |||||||
chrX:2766287 | C | T | 89 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.62-4263C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766287 | |||||||
chrX:2766288 | G | A | 1 | a0001c0001t0003g0254 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.62-4262G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766288 | |||||||
chrX:2766382 | G | A | 5 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0005g0044 others(2): Show |
5 | HG02572.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-4168G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766382 | |||||||
chrX:2766503 | TG | T | 190 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(187): Show |
190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.62-4041delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766503 | ||||||
chrX:2766551 | T | A | 2 | a0001c0001t0006g0255 a0001c0001t0016g0293 |
2 | NA18941.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.62-3999T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766551 | |||||||
chrX:2766557 | C | CT | 13 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0115 others(10): Show |
13 | HG01106.hp1 HG02074.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.62-3969dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766557 | CT | C | 12 | a0001c0001t0001g0101 a0001c0001t0001g0234 a0001c0001t0001g0250 others(9): Show |
12 | HG00140.hp1 HG00741.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3969delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766557 | CTTT | C | 8 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0005g0044 others(5): Show |
8 | HG00741.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-3971_62-3969del others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766557 | CTTTT | C | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0092 others(74): Show |
77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.62-3972_62-3969del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766557 | CTTTTT | C | 124 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(121): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.62-3973_62-3969del others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766557 | CTTTTTTT others(4): Show |
C | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-3979_62-3969del others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2766557 | ||||||
chrX:2766604 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3946A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766604 | |||||||
chrX:2766617 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3933T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766617 | |||||||
chrX:2766619 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3931T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766619 | |||||||
chrX:2766620 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.62-3930A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766620 | |||||||
chrX:2766621 | C | G | 8 | a0001c0001t0001g0215 a0001c0001t0001g0250 a0001c0001t0002g0148 others(5): Show |
8 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-3929C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766621 | |||||||
chrX:2766630 | A | T | 6 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0304 others(3): Show |
6 | HG00423.hp2 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3920A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766630 | |||||||
chrX:2766658 | G | A | 205 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(202): Show |
205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.62-3892G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766658 | |||||||
chrX:2766712 | C | G | 1 | a0001c0001t0009g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.62-3838C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766712 | |||||||
chrX:2766713 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.62-3837C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766713 | |||||||
chrX:2766714 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0304 a0001c0001t0003g0237 others(12): Show |
15 | HG00741.hp1 HG01074.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-3836G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766714 | |||||||
chrX:2766722 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.62-3828A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766722 | |||||||
chrX:2766725 | C | T | 15 | a0001c0001t0001g0213 a0001c0001t0001g0250 a0001c0001t0002g0148 others(12): Show |
15 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-3825C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766725 | |||||||
chrX:2766748 | C | G | 226 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(223): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.62-3802C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766748 | |||||||
chrX:2766756 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.62-3794G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766756 | |||||||
chrX:2766782 | G | A | 1 | a0001c0001t0006g0061 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.62-3768G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766782 | |||||||
chrX:2766801 | G | A | 11 | a0001c0001t0001g0250 a0001c0001t0002g0148 a0001c0001t0010g0048 others(8): Show |
11 | HG00140.hp1 HG00741.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-3749G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766801 | |||||||
chrX:2766811 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-3739T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766811 | |||||||
chrX:2766838 | T | G | 1 | a0001c0001t0004g0150 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.62-3712T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766838 | |||||||
chrX:2766854 | C | T | 6 | a0001c0001t0005g0003 a0001c0001t0005g0019 a0001c0001t0021g0020 others(3): Show |
6 | HG01261.hp1 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3696C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766854 | |||||||
chrX:2766861 | A | G | 6 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3689A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766861 | |||||||
chrX:2766887 | G | A | 2 | a0001c0001t0006g0255 a0001c0001t0016g0293 |
2 | NA18941.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.62-3663G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2766887 | |||||||
chrX:2767068 | AG | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(29): Show |
33 | HG00099.hp2 HG00544.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.62-3480delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2767068 | ||||||
chrX:2767094 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0134 others(9): Show |
12 | HG00741.hp1 HG01074.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3456C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767094 | |||||||
chrX:2767106 | G | A | 106 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.62-3444G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767106 | |||||||
chrX:2767152 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0134 others(9): Show |
12 | HG00741.hp1 HG01074.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.62-3398G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767152 | |||||||
chrX:2767194 | G | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0237 |
2 | NA18982.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.62-3356G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767194 | |||||||
chrX:2767213 | T | C | 213 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(210): Show |
213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.62-3337T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767213 | |||||||
chrX:2767220 | G | A | 210 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(207): Show |
210 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.62-3330G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767220 | |||||||
chrX:2767278 | T | A | 3 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 |
3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-3272T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767278 | |||||||
chrX:2767317 | A | T | 3 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 |
3 | HG01070.hp2 HG01071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.62-3233A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767317 | |||||||
chrX:2767387 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.62-3163C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767387 | |||||||
chrX:2767516 | T | C | 1 | a0001c0002t0007g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.62-3034T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767516 | |||||||
chrX:2767594 | C | G | 1 | a0001c0002t0005g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.62-2956C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767594 | |||||||
chrX:2767657 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0002g0272 |
2 | HG00323.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.62-2893G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767657 | |||||||
chrX:2767767 | G | A | 98 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0082 others(95): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.62-2783G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767767 | |||||||
chrX:2767810 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0260 others(2): Show |
5 | HG01099.hp1 HG01175.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-2740C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767810 | |||||||
chrX:2767818 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.62-2732G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767818 | |||||||
chrX:2767880 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18968.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.62-2670G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2767880 | |||||||
chrX:2768048 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.62-2502G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768048 | |||||||
chrX:2768078 | C | T | 60 | a0001c0001t0001g0086 a0001c0001t0001g0098 a0001c0001t0001g0129 others(57): Show |
60 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.62-2472C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768078 | |||||||
chrX:2768079 | C | T | 3 | a0001c0001t0007g0063 a0001c0001t0022g0189 a0002c0003t0001g0028 |
3 | HG02451.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62-2471C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768079 | |||||||
chrX:2768124 | A | G | 60 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0098 others(57): Show |
60 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.62-2426A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768124 | |||||||
chrX:2768233 | G | C | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-2317G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768233 | |||||||
chrX:2768261 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18946.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.62-2289A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768261 | |||||||
chrX:2768279 | C | T | 1 | a0001c0001t0005g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-2271C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768279 | |||||||
chrX:2768461 | C | T | 100 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.62-2089C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768461 | |||||||
chrX:2768475 | G | T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0094 others(5): Show |
8 | HG00673.hp1 NA18944.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2075G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768475 | |||||||
chrX:2768545 | G | A | 94 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0041 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.62-2005G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768545 | |||||||
chrX:2768682 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0004g0142 |
2 | NA18946.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.62-1868C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768682 | |||||||
chrX:2768732 | C | A | 1 | a0001c0002t0007g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.62-1818C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768732 | |||||||
chrX:2768825 | T | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0039 others(151): Show |
155 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.62-1725T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768825 | |||||||
chrX:2768850 | C | G | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.62-1700C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768850 | |||||||
chrX:2768858 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.62-1692C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2768858 | |||||||
chrX:2769087 | C | T | 1 | a0001c0001t0005g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.62-1463C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769087 | |||||||
chrX:2769268 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0005g0044 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-1282G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769268 | |||||||
chrX:2769281 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(213): Show |
217 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.62-1269T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769281 | |||||||
chrX:2769399 | A | T | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62-1151A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769399 | |||||||
chrX:2769517 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0039 others(153): Show |
157 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.62-1033A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769517 | |||||||
chrX:2769531 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0055 others(53): Show |
57 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.62-1019C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769531 | |||||||
chrX:2769879 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.62-671T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769879 | |||||||
chrX:2769887 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-663G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769887 | |||||||
chrX:2769919 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0005g0044 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-631A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2769919 | |||||||
chrX:2770016 | T | G | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.62-534T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770016 | |||||||
chrX:2770016 | TGGA | T | 4 | a0001c0001t0001g0094 a0001c0001t0004g0183 a0001c0001t0006g0016 others(1): Show |
4 | HG02683.hp2 HG02735.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-531_62-529delAG others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770016 | ||||||
chrX:2770017 | G | C | 3 | a0001c0001t0007g0063 a0001c0001t0022g0189 a0002c0003t0001g0028 |
3 | HG02451.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62-533G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770017 | |||||||
chrX:2770017 | GGA | G | 14 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0067 others(11): Show |
14 | HG00280.hp1 HG00673.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-531_62-530delAG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 2770017 | ||||||
chrX:2770018 | GA | G | 24 | a0001c0001t0001g0070 a0001c0001t0001g0088 a0001c0001t0001g0089 others(21): Show |
24 | HG00621.hp1 HG01192.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.62-531delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770018 | |||||||
chrX:2770019 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.62-531A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770019 | |||||||
chrX:2770019 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0265 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-531A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770019 | |||||||
chrX:2770023 | G | T | 1 | a0001c0001t0016g0277 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-527G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770023 | |||||||
chrX:2770024 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0055 others(52): Show |
56 | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-526T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770024 | |||||||
chrX:2770149 | G | C | 1 | a0002c0003t0008g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.62-401G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770149 | |||||||
chrX:2770248 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(156): Show |
160 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.62-302A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770248 | |||||||
chrX:2770410 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(163): Show |
167 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.62-140T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770410 | |||||||
chrX:2770501 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(162): Show |
166 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.62-49T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 1/10 | chrX | 2770501 | |||||||
chrX:2770825 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0055 others(51): Show |
55 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.103+234T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2770825 | |||||||
chrX:2770918 | T | C | 89 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.103+327T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2770918 | |||||||
chrX:2771005 | C | G | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.103+414C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771005 | |||||||
chrX:2771015 | T | C | 1 | a0001c0001t0009g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.103+424T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771015 | |||||||
chrX:2771015 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.103+424T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771015 | |||||||
chrX:2771109 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.103+518T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771109 | |||||||
chrX:2771201 | CACCCCGA others(74): Show |
C | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.103+645_103+725del others(81): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2771201 | ||||||
chrX:2771259 | A | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(165): Show |
169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.103+668A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771259 | |||||||
chrX:2771493 | T | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(168): Show |
172 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.103+902T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771493 | |||||||
chrX:2771534 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(175): Show |
179 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.103+943G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771534 | |||||||
chrX:2771560 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 |
3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+969G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771560 | |||||||
chrX:2771566 | G | A | 72 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(69): Show |
72 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.103+975G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771566 | |||||||
chrX:2771589 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.103+998G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771589 | |||||||
chrX:2771595 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 |
3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1004G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771595 | |||||||
chrX:2771782 | A | G | 46 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(43): Show |
46 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.103+1191A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771782 | |||||||
chrX:2771845 | A | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(176): Show |
180 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.103+1254A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771845 | |||||||
chrX:2771912 | C | T | 3 | a0001c0001t0001g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 |
3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1321C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2771912 | |||||||
chrX:2772222 | C | G | 1 | a0001c0001t0003g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.103+1631C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772222 | |||||||
chrX:2772242 | G | T | 1 | a0001c0001t0001g0261 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.103+1651G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772242 | |||||||
chrX:2772269 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(168): Show |
172 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.103+1678T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772269 | |||||||
chrX:2772360 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(65): Show |
69 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.103+1769C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772360 | |||||||
chrX:2772405 | G | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0052 a0001c0001t0001g0055 others(50): Show |
54 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.103+1814G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772405 | |||||||
chrX:2772410 | G | A | 3 | a0001c0001t0001g0304 a0001c0001t0005g0305 a0001c0001t0005g0306 |
3 | HG02258.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1819G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772410 | |||||||
chrX:2772773 | T | C | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-1943T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772773 | |||||||
chrX:2772786 | C | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0304 others(8): Show |
11 | HG02145.hp1 HG02258.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.104-1930C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772786 | |||||||
chrX:2772880 | C | A | 3 | a0001c0001t0010g0174 a0003c0004t0001g0227 a0003c0004t0001g0228 |
3 | HG00140.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.104-1836C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772880 | |||||||
chrX:2772881 | C | G | 3 | a0001c0001t0010g0174 a0003c0004t0001g0227 a0003c0004t0001g0228 |
3 | HG00140.hp1 HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.104-1835C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772881 | |||||||
chrX:2772967 | G | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0213 others(14): Show |
18 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.104-1749G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772967 | |||||||
chrX:2772971 | A | G | 1 | a0001c0001t0011g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-1745A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2772971 | |||||||
chrX:2773023 | A | C | 83 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0039 others(80): Show |
83 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.104-1693A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773023 | |||||||
chrX:2773048 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(172): Show |
176 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.104-1668G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773048 | |||||||
chrX:2773179 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104-1537G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773179 | |||||||
