Item | Value |
---|---|
geneid | 57596 |
ensemblid | ENSG00000183092.18 |
hgncid | 24163 |
symbol | BEGAIN |
name | brain enriched guanylate kinase associated |
refseq_nuc | NM_001385089.1 |
refseq_prot | NP_001372018.1 |
ensembl_nuc | ENST00000554140.3 |
ensembl_prot | ENSP00000451125.2 |
mane_status | MANE Select |
chr | chr14 |
start | 100537147 |
end | 100587417 |
strand | - |
ver | v1.2 |
region | chr14:100537147-100587417 |
region5000 | chr14:100532147-100592417 |
regionname0 | BEGAIN_chr14_100537147_100587417 |
regionname5000 | BEGAIN_chr14_100532147_100592417 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 612 | 320 | 96 | 57 | 128 | 9 | 28 | 85 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(607): Show |
chr14 | 100532147 | 100592417 |
a0002 | 0/0 | 612 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(607): Show |
chr14 | 100532147 | 100592417 |
a0003 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(607): Show |
chr14 | 100532147 | 100592417 |
a0004 | 0/0 | 612 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(607): Show |
chr14 | 100532147 | 100592417 |
a0005 | 0/0 | 616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(611): Show |
chr14 | 100532147 | 100592417 |
a0006 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | MWTGG others(607): Show |
chr14 | 100532147 | 100592417 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1836 | 157 | 39 | 36 | 72 | 2 | 8 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0002 | 1/1 | 1836 | 93 | 4 | 20 | 41 | 6 | 20 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0003 | 0/0 | 1836 | 31 | 29 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0004 | 0/0 | 1836 | 18 | 6 | 0 | 12 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0005 | 0/0 | 1836 | 13 | 13 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0006 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0008 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0009 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0012 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0013 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0001c0016 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0002c0007 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0003c0015 | 0/0 | 1836 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0004c0011 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 | ||
a0005c0014 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1843): Show |
chr14 | 100532147 | 100592417 | ||
a0006c0010 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | ATGTG others(1831): Show |
chr14 | 100532147 | 100592417 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2788 | 148 | 39 | 36 | 65 | 2 | 6 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0005 | 0/0 | 2789 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2784): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0007 | 0/0 | 2788 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0008 | 0/0 | 2788 | 2 | 0 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0011 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0013 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0001t0014 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0001 | 0/1 | 2788 | 82 | 4 | 19 | 37 | 6 | 15 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0004 | 1/0 | 2788 | 5 | 0 | 0 | 2 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0005 | 0/0 | 2789 | 2 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2784): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0006 | 0/0 | 2788 | 2 | 0 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0012 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0002t0015 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2784): Show |
chr14 | 100532147 | 100592417 |
a0001c0003t0001 | 0/0 | 2788 | 27 | 25 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0003t0005 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2784): Show |
chr14 | 100532147 | 100592417 |
a0001c0003t0006 | 0/0 | 2788 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0004t0001 | 0/0 | 2788 | 4 | 1 | 0 | 3 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0004t0002 | 0/0 | 2788 | 4 | 4 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0004t0003 | 0/0 | 2788 | 9 | 0 | 0 | 9 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0004t0017 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0005t0001 | 0/0 | 2788 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0005t0002 | 0/0 | 2788 | 8 | 8 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0005t0010 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0005t0016 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0006t0001 | 0/0 | 2788 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0008t0001 | 0/0 | 2788 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0009t0001 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0012t0001 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0013t0001 | 0/0 | 2788 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0001c0016t0001 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0002c0007t0001 | 0/0 | 2788 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0003c0015t0001 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0004c0011t0009 | 0/0 | 2788 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
a0005c0014t0001 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2795): Show |
chr14 | 100532147 | 100592417 |
a0006c0010t0001 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | GCTCC others(2783): Show |
chr14 | 100532147 | 100592417 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0002 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0006g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0012g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0015g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0017g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0016g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0008t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0008t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0009t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0012t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0013t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0016t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0002c0007t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0002c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0003c0015t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0004c0011t0009g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0005c0014t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0006c0010t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0013 | t0001 | g0234 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0094 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00423 | hp1 | a0002 | c0007 | t0001 | g0262 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00544 | hp1 | a0001 | c0016 | t0001 | g0182 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0183 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01081 | hp2 | a0001 | c0012 | t0001 | g0130 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0284 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01261 | hp2 | a0003 | c0015 | t0001 | g0132 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01517 | hp1 | a0004 | c0011 | t0009 | g0023 | EUR | IBS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0224 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01891 | hp2 | a0001 | c0005 | t0002 | g0218 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02055 | hp1 | a0001 | c0008 | t0001 | g0200 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02055 | hp2 | a0001 | c0005 | t0002 | g0109 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02056 | hp2 | a0001 | c0004 | t0003 | g0275 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02129 | hp1 | a0001 | c0001 | t0011 | g0060 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CDX | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | CDX | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02258 | hp1 | a0001 | c0005 | t0010 | g0107 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02280 | hp1 | a0001 | c0005 | t0002 | g0022 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0276 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0221 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02615 | hp1 | a0001 | c0003 | t0005 | g0282 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0240 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02622 | hp2 | a0001 | c0005 | t0001 | g0106 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0242 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02647 | hp2 | a0001 | c0005 | t0001 | g0233 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0291 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02723 | hp2 | a0001 | c0005 | t0002 | g0252 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0286 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0279 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02809 | hp2 | a0001 | c0004 | t0002 | g0006 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0243 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0272 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0215 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0203 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03130 | hp1 | a0001 | c0005 | t0002 | g0253 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0198 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03195 | hp1 | a0001 | c0009 | t0001 | g0102 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03209 | hp1 | a0001 | c0003 | t0006 | g0288 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0110 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0241 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0022 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03579 | hp2 | a0001 | c0004 | t0002 | g0006 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0189 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0159 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03942 | hp1 | a0001 | c0002 | t0006 | g0287 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0188 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0134 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0222 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0098 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18522 | hp1 | a0001 | c0005 | t0016 | g0285 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18747 | hp1 | a0001 | c0002 | t0004 | g0091 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18906 | hp1 | a0001 | c0005 | t0002 | g0219 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18906 | hp2 | a0001 | c0003 | t0006 | g0289 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18940 | hp2 | a0001 | c0002 | t0012 | g0141 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18942 | hp2 | a0005 | c0014 | t0001 | g0037 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18948 | hp1 | a0001 | c0002 | t0015 | g0280 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18959 | hp2 | a0006 | c0010 | t0001 | g0184 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18964 | hp2 | a0001 | c0004 | t0003 | g0191 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18973 | hp1 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18979 | hp2 | a0001 | c0004 | t0003 | g0266 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18984 | hp2 | a0001 | c0004 | t0003 | g0270 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18985 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18995 | hp2 | a0001 | c0004 | t0003 | g0264 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19003 | hp1 | a0002 | c0007 | t0001 | g0034 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19003 | hp2 | a0001 | c0004 | t0003 | g0129 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19030 | hp1 | a0001 | c0005 | t0002 | g0254 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19060 | hp1 | a0001 | c0004 | t0003 | g0267 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19060 | hp2 | a0001 | c0001 | t0013 | g0086 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19068 | hp2 | a0001 | c0004 | t0003 | g0100 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19084 | hp2 | a0001 | c0004 | t0003 | g0265 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19085 | hp1 | a0001 | c0001 | t0014 | g0248 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19088 | hp2 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19240 | hp1 | a0001 | c0008 | t0001 | g0209 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0166 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0162 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0185 | SAS | GIH | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0006 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03471 | hp1 | a0001 | c0004 | t0017 | g0290 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0273 | REF | REF | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0092 | REF | REF | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100538045 | G | A | 1 | a0002 | 2 | HG00423.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.1763C>T | p.Pro588Leu | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1890/2788 | 1763/1839 | 588/612 | chr14 | 100538045 | |||