chrX:2773188 | A | G | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-1528A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773188 | |||||||
chrX:2773235 | G | A | 8 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0022g0189 others(5): Show |
8 | HG02451.hp2 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-1481G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773235 | |||||||
chrX:2773288 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1428A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773288 | |||||||
chrX:2773295 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1421T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773295 | |||||||
chrX:2773299 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1417G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773299 | |||||||
chrX:2773302 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1414G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773302 | |||||||
chrX:2773309 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1407A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773309 | |||||||
chrX:2773310 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1406A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773310 | |||||||
chrX:2773311 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1405G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773311 | |||||||
chrX:2773320 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1396G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773320 | |||||||
chrX:2773330 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1386A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773330 | |||||||
chrX:2773334 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1382A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773334 | |||||||
chrX:2773338 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1378A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773338 | |||||||
chrX:2773339 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1377A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773339 | |||||||
chrX:2773341 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1375T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773341 | |||||||
chrX:2773342 | A | G | 113 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.104-1374A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773342 | |||||||
chrX:2773344 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1372G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773344 | |||||||
chrX:2773350 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1366A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773350 | |||||||
chrX:2773359 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1357A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773359 | |||||||
chrX:2773360 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1356A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773360 | |||||||
chrX:2773366 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773366 | |||||||
chrX:2773369 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1347A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773369 | |||||||
chrX:2773370 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1346T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773370 | |||||||
chrX:2773371 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1345A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773371 | |||||||
chrX:2773381 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1335C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773381 | |||||||
chrX:2773405 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1311G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773405 | |||||||
chrX:2773416 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1300T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773416 | |||||||
chrX:2773417 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1299T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773417 | |||||||
chrX:2773421 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1295G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773421 | |||||||
chrX:2773424 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1292G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773424 | |||||||
chrX:2773425 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1291A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773425 | |||||||
chrX:2773426 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1290G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773426 | |||||||
chrX:2773429 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1287A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773429 | |||||||
chrX:2773435 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1281A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773435 | |||||||
chrX:2773442 | G | A | 2 | a0001c0001t0001g0158 a0002c0003t0008g0065 |
2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1274G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773442 | |||||||
chrX:2773444 | T | A | 2 | a0001c0001t0001g0158 a0002c0003t0008g0065 |
2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1272T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773444 | |||||||
chrX:2773445 | G | A | 2 | a0001c0001t0001g0158 a0002c0003t0008g0065 |
2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1271G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773445 | |||||||
chrX:2773448 | G | A | 2 | a0001c0001t0001g0158 a0002c0003t0008g0065 |
2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1268G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773448 | |||||||
chrX:2773457 | A | G | 2 | a0001c0001t0001g0158 a0002c0003t0008g0065 |
2 | HG02976.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.104-1259A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773457 | |||||||
chrX:2773458 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1258A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773458 | |||||||
chrX:2773458 | AGAAGAAG others(21): Show |
A | 1 | a0002c0003t0008g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.104-1253_104-1226d others(30): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773458 | ||||||
chrX:2773468 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1248G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773468 | |||||||
chrX:2773471 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1245A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773471 | |||||||
chrX:2773477 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1239G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773477 | |||||||
chrX:2773478 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1238A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773478 | |||||||
chrX:2773481 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1235G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773481 | |||||||
chrX:2773481 | GGGAA | G | 6 | a0001c0001t0001g0287 a0001c0001t0007g0063 a0001c0001t0022g0189 others(3): Show |
6 | HG00741.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-1219_104-1216d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773481 | ||||||
chrX:2773485 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1231A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773485 | |||||||
chrX:2773486 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1230G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773486 | |||||||
chrX:2773486 | G | GGAAGGAA others(9): Show |
3 | a0001c0001t0002g0177 a0001c0001t0004g0150 a0001c0001t0005g0019 |
3 | HG02132.hp1 HG02273.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.104-1086_104-1071d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(25): Show |
3 | a0001c0001t0001g0232 a0001c0001t0001g0298 a0001c0001t0003g0241 |
3 | HG00609.hp1 HG01433.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.104-1102_104-1071d others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(41): Show |
1 | a0001c0001t0002g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.104-1118_104-1071d others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(57): Show |
3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0179 |
3 | HG01099.hp1 HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.104-1134_104-1071d others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(137): Show |
1 | a0001c0001t0001g0253 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.104-1214_104-1071d others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(184): Show |
1 | a0001c0001t0001g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(193): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(953): Show |
1 | a0001c0001t0001g0085 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(962): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(497): Show |
1 | a0001c0001t0001g0195 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.104-1100_104-1099i others(506): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(73): Show |
1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(81): Show |
1 | a0001c0001t0006g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(90): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(89): Show |
1 | a0001c0001t0004g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(105): Show |
1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(121): Show |
1 | a0001c0001t0004g0223 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(130): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(137): Show |
1 | a0001c0001t0002g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(85): Show |
1 | a0001c0002t0007g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(94): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAA others(293): Show |
1 | a0001c0001t0005g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.104-1220_104-1219i others(302): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | G | GGAAGGAG others(105): Show |
1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-1224_104-1223i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | GGAAGGAA others(9): Show |
G | 2 | a0001c0001t0001g0245 a0001c0001t0039g0034 |
2 | HG00733.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.104-1086_104-1071d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | GGAAGGAA others(121): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0273 |
3 | HG01069.hp2 HG01071.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.104-1198_104-1071d others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | GGAAGGAA others(153): Show |
G | 1 | a0001c0001t0004g0318 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.104-1118_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773486 | GGAAGGAA others(185): Show |
G | 1 | a0003c0004t0002g0210 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.104-1150_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773486 | ||||||
chrX:2773489 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0004g0183 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(361): Show |
1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(370): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(41): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0225 a0001c0001t0001g0262 others(2): Show |
5 | HG00423.hp1 NA18968.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0003g0172 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104-1212_104-1211i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(21): Show |
1 | a0001c0001t0003g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(30): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | AGGAAGGA others(309): Show |
1 | a0001c0001t0001g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.104-1220_104-1219i others(318): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773489 | ||||||
chrX:2773489 | A | G | 1 | a0002c0003t0008g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.104-1227A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773489 | |||||||
chrX:2773502 | A | AGAAGGAA others(313): Show |
1 | a0001c0001t0002g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(322): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773502 | A | AGAAGGAA others(297): Show |
1 | a0001c0001t0016g0293 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773502 | A | AGAAGGAA others(281): Show |
1 | a0001c0001t0006g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(290): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773502 | A | AGAAGGAA others(297): Show |
1 | a0001c0001t0001g0280 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773502 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0005g0288 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.104-1214A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773502 | |||||||
chrX:2773502 | AGAAGGAA others(137): Show |
A | 1 | a0001c0001t0030g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.104-1102_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773502 | AGAAGGAA others(265): Show |
A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.104-1135_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773502 | ||||||
chrX:2773505 | A | AGGAAGGA others(73): Show |
2 | a0001c0001t0001g0171 a0001c0001t0002g0170 |
2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(9): Show |
9 | a0001c0001t0001g0119 a0001c0001t0001g0208 a0001c0001t0002g0141 others(6): Show |
9 | HG00597.hp2 HG00673.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(89): Show |
1 | a0001c0001t0001g0158 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(25): Show |
19 | a0001c0001t0001g0041 a0001c0001t0001g0111 a0001c0001t0001g0130 others(16): Show |
19 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(57): Show |
14 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0155 others(11): Show |
14 | HG00558.hp2 HG00597.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-1196_104-1195i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(89): Show |
1 | a0001c0001t0002g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(185): Show |
1 | a0001c0001t0006g0161 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(194): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(265): Show |
2 | a0001c0001t0004g0191 a0001c0001t0006g0162 |
2 | HG02155.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(233): Show |
1 | a0001c0001t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(57): Show |
2 | a0001c0001t0001g0159 a0001c0001t0027g0167 |
2 | NA18950.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(89): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | NA18944.hp2 NA18968.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.104-1196_104-1195i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | AGGAAGGA others(233): Show |
1 | a0001c0001t0020g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.104-1196_104-1195i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773505 | ||||||
chrX:2773505 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG01981.hp2 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1211A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773505 | |||||||
chrX:2773508 | A | AAGGAAGG others(152): Show |
1 | a0001c0001t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(161): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773508 | ||||||
chrX:2773518 | A | AGAAGGAA others(409): Show |
1 | a0001c0001t0002g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(418): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | AGAAGGAA others(297): Show |
1 | a0001c0001t0002g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(306): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | AGAAGGAA others(633): Show |
1 | a0001c0001t0003g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.104-1119_104-1118i others(642): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | AGAAGGAA others(633): Show |
1 | a0001c0001t0003g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.104-1119_104-1118i others(642): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | AGAAGGAA others(73): Show |
1 | a0001c0001t0020g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104-1135_104-1134i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | AGAGGGAA others(17): Show |
1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104-1196_104-1195i others(26): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | A | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.104-1198A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773518 | |||||||
chrX:2773518 | AGAAGGAA others(121): Show |
A | 4 | a0001c0001t0002g0038 a0001c0001t0006g0175 a0001c0001t0010g0174 others(1): Show |
4 | HG00733.hp2 HG02257.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1086_104-959de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773518 | AGAAGGAA others(249): Show |
A | 4 | a0001c0001t0001g0092 a0001c0001t0017g0270 a0001c0001t0025g0317 others(1): Show |
4 | HG03516.hp1 NA19085.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-1119_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773518 | ||||||
chrX:2773521 | A | AGGAAGGA others(57): Show |
1 | a0001c0001t0003g0251 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104-1148_104-1147i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | AGGAAGGA others(521): Show |
1 | a0001c0001t0003g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.104-1180_104-1179i others(530): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.104-1180_104-1179i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | AGGAAGGA others(73): Show |
2 | a0001c0001t0003g0023 a0001c0001t0003g0024 |
2 | NA18971.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | AGGAAGGA others(25): Show |
2 | a0001c0001t0004g0216 a0001c0001t0004g0220 |
2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | AGGAAGGA others(89): Show |
1 | a0002c0003t0001g0040 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.104-1180_104-1179i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773521 | ||||||
chrX:2773521 | A | G | 63 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.104-1195A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773521 | |||||||
chrX:2773534 | A | AGAAGGAA others(233): Show |
1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.104-1087_104-1086i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | ||||||
chrX:2773534 | A | AGAAGGAA others(409): Show |
1 | a0001c0001t0002g0066 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.104-1164_104-1163i others(418): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | ||||||
chrX:2773534 | A | AGAGGGAA others(1): Show |
3 | a0001c0001t0005g0120 a0001c0002t0005g0126 a0001c0005t0015g0043 |
3 | HG02109.hp1 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.104-1180_104-1179i others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | ||||||
chrX:2773534 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.104-1182A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773534 | |||||||
chrX:2773534 | AGAAGGAA others(105): Show |
A | 11 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0211 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-1054_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773534 | ||||||
chrX:2773537 | A | AGGAAGGA others(361): Show |
1 | a0001c0002t0005g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.104-1164_104-1163i others(370): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773537 | ||||||
chrX:2773537 | A | G | 65 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0067 others(62): Show |
65 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.104-1179A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773537 | |||||||
chrX:2773547 | G | GAGAGAAG others(1193): Show |
1 | a0001c0001t0001g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.104-1116_104-1115i others(1202): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773547 | ||||||
chrX:2773550 | A | AGAAGGAA others(265): Show |
1 | a0001c0001t0006g0073 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | ||||||
chrX:2773550 | A | AGAAGGAA others(233): Show |
1 | a0001c0001t0003g0254 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | ||||||
chrX:2773550 | A | AGAAGGAA others(265): Show |
1 | a0001c0001t0006g0025 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(274): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | ||||||
chrX:2773550 | AGAAGGAA others(89): Show |
A | 9 | a0001c0001t0001g0116 a0001c0001t0001g0234 a0001c0001t0001g0235 others(6): Show |
9 | HG00140.hp1 HG01496.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-1070_104-975de others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | ||||||
chrX:2773550 | AGAAGGAA others(217): Show |
A | 1 | a0001c0001t0024g0087 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.104-1087_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773550 | ||||||
chrX:2773553 | A | AGGAAGGA others(197): Show |
1 | a0001c0001t0011g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-1148_104-1147i others(206): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773553 | ||||||
chrX:2773553 | A | AGGAAGGA others(41): Show |
1 | a0001c0001t0003g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.104-1148_104-1147i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773553 | ||||||
chrX:2773553 | A | G | 40 | a0001c0001t0001g0067 a0001c0001t0001g0129 a0001c0001t0001g0130 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.104-1163A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773553 | |||||||
chrX:2773556 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1160A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773556 | |||||||
chrX:2773566 | A | AGAAGGAA others(281): Show |
1 | a0001c0001t0002g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(290): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | ||||||
chrX:2773566 | A | C | 1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-1150A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773566 | |||||||
chrX:2773566 | AGAAGGAA others(73): Show |
A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0115 a0001c0001t0002g0196 others(3): Show |
6 | HG01361.hp2 HG01934.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-1070_104-991de others(81): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | ||||||
chrX:2773566 | AGAAGGAA others(201): Show |
A | 2 | a0001c0001t0010g0192 a0002c0003t0008g0064 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.104-1071_104-864de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773566 | ||||||
chrX:2773567 | G | GAGGGAGA others(233): Show |
1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1148_104-1147i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773567 | ||||||
chrX:2773569 | A | AGGAAGGA others(169): Show |
1 | a0001c0002t0005g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(178): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773569 | ||||||
chrX:2773569 | A | AGGAAGGA others(57): Show |
1 | a0001c0001t0021g0278 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104-1132_104-1131i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773569 | ||||||
chrX:2773569 | A | G | 43 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0088 others(40): Show |
43 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.104-1147A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773569 | |||||||
chrX:2773572 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1144A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773572 | |||||||
chrX:2773573 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1143A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773573 | |||||||
chrX:2773574 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1142G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773574 | |||||||
chrX:2773577 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1139A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773577 | |||||||
chrX:2773581 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1135G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773581 | |||||||
chrX:2773582 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.104-1134A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773582 | |||||||
chrX:2773582 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-1134A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773582 | |||||||
chrX:2773582 | AGAAGGAA others(57): Show |
A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0238 a0001c0001t0013g0303 others(5): Show |
8 | HG01515.hp2 HG01517.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-1070_104-1007d others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | ||||||
chrX:2773582 | AGAAGGAA others(169): Show |
A | 1 | a0001c0001t0011g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.104-1118_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | ||||||
chrX:2773582 | AGAAGGAA others(185): Show |
A | 2 | a0001c0001t0016g0277 a0001c0001t0024g0182 |
2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.104-1070_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773582 | ||||||
chrX:2773585 | A | AGGAAGGA others(169): Show |
1 | a0001c0001t0005g0120 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(178): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | ||||||
chrX:2773585 | A | AGGAAGGA others(105): Show |
1 | a0001c0001t0003g0059 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.104-1116_104-1115i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | ||||||
chrX:2773585 | A | AGGAAGGA others(473): Show |
1 | a0001c0001t0005g0140 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.104-1116_104-1115i others(482): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773585 | ||||||
chrX:2773585 | A | G | 34 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0129 others(31): Show |
34 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.104-1131A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773585 | |||||||
chrX:2773588 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1128A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773588 | |||||||
chrX:2773598 | A | AGAAGGAA others(89): Show |
1 | a0001c0001t0001g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | ||||||
chrX:2773598 | AGAAGGAA others(41): Show |
A | 14 | a0001c0001t0001g0153 a0001c0001t0001g0264 a0001c0001t0001g0290 others(11): Show |
14 | HG00738.hp2 HG01257.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.104-1070_104-1023d others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | ||||||
chrX:2773598 | AGAAGGAA others(153): Show |
A | 2 | a0001c0001t0001g0105 a0001c0001t0002g0127 |
2 | HG00099.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.104-1102_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | ||||||
chrX:2773598 | AGAAGGAA others(169): Show |
A | 3 | a0001c0001t0001g0203 a0001c0001t0007g0063 a0001c0002t0040g0135 |
3 | HG01070.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.104-1070_104-895de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773598 | ||||||
chrX:2773601 | A | AGGAAGGA others(137): Show |
1 | a0001c0005t0015g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(146): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773601 | ||||||
chrX:2773601 | A | AGGAAGGA others(217): Show |
1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.104-1100_104-1099i others(226): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773601 | ||||||
chrX:2773601 | A | G | 30 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0129 others(27): Show |
30 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.104-1115A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773601 | |||||||
chrX:2773604 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1112A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773604 | |||||||
chrX:2773614 | A | AGAAGGAA others(41): Show |
1 | a0001c0001t0003g0214 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.104-1087_104-1086i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | ||||||
chrX:2773614 | A | C | 12 | a0001c0001t0001g0222 a0001c0001t0001g0280 a0001c0001t0003g0045 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-1102A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773614 | |||||||
chrX:2773614 | AGAAGGAA others(25): Show |
A | 8 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0003g0037 others(5): Show |
8 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-1070_104-1039d others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | ||||||
chrX:2773614 | AGAAGGAA others(137): Show |
A | 1 | a0001c0001t0044g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.104-1086_104-943de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | ||||||
chrX:2773614 | AGAAGGAA others(153): Show |
A | 5 | a0001c0001t0002g0071 a0001c0001t0003g0062 a0001c0001t0014g0095 others(2): Show |
5 | HG02451.hp1 HG02698.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-1070_104-911de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773614 | ||||||
chrX:2773617 | A | AGGAAGAA others(197): Show |
1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.104-1094_104-1093i others(206): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | ||||||
chrX:2773617 | A | AGGAAGGA others(89): Show |
1 | a0001c0001t0001g0316 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.104-1084_104-1083i others(98): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | ||||||
chrX:2773617 | A | AGGAAGGA others(185): Show |
1 | a0001c0001t0005g0284 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.104-1084_104-1083i others(194): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773617 | ||||||
chrX:2773617 | A | G | 19 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0129 others(16): Show |
19 | HG00280.hp1 HG00408.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.104-1099A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773617 | |||||||
chrX:2773630 | A | AGAAGGAA others(57): Show |
1 | a0001c0001t0004g0078 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773630 | A | AGAAGGAA others(73): Show |
1 | a0001c0001t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773630 | A | AGAAGGAA others(329): Show |
1 | a0001c0001t0020g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104-959_104-958ins others(336): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773630 | A | C | 9 | a0001c0001t0001g0187 a0001c0001t0001g0240 a0001c0001t0003g0045 others(6): Show |
9 | HG00438.hp1 HG01361.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1086A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773630 | |||||||
chrX:2773630 | AGAAGGAA others(9): Show |
A | 29 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0067 others(26): Show |
29 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.104-1070_104-1055d others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773630 | AGAAGGAA others(121): Show |
A | 8 | a0001c0001t0001g0222 a0001c0001t0002g0291 a0001c0001t0002g0300 others(5): Show |
8 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-991_104-864del | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773630 | AGAAGGAA others(137): Show |
A | 7 | a0001c0001t0001g0055 a0001c0001t0001g0312 a0001c0001t0002g0118 others(4): Show |
7 | HG00280.hp1 HG00544.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-1070_104-927de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773630 | ||||||
chrX:2773633 | A | AGGAAGGA others(233): Show |
1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.104-1071_104-1070i others(242): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | ||||||
chrX:2773633 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0003g0251 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | ||||||
chrX:2773633 | A | AGGAAGGA others(9): Show |
2 | a0001c0001t0004g0223 a0001c0001t0004g0246 |
2 | NA18952.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.104-1071_104-1070i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | ||||||
chrX:2773633 | A | AGGAAGGA others(25): Show |
1 | a0001c0001t0001g0022 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | ||||||
chrX:2773633 | A | AGGAAGGA others(73): Show |
1 | a0001c0001t0019g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.104-1071_104-1070i others(82): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773633 | ||||||
chrX:2773633 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0213 others(11): Show |
14 | HG00642.hp1 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-1083A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773633 | |||||||
chrX:2773636 | A | AAGGAAGG others(24): Show |
1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.104-1072_104-1071i others(33): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773636 | ||||||
chrX:2773644 | AGCGAAGG others(186): Show |
A | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-1071_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773644 | |||||||
chrX:2773646 | C | A | 165 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(162): Show |
165 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.104-1070C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773646 | |||||||
chrX:2773646 | C | CGAAGGAA others(9): Show |
1 | a0001c0001t0011g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-974_104-959dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773646 | C | CGAAGGAA others(89): Show |
1 | a0001c0002t0007g0276 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104-1054_104-959du others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773646 | C | CGAAGGAA others(57): Show |
1 | a0001c0001t0006g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.104-1055_104-1054i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773646 | C | CGAAGGAA others(457): Show |
1 | a0002c0003t0007g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.104-1055_104-1054i others(466): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773646 | CGAAGGAA others(41): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0003g0297 |
2 | HG03239.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.104-1006_104-959de others(49): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773646 | CGAAGGAA others(89): Show |
C | 1 | a0001c0001t0029g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.104-1054_104-959de others(97): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773646 | ||||||
chrX:2773649 | A | AGGAAGGA others(56): Show |
1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-1042_104-1041i others(65): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | AGGAAGGA others(153): Show |
1 | a0001c0001t0036g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.104-1004_104-1003i others(162): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | AGGAAGGA others(25): Show |
1 | a0001c0001t0004g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.104-1036_104-1035i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | AGGAAGGA others(41): Show |
6 | a0001c0001t0001g0111 a0001c0001t0001g0259 a0001c0001t0001g0267 others(3): Show |
6 | NA18747.hp2 NA18947.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-1036_104-1035i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | AGGAAGGA others(25): Show |
1 | a0001c0001t0029g0279 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.104-1052_104-1051i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | AGGAAGGA others(121): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.104-1052_104-1051i others(130): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773649 | ||||||
chrX:2773649 | A | G | 14 | a0001c0001t0001g0129 a0001c0001t0001g0195 a0001c0001t0001g0213 others(11): Show |
14 | HG01168.hp1 HG02109.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-1067A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773649 | |||||||
chrX:2773652 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1064A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773652 | |||||||
chrX:2773662 | A | C | 8 | a0001c0001t0001g0215 a0001c0001t0002g0096 a0001c0001t0004g0318 others(5): Show |
8 | HG00423.hp2 HG01261.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-1054A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773662 | |||||||
chrX:2773662 | AGAAGGAA others(105): Show |
A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0212 others(3): Show |
6 | HG00438.hp1 HG03688.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-975_104-864del | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773662 | ||||||
chrX:2773665 | A | AGGAAGGA others(57): Show |
1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.104-1004_104-1003i others(66): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | ||||||
chrX:2773665 | A | AGGAAGGA others(41): Show |
3 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0004g0220 |
3 | NA18961.hp1 NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.104-1020_104-1019i others(50): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | ||||||
chrX:2773665 | A | AGGAAGGA others(25): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0226 a0001c0001t0001g0265 |
3 | HG00323.hp2 NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.104-1036_104-1035i others(34): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | ||||||
chrX:2773665 | A | AGGAAGGA others(105): Show |
1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.104-1036_104-1035i others(114): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773665 | ||||||
chrX:2773665 | A | G | 15 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0139 others(12): Show |
15 | HG00438.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.104-1051A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773665 | |||||||
chrX:2773668 | A | AAGGAAGG others(8): Show |
1 | a0001c0001t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104-1040_104-1039i others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773668 | ||||||
chrX:2773668 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-1048A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773668 | |||||||
chrX:2773670 | GGAAGGAG others(8): Show |
G | 1 | a0001c0001t0001g0296 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.104-1044_104-1030d others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773670 | ||||||
chrX:2773678 | A | AGAAGGAA others(377): Show |
2 | a0002c0003t0026g0310 a0002c0003t0026g0311 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.104-1007_104-1006i others(386): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773678 | ||||||
chrX:2773678 | A | C | 7 | a0001c0001t0001g0116 a0001c0001t0001g0215 a0001c0001t0001g0245 others(4): Show |
7 | HG00423.hp2 HG00733.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-1038A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773678 | |||||||
chrX:2773678 | AGAAGGAA others(89): Show |
A | 6 | a0001c0001t0001g0213 a0001c0001t0001g0250 a0001c0001t0001g0304 others(3): Show |
6 | HG02258.hp2 HG02683.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.104-959_104-864del others(96): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773678 | ||||||
chrX:2773681 | A | G | 10 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.104-1035A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773681 | |||||||
chrX:2773692 | AGAGAAGG others(138): Show |
A | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.104-1023_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773692 | |||||||
chrX:2773694 | A | AGAAGGAA others(265): Show |
1 | a0002c0003t0008g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.104-975_104-974ins others(272): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | ||||||
chrX:2773694 | A | AGAAGGAA others(277): Show |
1 | a0001c0001t0028g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-1004_104-1003i others(286): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | ||||||
chrX:2773694 | A | AGAAGGAA others(9): Show |
1 | a0001c0001t0002g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.104-1007_104-1006i others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | ||||||
chrX:2773694 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.104-1022A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773694 | |||||||
chrX:2773694 | AGAAGGAA others(73): Show |
A | 1 | a0001c0002t0012g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.104-958_104-879del others(80): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773694 | ||||||
chrX:2773697 | A | AGGAAGGA others(265): Show |
1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104-988_104-987ins others(272): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | ||||||
chrX:2773697 | A | AGGAAGGA others(153): Show |
1 | a0001c0001t0003g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104-991_104-990ins others(160): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | ||||||
chrX:2773697 | A | AGGAAGGA others(249): Show |
1 | a0001c0001t0005g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.104-1004_104-1003i others(258): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773697 | ||||||
chrX:2773697 | A | G | 9 | a0001c0001t0001g0129 a0001c0001t0003g0059 a0001c0001t0003g0283 others(6): Show |
9 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.104-1019A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773697 | |||||||
chrX:2773708 | AGAGAAGG others(122): Show |
A | 1 | a0001c0001t0021g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.104-1007_104-879de others(1): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773708 | |||||||
chrX:2773710 | A | AGAAGGAA others(41): Show |
1 | a0002c0003t0031g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.104-975_104-974ins others(48): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773710 | ||||||
chrX:2773710 | A | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0181 a0001c0001t0001g0204 |
3 | HG00323.hp1 HG02273.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.104-1006A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773710 | |||||||
chrX:2773710 | AGAAGGAA others(57): Show |
A | 6 | a0001c0001t0001g0036 a0001c0001t0009g0103 a0001c0001t0016g0233 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-958_104-895del others(64): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773710 | ||||||
chrX:2773713 | A | AGGAAGGA others(281): Show |
1 | a0001c0001t0005g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.104-988_104-987ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773713 | ||||||
chrX:2773713 | A | AGGAAGGA others(281): Show |
2 | a0001c0001t0023g0004 a0001c0001t0023g0006 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.104-988_104-987ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773713 | ||||||
chrX:2773713 | A | G | 12 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0139 others(9): Show |
12 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.104-1003A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773713 | |||||||
chrX:2773718 | G | GGAAGGAG others(316): Show |
1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-988_104-987ins others(323): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773718 | ||||||
chrX:2773722 | G | GGAGAGAA others(175): Show |
1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-980_104-979ins others(182): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773722 | ||||||
chrX:2773726 | A | AGAAGGAA others(9): Show |
1 | a0001c0001t0012g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.104-975_104-974ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | ||||||
chrX:2773726 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0181 others(1): Show |
4 | HG02273.hp1 HG02630.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-990A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773726 | |||||||
chrX:2773726 | AGAAGGAA others(25): Show |
A | 1 | a0001c0001t0001g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.104-974_104-943del others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | ||||||
chrX:2773726 | AGAAGGAA others(41): Show |
A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0088 a0001c0001t0001g0119 others(5): Show |
8 | HG02071.hp1 HG02165.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-958_104-911del others(48): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773726 | ||||||
chrX:2773729 | A | AGGAAGGA others(281): Show |
1 | a0001c0002t0007g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.104-972_104-971ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773729 | ||||||
chrX:2773729 | A | G | 13 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0139 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.104-987A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773729 | |||||||
chrX:2773742 | A | AGAAGGAA others(245): Show |
1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104-966_104-965ins others(252): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | ||||||
chrX:2773742 | A | AGAAGGAA others(9): Show |
5 | a0001c0001t0001g0054 a0001c0001t0003g0214 a0001c0001t0004g0078 others(2): Show |
5 | HG02074.hp1 HG02129.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-942_104-927dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | ||||||
chrX:2773742 | A | C | 25 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(22): Show |
25 | HG00408.hp2 HG00733.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.104-974A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773742 | |||||||
chrX:2773742 | AGAAGGAA others(9): Show |
A | 1 | a0001c0001t0001g0273 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.104-942_104-927del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | ||||||
chrX:2773742 | AGAAGGAA others(25): Show |
A | 1 | a0001c0001t0003g0143 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.104-958_104-927del others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773742 | ||||||
chrX:2773744 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-972A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773744 | |||||||
chrX:2773745 | A | AGGAAGGA others(361): Show |
1 | a0001c0001t0022g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.104-959_104-958ins others(368): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773745 | ||||||
chrX:2773745 | A | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0001g0138 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.104-971A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773745 | |||||||
chrX:2773758 | C | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0052 others(110): Show |
114 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.104-958C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773758 | |||||||
chrX:2773758 | C | CGAAGGAA others(9): Show |
3 | a0001c0001t0005g0288 a0001c0002t0007g0276 a0004c0008t0035g0282 |
3 | HG01891.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.104-943_104-942ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | ||||||
chrX:2773758 | C | CGAAGGAA others(57): Show |
1 | a0001c0001t0005g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104-943_104-942ins others(64): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | ||||||
chrX:2773758 | C | CGAAGGAA others(441): Show |
1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104-943_104-942ins others(448): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | ||||||
chrX:2773758 | C | CGAAGGAA others(25): Show |
1 | a0001c0001t0002g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.104-942_104-911dup others(32): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773758 | ||||||
chrX:2773758 | C | G | 1 | a0001c0001t0028g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.104-958C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773758 | |||||||
chrX:2773761 | A | G | 9 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0001g0138 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-955A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773761 | |||||||
chrX:2773773 | G | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-943G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773773 | |||||||
chrX:2773774 | C | A | 61 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0067 others(58): Show |
61 | HG00408.hp1 HG00609.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.104-942C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773774 | |||||||
chrX:2773774 | C | CGAAGGAA others(9): Show |
2 | a0001c0001t0001g0018 a0001c0001t0005g0284 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.104-879_104-864dup others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | ||||||
chrX:2773774 | C | CGAAGGAA others(281): Show |
1 | a0001c0001t0001g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.104-927_104-926ins others(288): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | ||||||
chrX:2773774 | CGAAGGAA others(9): Show |
C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0226 a0001c0001t0003g0251 others(1): Show |
4 | HG00323.hp2 HG00423.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.104-879_104-864del others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773774 | ||||||
chrX:2773777 | A | AGGAAGGA others(457): Show |
1 | a0001c0002t0007g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.104-864_104-863ins others(464): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773777 | ||||||
chrX:2773777 | A | AGGAAGGA others(9): Show |
1 | a0001c0001t0003g0012 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.104-924_104-923ins others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773777 | ||||||
chrX:2773777 | A | G | 17 | a0001c0001t0001g0052 a0001c0001t0001g0092 a0001c0001t0001g0129 others(14): Show |
17 | HG02080.hp1 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.104-939A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773777 | |||||||
chrX:2773790 | A | AGAAGGAA others(617): Show |
1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104-864_104-863ins others(624): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773790 | ||||||
chrX:2773790 | A | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0195 a0001c0001t0001g0203 others(9): Show |
12 | HG00673.hp1 HG01070.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.104-926A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773790 | |||||||
chrX:2773793 | A | AGGAAGGA others(105): Show |
1 | a0001c0001t0036g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.104-908_104-907ins others(112): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773793 | ||||||
chrX:2773793 | A | G | 10 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0005g0140 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-923A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773793 | |||||||
chrX:2773809 | A | G | 8 | a0001c0001t0002g0109 a0001c0001t0007g0063 a0001c0001t0010g0192 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.104-907A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773809 | |||||||
chrX:2773823 | G | A | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-893G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773823 | |||||||
chrX:2773824 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-892A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773824 | |||||||
chrX:2773825 | A | G | 1 | a0001c0001t0017g0270 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.104-891A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773825 | |||||||
chrX:2773828 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.104-888A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773828 | |||||||
chrX:2773830 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.104-886G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773830 | |||||||
chrX:2773835 | GAGAGAAG others(10): Show |
G | 1 | a0001c0001t0004g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.104-877_104-861del others(17): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2773835 | ||||||
chrX:2773839 | G | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-877G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773839 | |||||||
chrX:2773841 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-875A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773841 | |||||||
chrX:2773844 | A | G | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.104-872A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773844 | |||||||
chrX:2773844 | A | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-872A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773844 | |||||||
chrX:2773847 | G | A | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-869G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773847 | |||||||
chrX:2773849 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-867A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773849 | |||||||
chrX:2773850 | G | A | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-866G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773850 | |||||||
chrX:2773857 | G | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-859G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773857 | |||||||
chrX:2773865 | A | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-851A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773865 | |||||||
chrX:2773871 | G | A | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-845G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773871 | |||||||
chrX:2773872 | G | T | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-844G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773872 | |||||||
chrX:2773873 | A | G | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-843A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773873 | |||||||
chrX:2773885 | C | A | 1 | a0001c0001t0004g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.104-831C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773885 | |||||||
chrX:2773896 | A | G | 11 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0020g0132 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.104-820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773896 | |||||||
chrX:2773932 | A | T | 1 | a0001c0001t0011g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.104-784A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2773932 | |||||||
chrX:2774018 | A | ACC | 14 | a0001c0001t0001g0055 a0001c0001t0001g0092 a0001c0001t0001g0213 others(11): Show |
14 | HG00280.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.104-696_104-695dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774018 | ||||||
chrX:2774021 | C | CCT | 5 | a0001c0001t0001g0129 a0001c0001t0003g0283 a0001c0001t0020g0132 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-695_104-694ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774021 | |||||||
chrX:2774084 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.104-632C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774084 | |||||||
chrX:2774330 | G | GAAAGAAA others(329): Show |
1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(336): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774330 | G | GAAAGAAA others(326): Show |
1 | a0002c0003t0031g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(333): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774330 | G | GAAAGAAA others(324): Show |
6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0020g0147 others(3): Show |
6 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-372_104-371ins others(331): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774330 | G | GAAAGAAA others(325): Show |
2 | a0001c0002t0034g0010 a0002c0003t0007g0009 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.104-372_104-371ins others(332): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774330 | G | GAAAGAAA others(338): Show |
3 | a0001c0001t0001g0129 a0001c0001t0020g0132 a0001c0002t0005g0032 |
3 | HG02109.hp2 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.104-372_104-371ins others(345): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774330 | G | GAAAGAAA others(341): Show |
1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104-372_104-371ins others(348): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774330 | ||||||
chrX:2774355 | T | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.104-361T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774355 | |||||||
chrX:2774399 | CT | C | 5 | a0001c0001t0003g0062 a0001c0001t0005g0003 a0001c0001t0005g0019 others(2): Show |
5 | HG01261.hp1 HG02630.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.104-316delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774399 | |||||||
chrX:2774416 | G | A | 1 | a0001c0001t0003g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.104-300G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774416 | |||||||
chrX:2774420 | A | G | 116 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.104-296A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774420 | |||||||
chrX:2774422 | C | CCCTGTG | 169 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.104-293_104-288dup others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 2774422 | ||||||
chrX:2774439 | G | A | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.104-277G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774439 | |||||||
chrX:2774556 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(171): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.104-160T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774556 | |||||||
chrX:2774669 | A | G | 93 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.104-47A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774669 | |||||||
chrX:2774703 | T | C | 2 | a0001c0001t0001g0129 a0001c0002t0005g0032 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.104-13T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 2/10 | chrX | 2774703 | |||||||
chrX:2774958 | C | G | 1 | a0001c0001t0043g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+219C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2774958 | |||||||
chrX:2775026 | G | C | 14 | a0001c0001t0001g0287 a0001c0001t0003g0045 a0001c0001t0003g0046 others(11): Show |
14 | HG00099.hp1 HG00140.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.127+287G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775026 | |||||||
chrX:2775070 | T | C | 6 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0025g0317 others(3): Show |
6 | HG00741.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+331T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775070 | |||||||
chrX:2775071 | C | G | 4 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0002t0007g0050 others(1): Show |
4 | HG02257.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+332C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775071 | |||||||
chrX:2775075 | C | A | 6 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0025g0317 others(3): Show |
6 | HG00741.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+336C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775075 | |||||||
chrX:2775120 | C | G | 2 | a0001c0001t0003g0062 a0001c0002t0005g0275 |
2 | HG02698.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.127+381C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775120 | |||||||
chrX:2775124 | G | T | 1 | a0001c0002t0007g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127+385G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775124 | |||||||
chrX:2775134 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(171): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.127+395A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775134 | |||||||
chrX:2775583 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(165): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.127+844G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775583 | |||||||
chrX:2775618 | A | C | 16 | a0001c0001t0001g0092 a0001c0001t0003g0133 a0001c0001t0005g0140 others(13): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.127+879A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775618 | |||||||
chrX:2775664 | G | C | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+925G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775664 | |||||||
chrX:2775783 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.127+1044T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775783 | |||||||
chrX:2775863 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0013g0309 a0001c0001t0025g0317 |
3 | HG01884.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.127+1124A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775863 | |||||||
chrX:2775866 | G | A | 1 | a0001c0001t0013g0309 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127+1127G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775866 | |||||||
chrX:2775966 | AAAAAAAG | A | 11 | a0001c0001t0001g0116 a0001c0001t0001g0153 a0001c0001t0001g0184 others(8): Show |
11 | HG01517.hp1 HG01884.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+1232_127+1238d others(9): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775966 | ||||||
chrX:2775967 | AAAAAAG | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.127+1233_127+1238d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775967 | ||||||
chrX:2775968 | AAAAAG | A | 28 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0002g0257 others(25): Show |
28 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+1249_127+1253d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2775968 | ||||||
chrX:2775972 | AG | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0226 |
3 | HG00323.hp2 NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.127+1234delG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2775972 | |||||||
chrX:2776014 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127+1275G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776014 | |||||||
chrX:2776100 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.127+1361T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776100 | |||||||
chrX:2776137 | G | GCCACA | 168 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(165): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.127+1399_127+1400i others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776137 | ||||||
chrX:2776160 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127+1421T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776160 | |||||||
chrX:2776163 | A | C | 24 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0092 others(21): Show |
24 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.127+1424A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776163 | |||||||
chrX:2776171 | G | C | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.127+1432G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776171 | |||||||
chrX:2776199 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(275): Show |
279 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.127+1460G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776199 | |||||||
chrX:2776208 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.127+1469T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776208 | |||||||
chrX:2776211 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0002g0141 a0001c0001t0005g0305 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+1472T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776211 | |||||||
chrX:2776262 | T | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0261 a0001c0001t0003g0283 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.127+1523T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776262 | |||||||
chrX:2776321 | A | G | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.127+1582A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776321 | |||||||
chrX:2776328 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.127+1589C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776328 | |||||||
chrX:2776357 | G | C | 7 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0020g0147 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+1618G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776357 | |||||||
chrX:2776370 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0028g0026 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.127+1631T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776370 | |||||||
chrX:2776370 | TACAAGGT others(1): Show |
T | 4 | a0001c0001t0002g0127 a0001c0001t0003g0219 a0002c0003t0026g0310 others(1): Show |
4 | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1633_127+1640d others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776370 | ||||||
chrX:2776388 | G | A | 132 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(129): Show |
132 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.127+1649G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776388 | |||||||
chrX:2776446 | A | C | 6 | a0003c0004t0001g0227 a0003c0004t0001g0228 a0003c0004t0002g0056 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+1707A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776446 | |||||||
chrX:2776492 | C | T | 11 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0007g0063 others(8): Show |
11 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.127+1753C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776492 | |||||||
chrX:2776553 | T | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.127+1814T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776553 | |||||||
chrX:2776564 | G | C | 1 | a0001c0006t0032g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127+1825G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776564 | |||||||
chrX:2776608 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.127+1869A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776608 | |||||||
chrX:2776709 | A | G | 8 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0005g0030 others(5): Show |
8 | HG02559.hp1 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+1970A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776709 | |||||||
chrX:2776716 | C | T | 11 | a0001c0001t0001g0315 a0001c0001t0003g0045 a0001c0001t0003g0046 others(8): Show |
11 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.127+1977C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776716 | |||||||
chrX:2776739 | T | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0230 a0001c0001t0003g0099 others(3): Show |
6 | HG00408.hp1 NA18940.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.127+2000T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776739 | |||||||
chrX:2776765 | G | A | 67 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0082 others(64): Show |
67 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.127+2026G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776765 | |||||||
chrX:2776772 | C | T | 48 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0092 others(45): Show |
48 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.127+2033C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776772 | |||||||
chrX:2776780 | G | A | 22 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0003g0133 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(19): Show |
intron_variant | MODIFIER | c.127+2041G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776780 | |||||||
chrX:2776796 | C | A | 16 | a0001c0001t0003g0283 a0001c0001t0005g0029 a0001c0001t0005g0030 others(13): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.127+2057C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776796 | |||||||
chrX:2776845 | TCAA | T | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0092 others(30): Show |
33 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.127+2122_127+2124d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2776845 | ||||||
chrX:2776990 | C | T | 1 | a0001c0001t0028g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127+2251C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2776990 | |||||||
chrX:2777133 | G | A | 1 | a0001c0001t0028g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.127+2394G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777133 | |||||||
chrX:2777150 | C | A | 5 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2411C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777150 | |||||||
chrX:2777174 | A | T | 7 | a0002c0007t0037g0097 a0003c0004t0001g0227 a0003c0004t0001g0228 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+2435A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777174 | |||||||
chrX:2777243 | G | T | 5 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2504G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777243 | |||||||
chrX:2777299 | A | G | 9 | a0001c0001t0001g0315 a0001c0001t0003g0045 a0001c0001t0003g0046 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+2560A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777299 | |||||||
chrX:2777410 | CA | C | 5 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2679delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777410 | ||||||
chrX:2777459 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127+2720G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777459 | |||||||
chrX:2777598 | T | TA | 5 | a0001c0001t0022g0005 a0001c0001t0023g0004 a0001c0001t0023g0006 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.127+2868dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2777598 | ||||||
chrX:2777759 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127+3020G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777759 | |||||||
chrX:2777789 | A | G | 42 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.127+3050A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777789 | |||||||
chrX:2777819 | A | G | 42 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.127+3080A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777819 | |||||||
chrX:2777823 | A | G | 16 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0284 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.127+3084A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777823 | |||||||
chrX:2777857 | G | A | 5 | a0001c0001t0001g0211 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01175.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.127+3118G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777857 | |||||||
chrX:2777990 | G | T | 1 | a0001c0001t0009g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.127+3251G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2777990 | |||||||
chrX:2778304 | A | C | 1 | a0002c0003t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127+3565A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778304 | |||||||
chrX:2778358 | C | T | 4 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0284 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+3619C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778358 | |||||||
chrX:2778389 | A | T | 3 | a0001c0001t0005g0030 a0001c0001t0005g0284 a0001c0002t0005g0285 |
3 | HG02559.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127+3650A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778389 | |||||||
chrX:2778511 | C | T | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128-3555C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778511 | |||||||
chrX:2778519 | G | A | 41 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.128-3547G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778519 | |||||||
chrX:2778625 | G | T | 8 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0022g0005 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-3441G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778625 | |||||||
chrX:2778758 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.128-3308C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778758 | |||||||
chrX:2778775 | C | CT | 6 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0002g0071 others(3): Show |
6 | HG03516.hp1 NA18939.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3275dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778775 | ||||||
chrX:2778775 | C | T | 8 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0022g0005 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.128-3291C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778775 | |||||||
chrX:2778775 | CT | C | 23 | a0001c0001t0001g0107 a0001c0001t0001g0315 a0001c0001t0003g0045 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-3275delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2778775 | ||||||
chrX:2778804 | C | T | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-3262C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778804 | |||||||
chrX:2778805 | G | A | 24 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(21): Show |
24 | HG01074.hp1 HG01109.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.128-3261G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778805 | |||||||
chrX:2778851 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(26): Show |
29 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.128-3215G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778851 | |||||||
chrX:2778852 | C | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0315 a0001c0001t0002g0314 others(26): Show |
29 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.128-3214C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778852 | |||||||
chrX:2778866 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0022g0005 a0001c0001t0023g0004 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3200C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2778866 | |||||||
chrX:2779038 | A | G | 1 | a0001c0001t0003g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.128-3028A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779038 | |||||||
chrX:2779060 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-3006A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779060 | |||||||
chrX:2779113 | A | C | 22 | a0001c0001t0001g0092 a0001c0001t0001g0304 a0001c0001t0002g0314 others(19): Show |
22 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.128-2953A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779113 | |||||||
chrX:2779169 | A | C | 1 | a0001c0001t0002g0274 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.128-2897A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779169 | |||||||
chrX:2779277 | A | G | 26 | a0001c0001t0001g0287 a0001c0001t0001g0315 a0001c0001t0003g0045 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.128-2789A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779277 | |||||||
chrX:2779312 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2754G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779312 | |||||||
chrX:2779330 | TA | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0088 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.128-2718delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | ||||||
chrX:2779330 | TAA | T | 22 | a0001c0001t0001g0092 a0001c0001t0002g0314 a0001c0001t0003g0059 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.128-2719_128-2718d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | ||||||
chrX:2779330 | TAAA | T | 15 | a0001c0001t0001g0315 a0001c0001t0003g0045 a0001c0001t0003g0046 others(12): Show |
15 | HG00741.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-2720_128-2718d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2779330 | ||||||
chrX:2779333 | A | T | 1 | a0001c0001t0006g0016 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.128-2733A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779333 | |||||||
chrX:2779450 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.128-2616G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779450 | |||||||
chrX:2779550 | G | A | 1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-2516G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779550 | |||||||
chrX:2779558 | C | A | 1 | a0001c0001t0006g0016 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.128-2508C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779558 | |||||||
chrX:2779650 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.128-2416T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779650 | |||||||
chrX:2779669 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2397C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779669 | |||||||
chrX:2779739 | C | T | 5 | a0001c0001t0001g0211 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG01175.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2327C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779739 | |||||||
chrX:2779796 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.128-2270G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779796 | |||||||
chrX:2779804 | C | T | 25 | a0001c0001t0001g0092 a0001c0001t0001g0287 a0001c0001t0001g0315 others(22): Show |
25 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-2262C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779804 | |||||||
chrX:2779827 | G | A | 23 | a0001c0001t0001g0287 a0001c0001t0001g0315 a0001c0001t0003g0045 others(20): Show |
23 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.128-2239G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779827 | |||||||
chrX:2779835 | C | T | 1 | a0001c0001t0008g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.128-2231C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779835 | |||||||
chrX:2779936 | C | T | 1 | a0001c0002t0042g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-2130C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2779936 | |||||||
chrX:2780064 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0002g0294 |
2 | NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.128-2002T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780064 | |||||||
chrX:2780129 | G | T | 1 | a0001c0001t0012g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.128-1937G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780129 | |||||||
chrX:2780150 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.128-1916A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780150 | |||||||
chrX:2780185 | A | G | 6 | a0001c0001t0001g0287 a0001c0001t0007g0063 a0001c0001t0010g0192 others(3): Show |
6 | HG02717.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-1881A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780185 | |||||||
chrX:2780288 | AAAG | A | 7 | a0002c0007t0037g0097 a0003c0004t0001g0227 a0003c0004t0001g0228 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1773_128-1771d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780288 | ||||||
chrX:2780409 | C | CT | 17 | a0001c0001t0001g0092 a0001c0001t0001g0261 a0001c0001t0004g0112 others(14): Show |
17 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.128-1643dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780409 | ||||||
chrX:2780409 | CT | C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0088 others(16): Show |
19 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-1643delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780409 | ||||||
chrX:2780423 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0004g0068 |
2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.128-1643T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780423 | |||||||
chrX:2780424 | C | T | 7 | a0001c0001t0001g0187 a0001c0001t0004g0068 a0001c0001t0007g0063 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1642C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780424 | |||||||
chrX:2780425 | T | A | 2 | a0001c0001t0001g0187 a0001c0001t0004g0068 |
2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.128-1641T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780425 | |||||||
chrX:2780425 | T | C | 5 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0022g0189 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1641T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780425 | |||||||
chrX:2780425 | T | TA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.128-1627dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780425 | ||||||
chrX:2780425 | T | TAA | 8 | a0001c0001t0001g0245 a0001c0001t0002g0148 a0001c0001t0004g0117 others(5): Show |
8 | HG00733.hp1 HG00741.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-1628_128-1627d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780425 | ||||||
chrX:2780426 | A | T | 5 | a0001c0001t0007g0063 a0001c0001t0010g0192 a0001c0001t0022g0189 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-1640A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780426 | |||||||
chrX:2780717 | C | A | 1 | a0001c0001t0003g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128-1349C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780717 | |||||||
chrX:2780725 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0168 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.128-1341A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780725 | |||||||
chrX:2780728 | AAG | A | 19 | a0001c0001t0006g0016 a0001c0001t0019g0186 a0001c0001t0022g0005 others(16): Show |
19 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.128-1336_128-1335d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2780728 | ||||||
chrX:2780882 | G | A | 14 | a0001c0001t0001g0092 a0001c0001t0005g0288 a0001c0001t0019g0186 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.128-1184G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780882 | |||||||
chrX:2780913 | G | A | 30 | a0001c0001t0001g0092 a0001c0001t0001g0287 a0001c0001t0005g0030 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-1153G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2780913 | |||||||
chrX:2781146 | T | C | 138 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
138 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.128-920T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781146 | |||||||
chrX:2781147 | G | C | 136 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.128-919G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781147 | |||||||
chrX:2781148 | T | C | 136 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.128-918T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781148 | |||||||
chrX:2781153 | C | CAAAGGCT others(3): Show |
1 | a0001c0001t0003g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.128-911_128-902dup others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781153 | ||||||
chrX:2781205 | C | A | 82 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.128-861C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781205 | |||||||
chrX:2781234 | T | G | 162 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0039 others(159): Show |
162 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.128-832T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781234 | |||||||
chrX:2781309 | A | T | 119 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(116): Show |
119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.128-757A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781309 | |||||||
chrX:2781319 | T | C | 111 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(108): Show |
111 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.128-747T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781319 | |||||||
chrX:2781409 | A | C | 103 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(100): Show |
103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.128-657A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781409 | |||||||
chrX:2781514 | C | A | 173 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(170): Show |
173 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.128-552C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781514 | |||||||
chrX:2781584 | A | G | 15 | a0001c0001t0001g0315 a0001c0001t0003g0045 a0001c0001t0003g0046 others(12): Show |
15 | HG00741.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.128-482A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781584 | |||||||
chrX:2781604 | G | T | 6 | a0003c0004t0001g0227 a0003c0004t0001g0228 a0003c0004t0002g0056 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-462G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781604 | |||||||
chrX:2781635 | G | A | 104 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(101): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.128-431G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781635 | |||||||
chrX:2781642 | G | A | 1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.128-424G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781642 | |||||||
chrX:2781857 | C | CT | 102 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.128-200dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 2781857 | ||||||
chrX:2781865 | T | G | 9 | a0001c0001t0001g0315 a0001c0001t0003g0045 a0001c0001t0003g0046 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-201T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781865 | |||||||
chrX:2781927 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0035 others(153): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.128-139A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781927 | |||||||
chrX:2781986 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0035 others(141): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-80T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 3/10 | chrX | 2781986 | |||||||
chrX:2782148 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.190+20A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782148 | |||||||
chrX:2782153 | C | G | 1 | a0001c0001t0014g0206 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.190+25C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782153 | |||||||
chrX:2782161 | A | G | 121 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.190+33A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782161 | |||||||
chrX:2782261 | T | A | 119 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(116): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.190+133T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782261 | |||||||
chrX:2782386 | C | G | 1 | a0001c0002t0007g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.190+258C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782386 | |||||||
chrX:2782567 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0035 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.190+439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782567 | |||||||
chrX:2782572 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0035 others(132): Show |
136 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.190+444A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782572 | |||||||
chrX:2782592 | G | T | 1 | a0001c0001t0024g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.190+464G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782592 | |||||||
chrX:2782597 | T | G | 3 | a0001c0001t0028g0026 a0002c0007t0037g0097 a0004c0008t0035g0282 |
3 | HG02922.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.190+469T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782597 | |||||||
chrX:2782735 | T | C | 2 | a0001c0001t0004g0051 a0001c0001t0004g0150 |
2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.190+607T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782735 | |||||||
chrX:2782880 | G | C | 1 | a0001c0001t0021g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+752G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782880 | |||||||
chrX:2782931 | C | T | 3 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.190+803C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782931 | |||||||
chrX:2782963 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0129 others(21): Show |
24 | HG00741.hp1 HG01109.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.190+835T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2782963 | |||||||
chrX:2783032 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.190+904T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783032 | |||||||
chrX:2783042 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.190+914A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783042 | |||||||
chrX:2783144 | C | T | 267 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(264): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.190+1016C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783144 | |||||||
chrX:2783203 | T | C | 1 | a0001c0001t0004g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.190+1075T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783203 | |||||||
chrX:2783314 | C | CA | 142 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0041 others(139): Show |
142 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.190+1192dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783314 | ||||||
chrX:2783354 | A | AG | 7 | a0001c0001t0001g0085 a0001c0001t0001g0116 a0001c0001t0001g0225 others(4): Show |
7 | HG00438.hp2 HG01978.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+1232dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783354 | ||||||
chrX:2783418 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.190+1290T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783418 | |||||||
chrX:2783442 | A | G | 2 | a0001c0002t0005g0126 a0004c0008t0035g0282 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.190+1314A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783442 | |||||||
chrX:2783591 | G | A | 2 | a0001c0001t0014g0206 a0001c0001t0016g0277 |
2 | HG03239.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.190+1463G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783591 | |||||||
chrX:2783658 | A | C | 2 | a0001c0001t0001g0304 a0001c0002t0008g0321 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.190+1530A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783658 | |||||||
chrX:2783795 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0021g0020 others(2): Show |
5 | HG00741.hp1 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+1667C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783795 | |||||||
chrX:2783804 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0021g0020 others(2): Show |
5 | HG00741.hp1 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+1676G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783804 | |||||||
chrX:2783897 | T | C | 2 | a0001c0001t0001g0304 a0001c0005t0015g0049 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.190+1769T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783897 | |||||||
chrX:2783931 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.190+1803T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2783931 | |||||||
chrX:2783976 | AAAACC | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0001t0001g0304 others(2): Show |
5 | HG02129.hp2 HG03453.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+1873_190+1877d others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2783976 | ||||||
chrX:2784001 | C | A | 4 | a0001c0001t0001g0304 a0001c0001t0008g0302 a0001c0001t0025g0317 others(1): Show |
4 | HG01884.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+1873C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784001 | |||||||
chrX:2784006 | A | C | 126 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(123): Show |
126 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.190+1878A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784006 | |||||||
chrX:2784007 | A | C | 1 | a0001c0001t0003g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.190+1879A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784007 | |||||||
chrX:2784034 | C | A | 1 | a0001c0002t0012g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.190+1906C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784034 | |||||||
chrX:2784102 | T | C | 111 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(108): Show |
111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.190+1974T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784102 | |||||||
chrX:2784298 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.190+2170T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784298 | |||||||
chrX:2784429 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.190+2301A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784429 | |||||||
chrX:2784439 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+2311C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784439 | |||||||
chrX:2784527 | G | A | 64 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(61): Show |
64 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.190+2399G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784527 | |||||||
chrX:2784564 | C | T | 8 | a0001c0001t0005g0003 a0001c0001t0005g0029 a0001c0001t0005g0120 others(5): Show |
8 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+2436C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784564 | |||||||
chrX:2784569 | CAAA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(96): Show |
100 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.190+2456_190+2458d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2784569 | ||||||
chrX:2784657 | C | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0129 others(22): Show |
26 | HG00642.hp1 HG00741.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.190+2529C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784657 | |||||||
chrX:2784738 | C | T | 1 | a0001c0001t0006g0025 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190+2610C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784738 | |||||||
chrX:2784758 | C | G | 78 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(75): Show |
78 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.190+2630C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784758 | |||||||
chrX:2784905 | G | T | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(74): Show |
77 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.190+2777G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2784905 | |||||||
chrX:2785130 | G | C | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.190+3002G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785130 | |||||||
chrX:2785164 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.190+3036C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785164 | |||||||
chrX:2785313 | G | C | 64 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0082 others(61): Show |
64 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.190+3185G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785313 | |||||||
chrX:2785332 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+3204C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785332 | |||||||
chrX:2785350 | T | C | 173 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0054 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.190+3222T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785350 | |||||||
chrX:2785459 | A | AT | 104 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0060 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.190+3331_190+3332i others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785459 | |||||||
chrX:2785460 | A | AT | 65 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0082 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.190+3339dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2785460 | ||||||
chrX:2785460 | A | T | 104 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0060 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.190+3332A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785460 | |||||||
chrX:2785503 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.190+3375A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785503 | |||||||
chrX:2785592 | A | G | 169 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0054 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.190+3464A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785592 | |||||||
chrX:2785856 | T | G | 1 | a0001c0001t0004g0068 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.190+3728T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2785856 | |||||||
chrX:2786016 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0287 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.191-3628G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786016 | |||||||
chrX:2786260 | C | CT | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0213 others(14): Show |
17 | HG00741.hp1 HG01243.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.191-3367dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0104 a0001c0001t0001g0252 a0001c0001t0004g0173 others(5): Show |
8 | HG01168.hp1 HG01517.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.191-3375_191-3367d others(11): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(3): Show |
65 | a0001c0001t0001g0014 a0001c0001t0001g0052 a0001c0001t0001g0054 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.191-3376_191-3367d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(4): Show |
29 | a0001c0001t0001g0221 a0001c0001t0001g0234 a0001c0001t0001g0235 others(26): Show |
29 | HG00738.hp2 HG01099.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.191-3377_191-3367d others(13): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0005g0140 a0001c0002t0034g0010 a0001c0002t0040g0135 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-3383_191-3367d others(19): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(11): Show |
29 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0098 others(26): Show |
29 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(20): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(12): Show |
15 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0134 others(12): Show |
15 | HG00323.hp2 HG02486.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(21): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(13): Show |
10 | a0001c0001t0001g0102 a0001c0001t0001g0137 a0001c0001t0003g0062 others(7): Show |
10 | HG01975.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.191-3367_191-3366i others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0003g0200 a0001c0002t0005g0032 |
2 | HG02970.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.191-3367_191-3366i others(24): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786260 | CT | C | 12 | a0001c0001t0001g0035 a0001c0001t0002g0071 a0001c0001t0002g0294 others(9): Show |
12 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.191-3367delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2786260 | ||||||
chrX:2786294 | G | C | 166 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0052 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.191-3350G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786294 | |||||||
chrX:2786428 | T | C | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.191-3216T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786428 | |||||||
chrX:2786483 | G | A | 15 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0005g0019 others(12): Show |
15 | HG00741.hp1 HG01243.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.191-3161G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786483 | |||||||
chrX:2786498 | C | T | 1 | a0001c0002t0007g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.191-3146C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786498 | |||||||
chrX:2786515 | A | G | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.191-3129A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786515 | |||||||
chrX:2786568 | T | C | 188 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.191-3076T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786568 | |||||||
chrX:2786759 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.191-2885G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786759 | |||||||
chrX:2786767 | T | C | 189 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.191-2877T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786767 | |||||||
chrX:2786827 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.191-2817A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786827 | |||||||
chrX:2786948 | T | C | 178 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.191-2696T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786948 | |||||||
chrX:2786970 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(10): Show |
14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-2674C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2786970 | |||||||
chrX:2787109 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0036g0002 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.191-2535C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787109 | |||||||
chrX:2787163 | A | G | 7 | a0001c0001t0005g0003 a0001c0001t0005g0029 a0001c0001t0005g0120 others(4): Show |
7 | HG01074.hp1 HG01261.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-2481A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787163 | |||||||
chrX:2787224 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(10): Show |
14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-2420C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787224 | |||||||
chrX:2787247 | C | G | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2397C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787247 | |||||||
chrX:2787367 | A | G | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2277A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787367 | |||||||
chrX:2787413 | A | G | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2231A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787413 | |||||||
chrX:2787421 | G | A | 60 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0082 others(57): Show |
60 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.191-2223G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787421 | |||||||
chrX:2787423 | T | A | 126 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0022 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.191-2221T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787423 | |||||||
chrX:2787439 | C | T | 2 | a0001c0001t0010g0192 a0001c0001t0020g0147 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.191-2205C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787439 | |||||||
chrX:2787582 | C | T | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-2062C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787582 | |||||||
chrX:2787732 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.191-1912C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787732 | |||||||
chrX:2787809 | G | A | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1835G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787809 | |||||||
chrX:2787822 | G | A | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1822G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787822 | |||||||
chrX:2787838 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.191-1806C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2787838 | |||||||
chrX:2787864 | GCCACTGC others(170): Show |
G | 2 | a0001c0001t0021g0020 a0002c0003t0031g0110 |
2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.191-1754_191-1578d others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787864 | ||||||
chrX:2787907 | CA | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(152): Show |
156 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.191-1718delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | ||||||
chrX:2787907 | CAA | C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0304 a0001c0001t0002g0272 others(4): Show |
7 | HG01070.hp2 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.191-1719_191-1718d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2787907 | ||||||
chrX:2788102 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.191-1542A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788102 | |||||||
chrX:2788102 | AAG | A | 72 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(69): Show |
72 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.191-1532_191-1531d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2788102 | ||||||
chrX:2788172 | G | A | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1472G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788172 | |||||||
chrX:2788275 | G | T | 1 | a0001c0002t0034g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.191-1369G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788275 | |||||||
chrX:2788299 | G | A | 74 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.191-1345G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788299 | |||||||
chrX:2788332 | C | T | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-1312C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788332 | |||||||
chrX:2788446 | G | T | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.191-1198G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788446 | |||||||
chrX:2788745 | C | G | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-899C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788745 | |||||||
chrX:2788798 | T | C | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.191-846T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788798 | |||||||
chrX:2788800 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.191-844A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788800 | |||||||
chrX:2788855 | T | TA | 183 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.191-779dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2788855 | ||||||
chrX:2788903 | A | G | 28 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0134 others(25): Show |
28 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.191-741A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2788903 | |||||||
chrX:2789019 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.191-625A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789019 | |||||||
chrX:2789101 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.191-543T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789101 | |||||||
chrX:2789294 | A | G | 2 | a0001c0001t0001g0137 a0004c0008t0035g0282 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.191-350A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789294 | |||||||
chrX:2789330 | T | C | 2 | a0001c0001t0021g0020 a0002c0003t0031g0110 |
2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.191-314T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789330 | |||||||
chrX:2789459 | T | TAAGTTTA others(14): Show |
62 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0069 others(59): Show |
62 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.191-179_191-178ins others(21): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 2789459 | ||||||
chrX:2789570 | A | T | 2 | a0001c0001t0013g0303 a0001c0001t0013g0307 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.191-74A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 4/10 | chrX | 2789570 | |||||||
chrX:2789729 | T | TTTTTA | 3 | a0001c0001t0001g0296 a0001c0001t0004g0183 a0002c0003t0001g0040 |
3 | HG00408.hp2 NA19054.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.253+49_253+53dupTT others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | ||||||
chrX:2789729 | T | TTTTTATT others(13): Show |
1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+34_253+53dupTT others(18): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | ||||||
chrX:2789729 | TTTTTATT others(3): Show |
T | 12 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.253+44_253+53delTT others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789729 | ||||||
chrX:2789777 | A | C | 2 | a0001c0001t0021g0020 a0002c0003t0031g0110 |
2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.253+71A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789777 | |||||||
chrX:2789783 | TTTTAC | T | 61 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0069 others(58): Show |
61 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.253+82_253+86delCT others(3): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2789783 | ||||||
chrX:2789796 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0046g0122 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.253+90T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789796 | |||||||
chrX:2789930 | G | T | 3 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.253+224G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789930 | |||||||
chrX:2789937 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.253+231T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2789937 | |||||||
chrX:2790001 | T | C | 14 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.253+295T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790001 | |||||||
chrX:2790062 | G | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0005g0019 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+356G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790062 | |||||||
chrX:2790078 | G | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(10): Show |
13 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+372G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790078 | |||||||
chrX:2790093 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253+387C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790093 | |||||||
chrX:2790108 | C | T | 2 | a0001c0001t0021g0020 a0002c0003t0031g0110 |
2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.253+402C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790108 | |||||||
chrX:2790270 | G | A | 1 | a0001c0001t0009g0103 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.253+564G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790270 | |||||||
chrX:2790424 | C | T | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+718C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790424 | |||||||
chrX:2790490 | C | A | 17 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(14): Show |
17 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.253+784C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790490 | |||||||
chrX:2790505 | G | GA | 234 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.253+816dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790505 | ||||||
chrX:2790610 | G | A | 39 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(36): Show |
39 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.253+904G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790610 | |||||||
chrX:2790674 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.253+968C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790674 | |||||||
chrX:2790706 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0004g0068 |
2 | HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.253+1000A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790706 | |||||||
chrX:2790712 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.253+1006A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790712 | |||||||
chrX:2790864 | A | G | 3 | a0001c0001t0020g0132 a0001c0001t0021g0278 a0001c0005t0015g0043 |
3 | HG02109.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.253+1158A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2790864 | |||||||
chrX:2790967 | ATAAATT | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.253+1267_253+1272d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2790967 | ||||||
chrX:2791052 | TTTC | T | 30 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(27): Show |
30 | HG00438.hp1 HG00558.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.253+1349_253+1351d others(5): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791052 | ||||||
chrX:2791183 | C | T | 15 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(12): Show |
15 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.253+1477C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791183 | |||||||
chrX:2791290 | T | A | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253+1584T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791290 | |||||||
chrX:2791524 | CTCCAAAA others(13): Show |
C | 7 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0250 others(4): Show |
7 | HG01123.hp2 HG01433.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+1822_253+1841d others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2791524 | ||||||
chrX:2791559 | C | T | 1 | a0001c0001t0002g0314 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.253+1853C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2791559 | |||||||
chrX:2792059 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.253+2353G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792059 | |||||||
chrX:2792165 | A | G | 2 | a0001c0001t0005g0140 a0001c0005t0015g0049 |
2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.254-2370A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792165 | |||||||
chrX:2792222 | G | C | 1 | a0001c0006t0032g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.254-2313G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792222 | |||||||
chrX:2792270 | T | C | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-2265T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792270 | |||||||
chrX:2792297 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.254-2238C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792297 | |||||||
chrX:2792331 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254-2204C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792331 | |||||||
chrX:2792356 | T | A | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-2179T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792356 | |||||||
chrX:2792380 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254-2155G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792380 | |||||||
chrX:2792446 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.254-2089G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792446 | |||||||
chrX:2792463 | T | G | 6 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0250 others(3): Show |
6 | HG01433.hp2 HG02004.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-2072T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792463 | |||||||
chrX:2792465 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.254-2070G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792465 | |||||||
chrX:2792517 | TTTTCTTT others(3): Show |
T | 1 | a0002c0003t0001g0028 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254-2004_254-1995d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792517 | ||||||
chrX:2792545 | T | TTGTG | 151 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0022 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.254-1968_254-1965d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | ||||||
chrX:2792545 | T | TTGTGTG | 3 | a0001c0001t0001g0015 a0001c0001t0001g0265 a0001c0001t0006g0175 |
3 | NA18950.hp2 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.254-1970_254-1965d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | ||||||
chrX:2792545 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.254-1974_254-1965d others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | ||||||
chrX:2792545 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.254-1978_254-1965d others(16): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | ||||||
chrX:2792545 | TTG | T | 3 | a0001c0001t0001g0267 a0001c0001t0002g0170 a0001c0001t0029g0128 |
3 | HG00621.hp1 NA19084.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.254-1966_254-1965d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 2792545 | ||||||
chrX:2792799 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.254-1736C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792799 | |||||||
chrX:2792846 | G | C | 4 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 others(1): Show |
4 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-1689G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792846 | |||||||
chrX:2792954 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.254-1581C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2792954 | |||||||
chrX:2793146 | C | T | 14 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(11): Show |
14 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.254-1389C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793146 | |||||||
chrX:2793198 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0021g0020 a0002c0003t0031g0110 |
3 | HG00741.hp1 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.254-1337C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793198 | |||||||
chrX:2793388 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.254-1147G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793388 | |||||||
chrX:2793425 | A | G | 3 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.254-1110A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793425 | |||||||
chrX:2793681 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.254-854C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793681 | |||||||
chrX:2793682 | G | A | 6 | a0001c0001t0003g0283 a0001c0001t0007g0063 a0001c0001t0012g0289 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-853G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793682 | |||||||
chrX:2793738 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.254-797G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793738 | |||||||
chrX:2793770 | A | G | 1 | a0001c0001t0009g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.254-765A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793770 | |||||||
chrX:2793920 | G | C | 39 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(36): Show |
39 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.254-615G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2793920 | |||||||
chrX:2794242 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.254-293C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2794242 | |||||||
chrX:2794344 | G | A | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.254-191G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 5/10 | chrX | 2794344 | |||||||
chrX:2794620 | C | T | 36 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(33): Show |
36 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.322+17C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794620 | |||||||
chrX:2794679 | G | T | 1 | a0001c0001t0002g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.322+76G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794679 | |||||||
chrX:2794869 | C | T | 1 | a0002c0003t0031g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.322+266C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794869 | |||||||
chrX:2794971 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+368T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2794971 | |||||||
chrX:2795028 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+425G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795028 | |||||||
chrX:2795032 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.322+429C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795032 | |||||||
chrX:2795048 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.322+445A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795048 | |||||||
chrX:2795098 | T | C | 34 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(31): Show |
34 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.322+495T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795098 | |||||||
chrX:2795147 | T | A | 1 | a0001c0005t0015g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322+544T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795147 | |||||||
chrX:2795170 | G | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.322+567G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795170 | |||||||
chrX:2795240 | G | GTATT | 180 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.322+640_322+641ins others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795240 | ||||||
chrX:2795253 | G | A | 1 | a0001c0002t0008g0321 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.322+650G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795253 | |||||||
chrX:2795482 | CAT | C | 22 | a0001c0001t0001g0134 a0001c0001t0003g0283 a0001c0001t0007g0063 others(19): Show |
22 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.322+882_322+883del others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795482 | ||||||
chrX:2795491 | ATATCTT | A | 33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.322+892_322+897del others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2795491 | ||||||
chrX:2795526 | C | T | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+923C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795526 | |||||||
chrX:2795547 | G | C | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322+944G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795547 | |||||||
chrX:2795561 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.322+958A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795561 | |||||||
chrX:2795657 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.322+1054G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795657 | |||||||
chrX:2795667 | A | T | 1 | a0001c0001t0027g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.322+1064A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795667 | |||||||
chrX:2795671 | T | A | 3 | a0001c0001t0007g0063 a0001c0001t0012g0289 a0001c0001t0045g0121 |
3 | HG01891.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.322+1068T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795671 | |||||||
chrX:2795681 | C | T | 1 | a0001c0001t0003g0241 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.322+1078C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795681 | |||||||
chrX:2795722 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.322+1119A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795722 | |||||||
chrX:2795753 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.322+1150G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795753 | |||||||
chrX:2795766 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(176): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.322+1163T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795766 | |||||||
chrX:2795769 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.322+1166T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795769 | |||||||
chrX:2795935 | C | T | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+1332C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795935 | |||||||
chrX:2795995 | A | C | 2 | a0001c0001t0003g0201 a0001c0001t0003g0214 |
2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.323-1315A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2795995 | |||||||
chrX:2796044 | G | GTA | 34 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(31): Show |
34 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.323-1264_323-1263d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796044 | ||||||
chrX:2796070 | T | C | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.323-1240T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796070 | |||||||
chrX:2796121 | A | G | 33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-1189A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796121 | |||||||
chrX:2796212 | CATAA | C | 33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-1094_323-1091d others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796212 | ||||||
chrX:2796236 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.323-1074C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796236 | |||||||
chrX:2796303 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.323-1007G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796303 | |||||||
chrX:2796468 | A | ATG | 3 | a0001c0001t0001g0304 a0001c0002t0042g0033 a0002c0007t0037g0097 |
3 | HG03453.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.323-822_323-821dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | ||||||
chrX:2796468 | A | ATGTGTG | 120 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0022 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.323-826_323-821dup others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | ||||||
chrX:2796468 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0074 a0001c0001t0001g0315 a0001c0001t0002g0145 others(4): Show |
7 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-828_323-821dup others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | ||||||
chrX:2796468 | A | ATGTGTGT others(3): Show |
15 | a0001c0001t0005g0019 a0001c0001t0005g0044 a0001c0001t0013g0303 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.323-830_323-821dup others(10): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796468 | ||||||
chrX:2796490 | A | ATGTGTGT others(1): Show |
33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-819_323-818ins others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 2796490 | ||||||
chrX:2796490 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.323-820A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796490 | |||||||
chrX:2796492 | A | G | 42 | a0001c0001t0001g0074 a0001c0001t0001g0092 a0001c0001t0001g0107 others(39): Show |
42 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.323-818A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796492 | |||||||
chrX:2796494 | A | G | 36 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(33): Show |
36 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.323-816A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796494 | |||||||
chrX:2796543 | T | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0203 a0001c0001t0002g0127 others(2): Show |
5 | HG00099.hp2 HG01070.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-767T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796543 | |||||||
chrX:2796696 | A | G | 1 | a0002c0003t0031g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.323-614A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796696 | |||||||
chrX:2796715 | T | C | 33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-595T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796715 | |||||||
chrX:2796863 | G | A | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.323-447G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796863 | |||||||
chrX:2796884 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.323-426G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796884 | |||||||
chrX:2796924 | G | A | 35 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(32): Show |
35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.323-386G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2796924 | |||||||
chrX:2797145 | C | A | 5 | a0001c0001t0019g0186 a0001c0001t0021g0020 a0001c0001t0043g0123 others(2): Show |
5 | HG00741.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-165C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2797145 | |||||||
chrX:2797283 | C | T | 33 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.323-27C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 6/10 | chrX | 2797283 | |||||||
chrX:2797379 | A | C | 1 | a0001c0001t0019g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.373+19A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797379 | |||||||
chrX:2797384 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.373+24A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797384 | |||||||
chrX:2797422 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.373+62C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797422 | |||||||
chrX:2797514 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.373+154G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797514 | |||||||
chrX:2797586 | G | GCA | 38 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(35): Show |
38 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.373+248_373+249dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2797586 | ||||||
chrX:2797759 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.373+399C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797759 | |||||||
chrX:2797789 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0304 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.373+429T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797789 | |||||||
chrX:2797829 | T | G | 35 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(32): Show |
35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+469T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797829 | |||||||
chrX:2797936 | A | T | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+576A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797936 | |||||||
chrX:2797958 | T | G | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+598T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2797958 | |||||||
chrX:2798159 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0046g0122 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.373+799T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798159 | |||||||
chrX:2798305 | G | A | 35 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(32): Show |
35 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+945G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798305 | |||||||
chrX:2798369 | C | CT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0113 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.373+1029dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | ||||||
chrX:2798369 | CT | C | 16 | a0001c0001t0001g0092 a0001c0001t0001g0137 a0001c0001t0003g0084 others(13): Show |
16 | HG01070.hp2 HG01074.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.373+1029delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | ||||||
chrX:2798369 | CTT | C | 31 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0134 others(28): Show |
31 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.373+1028_373+1029d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798369 | ||||||
chrX:2798373 | T | C | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0003g0237 others(2): Show |
5 | HG01175.hp1 HG01361.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+1013T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798373 | |||||||
chrX:2798374 | T | C | 1 | a0001c0001t0024g0087 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.373+1014T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798374 | |||||||
chrX:2798570 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.373+1210C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798570 | |||||||
chrX:2798872 | T | TTTTTTC | 6 | a0001c0001t0005g0140 a0001c0001t0007g0063 a0001c0001t0021g0020 others(3): Show |
6 | HG00741.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+1522_373+1527d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798872 | ||||||
chrX:2798885 | T | TTTTTC | 29 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0134 others(26): Show |
29 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.373+1527_373+1528i others(7): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798885 | ||||||
chrX:2798886 | T | TTTTC | 3 | a0001c0001t0001g0108 a0001c0002t0005g0275 a0001c0002t0007g0308 |
3 | HG01168.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.373+1527_373+1528i others(6): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2798886 | ||||||
chrX:2798888 | C | T | 38 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0108 others(35): Show |
38 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.373+1528C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798888 | |||||||
chrX:2798925 | G | A | 1 | a0001c0001t0009g0131 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.373+1565G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798925 | |||||||
chrX:2798992 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+1632A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2798992 | |||||||
chrX:2799026 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.373+1666T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799026 | |||||||
chrX:2799116 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.373+1756G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799116 | |||||||
chrX:2799193 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+1833C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799193 | |||||||
chrX:2799354 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373+1994G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799354 | |||||||
chrX:2799497 | A | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.373+2137A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799497 | |||||||
chrX:2799579 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.373+2219G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799579 | |||||||
chrX:2799617 | G | A | 3 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.373+2257G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799617 | |||||||
chrX:2799635 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0019g0186 a0001c0001t0043g0123 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.373+2275G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2799635 | |||||||
chrX:2800025 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2665T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800025 | |||||||
chrX:2800028 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2668C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800028 | |||||||
chrX:2800030 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2670T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800030 | |||||||
chrX:2800094 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.373+2734T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800094 | |||||||
chrX:2800114 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.373+2754A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800114 | |||||||
chrX:2800139 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.373+2779A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800139 | |||||||
chrX:2800357 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+2997G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800357 | |||||||
chrX:2800558 | T | C | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.373+3198T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800558 | |||||||
chrX:2800652 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3292G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800652 | |||||||
chrX:2800653 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3293A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2800653 | |||||||
chrX:2800975 | C | CA | 82 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0067 others(79): Show |
82 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.373+3638dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | ||||||
chrX:2800975 | C | CAA | 6 | a0001c0001t0003g0185 a0001c0001t0003g0200 a0001c0001t0019g0186 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+3637_373+3638d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | ||||||
chrX:2800975 | CA | C | 25 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0229 others(22): Show |
25 | HG00733.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.373+3638delA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2800975 | ||||||
chrX:2801070 | G | T | 107 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0067 others(104): Show |
107 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.373+3710G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801070 | |||||||
chrX:2801109 | G | A | 1 | a0001c0001t0004g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3749G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801109 | |||||||
chrX:2801111 | C | T | 1 | a0001c0001t0004g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3751C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801111 | |||||||
chrX:2801113 | T | G | 1 | a0001c0001t0004g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3753T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801113 | |||||||
chrX:2801114 | G | C | 1 | a0001c0001t0004g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3754G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801114 | |||||||
chrX:2801116 | T | A | 1 | a0001c0001t0004g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.373+3756T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801116 | |||||||
chrX:2801150 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.373+3790T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801150 | |||||||
chrX:2801201 | CTG | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.373+3842_373+3843d others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801201 | |||||||
chrX:2801257 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.373+3897A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801257 | |||||||
chrX:2801334 | A | AG | 8 | a0001c0001t0003g0283 a0001c0001t0007g0063 a0001c0001t0008g0302 others(5): Show |
8 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.373+3977dupG | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801334 | ||||||
chrX:2801341 | GAGAGAA | G | 3 | a0001c0001t0025g0317 a0001c0001t0028g0026 a0001c0001t0041g0190 |
3 | HG02280.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.373+3987_373+3992d others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801341 | ||||||
chrX:2801447 | G | A | 1 | a0001c0006t0032g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.373+4087G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801447 | |||||||
chrX:2801625 | G | A | 32 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(29): Show |
32 | HG00621.hp1 HG01175.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.373+4265G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801625 | |||||||
chrX:2801717 | A | AT | 20 | a0001c0001t0001g0137 a0001c0001t0003g0185 a0001c0001t0005g0019 others(17): Show |
20 | HG01070.hp2 HG01071.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.373+4366dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2801717 | ||||||
chrX:2801731 | C | T | 19 | a0001c0001t0001g0137 a0001c0001t0005g0019 a0001c0001t0005g0044 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.373+4371C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801731 | |||||||
chrX:2801739 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.373+4379C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801739 | |||||||
chrX:2801747 | C | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0138 others(7): Show |
11 | HG01069.hp2 HG01071.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.373+4387C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801747 | |||||||
chrX:2801747 | C | T | 5 | a0001c0001t0005g0019 a0001c0001t0005g0044 a0001c0002t0005g0032 others(2): Show |
5 | HG02109.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+4387C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801747 | |||||||
chrX:2801762 | G | A | 9 | a0001c0001t0005g0019 a0001c0001t0005g0044 a0001c0001t0023g0004 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.373+4402G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801762 | |||||||
chrX:2801763 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.373+4403C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801763 | |||||||
chrX:2801769 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0226 |
2 | HG00323.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.373+4409C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801769 | |||||||
chrX:2801771 | T | C | 20 | a0001c0001t0001g0137 a0001c0001t0005g0019 a0001c0001t0005g0044 others(17): Show |
20 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.373+4411T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801771 | |||||||
chrX:2801772 | C | G | 21 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0005g0019 others(18): Show |
21 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.373+4412C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801772 | |||||||
chrX:2801799 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.373+4439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801799 | |||||||
chrX:2801810 | G | A | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.373+4450G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801810 | |||||||
chrX:2801814 | T | C | 1 | a0001c0001t0014g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.373+4454T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801814 | |||||||
chrX:2801854 | G | A | 9 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0085 others(6): Show |
9 | HG00438.hp1 HG00738.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.373+4494G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801854 | |||||||
chrX:2801856 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0036g0002 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.373+4496C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801856 | |||||||
chrX:2801898 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.373+4538G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801898 | |||||||
chrX:2801918 | A | G | 79 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0067 others(76): Show |
79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.373+4558A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801918 | |||||||
chrX:2801924 | A | G | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.373+4564A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801924 | |||||||
chrX:2801929 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.373+4569G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801929 | |||||||
chrX:2801950 | G | A | 6 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+4590G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801950 | |||||||
chrX:2801955 | C | T | 6 | a0001c0001t0013g0303 a0001c0001t0013g0307 a0001c0001t0013g0309 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+4595C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801955 | |||||||
chrX:2801977 | G | A | 2 | a0002c0003t0026g0310 a0002c0003t0026g0311 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.373+4617G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801977 | |||||||
chrX:2801986 | C | G | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(32): Show |
35 | HG00621.hp1 HG01175.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.373+4626C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801986 | |||||||
chrX:2801998 | C | T | 1 | a0001c0001t0027g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.373+4638C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2801998 | |||||||
chrX:2802173 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.374-4528T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802173 | |||||||
chrX:2802543 | C | T | 4 | a0001c0001t0003g0283 a0002c0003t0026g0310 a0002c0003t0026g0311 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.374-4158C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802543 | |||||||
chrX:2802661 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.374-4040A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802661 | |||||||
chrX:2802845 | A | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0315 |
2 | HG00733.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.374-3856A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2802845 | |||||||
chrX:2803216 | A | G | 22 | a0001c0001t0001g0304 a0001c0001t0005g0019 a0001c0001t0005g0044 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.374-3485A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803216 | |||||||
chrX:2803276 | C | T | 2 | a0001c0001t0019g0186 a0001c0001t0043g0123 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.374-3425C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803276 | |||||||
chrX:2803302 | C | G | 7 | a0001c0001t0001g0304 a0001c0001t0013g0303 a0001c0001t0013g0307 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-3399C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803302 | |||||||
chrX:2803372 | G | A | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.374-3329G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803372 | |||||||
chrX:2803543 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.374-3158G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803543 | |||||||
chrX:2803601 | G | A | 20 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0005g0019 others(17): Show |
20 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-3100G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803601 | |||||||
chrX:2803605 | G | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.374-3096G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803605 | |||||||
chrX:2803747 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.374-2954A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803747 | |||||||
chrX:2803921 | C | A | 5 | a0001c0001t0010g0192 a0001c0001t0020g0132 a0001c0001t0020g0147 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-2780C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803921 | |||||||
chrX:2803937 | G | C | 79 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0067 others(76): Show |
79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.374-2764G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803937 | |||||||
chrX:2803983 | C | T | 2 | a0001c0001t0013g0303 a0001c0001t0013g0307 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.374-2718C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2803983 | |||||||
chrX:2804015 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(151): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.374-2686A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804015 | |||||||
chrX:2804134 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.374-2567C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804134 | |||||||
chrX:2804173 | T | G | 20 | a0001c0001t0001g0304 a0001c0001t0005g0019 a0001c0001t0005g0044 others(17): Show |
20 | HG01070.hp2 HG01071.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-2528T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804173 | |||||||
chrX:2804195 | A | T | 1 | a0001c0001t0002g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.374-2506A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804195 | |||||||
chrX:2804474 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0006g0080 a0001c0001t0029g0279 |
3 | HG00438.hp2 NA18959.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.374-2227A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804474 | |||||||
chrX:2804548 | C | T | 1 | a0001c0002t0008g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.374-2153C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804548 | |||||||
chrX:2804557 | C | T | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.374-2144C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804557 | |||||||
chrX:2804697 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0036g0002 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.374-2004G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804697 | |||||||
chrX:2804813 | G | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0253 a0001c0001t0004g0068 |
3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1888G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804813 | |||||||
chrX:2804842 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0253 a0001c0001t0004g0068 |
3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1859A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804842 | |||||||
chrX:2804846 | A | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0253 a0001c0001t0004g0068 |
3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1855A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804846 | |||||||
chrX:2804854 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0253 a0001c0001t0004g0068 |
3 | HG01123.hp2 HG02273.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.374-1847G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804854 | |||||||
chrX:2804965 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.374-1736C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2804965 | |||||||
chrX:2805203 | G | A | 2 | a0001c0001t0021g0020 a0001c0001t0021g0278 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.374-1498G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805203 | |||||||
chrX:2805259 | C | T | 1 | a0001c0001t0011g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.374-1442C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805259 | |||||||
chrX:2805262 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.374-1439C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805262 | |||||||
chrX:2805509 | C | T | 20 | a0001c0001t0001g0304 a0001c0001t0003g0045 a0001c0001t0003g0046 others(17): Show |
20 | HG00408.hp2 HG00741.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.374-1192C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805509 | |||||||
chrX:2805610 | C | T | 6 | a0001c0001t0001g0208 a0001c0001t0001g0250 a0001c0001t0001g0264 others(3): Show |
6 | HG01433.hp2 HG02004.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-1091C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805610 | |||||||
chrX:2805625 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.374-1076C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805625 | |||||||
chrX:2805634 | A | G | 9 | a0001c0001t0012g0289 a0002c0003t0001g0028 a0002c0003t0001g0136 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.374-1067A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805634 | |||||||
chrX:2805674 | T | G | 64 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(61): Show |
64 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.374-1027T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805674 | |||||||
chrX:2805835 | A | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0089 a0001c0001t0001g0296 others(3): Show |
6 | HG02074.hp1 HG02129.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.374-866A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2805835 | |||||||
chrX:2806120 | T | C | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.374-581T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806120 | |||||||
chrX:2806126 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.374-575C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806126 | |||||||
chrX:2806130 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.374-571C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806130 | |||||||
chrX:2806220 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.374-481C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806220 | |||||||
chrX:2806348 | T | A | 64 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(61): Show |
64 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.374-353T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806348 | |||||||
chrX:2806349 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.374-352A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806349 | |||||||
chrX:2806388 | A | C | 61 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(58): Show |
61 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.374-313A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806388 | |||||||
chrX:2806398 | CT | C | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0059 others(3): Show |
6 | HG02055.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.374-294delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 2806398 | ||||||
chrX:2806407 | T | A | 61 | a0001c0001t0001g0069 a0001c0001t0001g0113 a0001c0001t0001g0115 others(58): Show |
61 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.374-294T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806407 | |||||||
chrX:2806505 | C | A | 1 | a0002c0003t0008g0064 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.374-196C>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 7/10 | chrX | 2806505 | |||||||
chrX:2806995 | C | CAT | 164 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0069 others(161): Show |
164 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.418+250_418+251ins others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2806995 | |||||||
chrX:2806996 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+251G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2806996 | |||||||
chrX:2807006 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+261A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807006 | |||||||
chrX:2807009 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+264C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807009 | |||||||
chrX:2807011 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418+266T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807011 | |||||||
chrX:2807051 | G | A | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0059 others(3): Show |
6 | HG02055.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+306G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807051 | |||||||
chrX:2807133 | C | CTG | 301 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.418+391_418+392dup others(2): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2807133 | ||||||
chrX:2807258 | A | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.418+513A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807258 | |||||||
chrX:2807477 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.419-708T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807477 | |||||||
chrX:2807502 | A | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(281): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.419-683A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807502 | |||||||
chrX:2807504 | ACATGTGC others(15): Show |
A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(280): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.419-667_419-646del others(22): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 2807504 | ||||||
chrX:2807619 | T | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(207): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.419-566T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807619 | |||||||
chrX:2807743 | G | A | 1 | a0001c0002t0012g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.419-442G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807743 | |||||||
chrX:2807750 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(279): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.419-435T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807750 | |||||||
chrX:2807842 | T | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.419-343T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807842 | |||||||
chrX:2807906 | T | C | 5 | a0001c0001t0005g0003 a0001c0001t0005g0029 a0001c0001t0005g0030 others(2): Show |
5 | HG01261.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-279T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2807906 | |||||||
chrX:2808104 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.419-81C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 8/10 | chrX | 2808104 | |||||||
chrX:2808329 | G | A | 9 | a0001c0001t0001g0195 a0001c0001t0004g0112 a0001c0001t0004g0194 others(6): Show |
9 | NA18948.hp1 NA18952.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.454+109G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808329 | |||||||
chrX:2808355 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.454+135A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808355 | |||||||
chrX:2808606 | T | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.454+386T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808606 | |||||||
chrX:2808745 | C | T | 1 | a0001c0001t0003g0251 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.454+525C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808745 | |||||||
chrX:2808772 | C | T | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.454+552C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2808772 | |||||||
chrX:2809210 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.454+990G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809210 | |||||||
chrX:2809457 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454+1237C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809457 | |||||||
chrX:2809632 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0003g0062 |
2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.454+1412C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809632 | |||||||
chrX:2809757 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.454+1537G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809757 | |||||||
chrX:2809794 | C | T | 1 | a0001c0001t0009g0103 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.455-1542C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809794 | |||||||
chrX:2809893 | T | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.455-1443T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2809893 | |||||||
chrX:2810023 | C | T | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.455-1313C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810023 | |||||||
chrX:2810180 | A | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(286): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.455-1156A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810180 | |||||||
chrX:2810218 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.455-1118C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810218 | |||||||
chrX:2810475 | T | C | 91 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0082 others(88): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.455-861T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810475 | |||||||
chrX:2810520 | T | C | 12 | a0001c0001t0002g0170 a0001c0001t0006g0025 a0001c0001t0006g0058 others(9): Show |
12 | HG00438.hp2 HG02080.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.455-816T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810520 | |||||||
chrX:2810777 | A | G | 3 | a0001c0001t0001g0134 a0001c0005t0015g0043 a0001c0005t0015g0049 |
3 | HG02809.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.455-559A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810777 | |||||||
chrX:2810831 | G | A | 94 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0082 others(91): Show |
94 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-505G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810831 | |||||||
chrX:2810855 | G | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-481G>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810855 | |||||||
chrX:2810859 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-477T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810859 | |||||||
chrX:2810862 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-474A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810862 | |||||||
chrX:2810865 | G | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-471G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810865 | |||||||
chrX:2810868 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-468A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810868 | |||||||
chrX:2810871 | A | C | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-465A>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810871 | |||||||
chrX:2810872 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.455-464C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810872 | |||||||
chrX:2810882 | T | A | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-454T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810882 | |||||||
chrX:2810911 | G | A | 2 | a0001c0005t0015g0043 a0001c0005t0015g0049 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.455-425G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810911 | |||||||
chrX:2810912 | T | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-424T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810912 | |||||||
chrX:2810925 | TAAGA | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0005t0015g0043 others(1): Show |
4 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-408_455-405del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810925 | ||||||
chrX:2810926 | A | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-410A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810926 | |||||||
chrX:2810928 | GAAAT | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.455-384_455-381del others(4): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810928 | ||||||
chrX:2810928 | GAAATAAA others(1): Show |
G | 94 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0082 others(91): Show |
94 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-388_455-381del others(8): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2810928 | ||||||
chrX:2810930 | A | T | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-406A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810930 | |||||||
chrX:2810940 | T | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-396T>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810940 | |||||||
chrX:2810965 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.455-371A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810965 | |||||||
chrX:2810970 | A | T | 96 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0082 others(93): Show |
96 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.455-366A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2810970 | |||||||
chrX:2811115 | CT | C | 171 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0069 others(168): Show |
171 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.455-212delT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 2811115 | ||||||
chrX:2811172 | C | G | 2 | a0001c0001t0004g0216 a0001c0001t0004g0220 |
2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.455-164C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811172 | |||||||
chrX:2811240 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.455-96A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811240 | |||||||
chrX:2811243 | C | T | 2 | a0001c0005t0015g0043 a0001c0005t0015g0049 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.455-93C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811243 | |||||||
chrX:2811305 | G | A | 102 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0082 others(99): Show |
102 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.455-31G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 9/10 | chrX | 2811305 | |||||||
chrX:2811495 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571+43G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811495 | |||||||
chrX:2811499 | T | A | 1 | a0001c0002t0005g0285 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.571+47T>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811499 | |||||||
chrX:2811499 | T | TA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.571+58dupA | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2811499 | ||||||
chrX:2811706 | T | C | 2 | a0001c0001t0021g0020 a0001c0001t0021g0278 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.571+254T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811706 | |||||||
chrX:2811721 | G | A | 1 | a0001c0001t0004g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.571+269G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811721 | |||||||
chrX:2811820 | T | C | 1 | a0001c0001t0025g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.571+368T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811820 | |||||||
chrX:2811880 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571+428G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2811880 | |||||||
chrX:2812017 | C | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0090 |
2 | NA18980.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.571+565C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812017 | |||||||
chrX:2812078 | A | AGCCAAAT others(5): Show |
137 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.571+626_571+627ins others(12): Show |
XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812078 | |||||||
chrX:2812079 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.571+627C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812079 | |||||||
chrX:2812232 | C | T | 1 | a0001c0001t0010g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571+780C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812232 | |||||||
chrX:2812248 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.571+796G>A | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812248 | |||||||
chrX:2812675 | C | G | 2 | a0001c0001t0001g0105 a0001c0001t0039g0034 |
2 | NA18946.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.571+1223C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812675 | |||||||
chrX:2812790 | C | T | 1 | a0004c0008t0035g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.571+1338C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2812790 | |||||||
chrX:2813498 | G | C | 1 | a0001c0001t0004g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.572-866G>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813498 | |||||||
chrX:2813519 | C | G | 1 | a0002c0007t0037g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.572-845C>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813519 | |||||||
chrX:2813720 | T | C | 62 | a0001c0001t0001g0129 a0001c0001t0001g0171 a0001c0001t0002g0066 others(59): Show |
62 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.572-644T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813720 | |||||||
chrX:2813764 | T | C | 1 | a0002c0003t0007g0009 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572-600T>C | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813764 | |||||||
chrX:2813788 | A | G | 2 | a0001c0001t0025g0027 a0001c0001t0025g0317 |
2 | HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.572-576A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2813788 | |||||||
chrX:2814055 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.572-309C>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814055 | |||||||
chrX:2814125 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.572-239A>T | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814125 | |||||||
chrX:2814166 | A | G | 27 | a0001c0001t0001g0287 a0001c0001t0001g0312 a0001c0001t0003g0045 others(24): Show |
27 | HG00408.hp2 HG00544.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.572-198A>G | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | chrX | 2814166 | |||||||
chrX:2814315 | C | CT | 233 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
234 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.572-39dupT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814315 | ||||||
chrX:2814315 | C | CTT | 70 | a0001c0001t0001g0129 a0001c0001t0001g0171 a0001c0001t0002g0066 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.572-40_572-39dupTT | XG | ENSG00000124343.14 | transcript | ENST00000644266.2 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 2814315 |