chr14:100538903 | T | TGGAAGCC others(5): Show |
1 | a0005 | 1 | NA18942.hp2 | conservative_inframe_insertion | MODERATE | c.893_904dupCGGCGGGC others(4): Show |
p.Pro298_Phe301dup | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1031/2788 | 904/1839 | 302/612 | chr14 | 100538903 | |||
chr14:100539098 | G | T | 1 | a0004 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.710C>A | p.Pro237Gln | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 837/2788 | 710/1839 | 237/612 | chr14 | 100539098 | |||
chr14:100539168 | G | C | 1 | a0003 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.640C>G | p.Leu214Val | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 767/2788 | 640/1839 | 214/612 | chr14 | 100539168 | |||
chr14:100539219 | C | T | 1 | a0006 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.589G>A | p.Val197Ile | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 716/2788 | 589/1839 | 197/612 | chr14 | 100539219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100538095 | G | A | 2 | a0001c0004 a0001c0005 |
31 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
synonymous_variant | LOW | c.1713C>T | p.Ala571Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1840/2788 | 1713/1839 | 571/612 | chr14 | 100538095 | |||
chr14:100538218 | G | A | 1 | a0001c0008 | 2 | HG02055.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1717/2788 | 1590/1839 | 530/612 | chr14 | 100538218 | |||
chr14:100538344 | G | A | 1 | a0001c0012 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.1464C>T | p.Ala488Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1591/2788 | 1464/1839 | 488/612 | chr14 | 100538344 | |||
chr14:100538878 | T | C | 10 | a0001c0001 a0001c0003 a0001c0004 others(7): Show |
227 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(224): Show |
synonymous_variant | LOW | c.930A>G | p.Ala310Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1057/2788 | 930/1839 | 310/612 | chr14 | 100538878 | |||
chr14:100538899 | A | G | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
synonymous_variant | LOW | c.909T>C | p.His303His | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1036/2788 | 909/1839 | 303/612 | chr14 | 100538899 | |||
chr14:100538902 | C | T | 1 | a0001c0016 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.906G>A | p.Gln302Gln | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1033/2788 | 906/1839 | 302/612 | chr14 | 100538902 | |||
chr14:100539094 | C | T | 1 | a0001c0006 | 2 | HG02886.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.714G>A | p.Arg238Arg | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 841/2788 | 714/1839 | 238/612 | chr14 | 100539094 | |||
chr14:100543867 | T | C | 4 | a0001c0003 a0001c0004 a0001c0008 others(1): Show |
52 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(49): Show |
synonymous_variant | LOW | c.399A>G | p.Ser133Ser | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/7 | 526/2788 | 399/1839 | 133/612 | chr14 | 100543867 | |||
chr14:100543918 | A | C | 1 | a0001c0009 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.348T>G | p.Val116Val | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/7 | 475/2788 | 348/1839 | 116/612 | chr14 | 100543918 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100537308 | G | A | 1 | a0001c0001t0011 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 661 | chr14 | 100537308 | ||||||
chr14:100537341 | C | A | 1 | a0001c0001t0008 | 2 | HG02602.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 628 | chr14 | 100537341 | ||||||
chr14:100537557 | C | T | 1 | a0001c0005t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 412 | chr14 | 100537557 | ||||||
chr14:100537619 | A | G | 1 | a0001c0004t0003 | 9 | HG02056.hp2 NA18964.hp2 NA18979.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*350T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 350 | chr14 | 100537619 | ||||||
chr14:100537664 | C | A | 1 | a0001c0002t0015 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 305 | chr14 | 100537664 | ||||||
chr14:100537667 | T | G | 1 | a0001c0002t0012 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 302 | chr14 | 100537667 | ||||||
chr14:100537765 | C | G | 33 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(30): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 204 | chr14 | 100537765 | ||||||
chr14:100537839 | G | A | 1 | a0001c0001t0013 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 130 | chr14 | 100537839 | ||||||
chr14:100537947 | G | A | 1 | a0001c0001t0014 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 22 | chr14 | 100537947 | ||||||
chr14:100537956 | T | C | 3 | a0001c0004t0002 a0001c0004t0017 a0001c0005t0002 |
13 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*13A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 13 | chr14 | 100537956 | ||||||
chr14:100587336 | G | GC | 4 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0015 others(1): Show |
6 | HG01192.hp1 HG02615.hp1 HG02738.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-47dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 47 | chr14 | 100587336 | ||||||
chr14:100587339 | C | T | 1 | a0001c0001t0007 | 2 | NA18977.hp2 NA19083.hp1 |
5_prime_UTR_variant | MODIFIER | c.-49G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 49 | chr14 | 100587339 | ||||||
chr14:100587348 | C | T | 1 | a0004c0011t0009 | 1 | HG01517.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 58 | chr14 | 100587348 | ||||||
chr14:100587360 | G | C | 1 | a0001c0005t0016 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 70 | chr14 | 100587360 | ||||||
chr14:100587397 | G | A | 3 | a0001c0002t0006 a0001c0003t0006 a0001c0004t0017 |
6 | HG02717.hp2 HG02735.hp1 HG03209.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 107 | chr14 | 100587397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100539329 | G | A | 2 | a0001c0004t0001g0021 a0001c0004t0001g0268 |
3 | NA18973.hp1 NA18985.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.493-14C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539329 | |||||||
chr14:100539554 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.493-239G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539554 | |||||||
chr14:100539558 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.493-243G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539558 | |||||||
chr14:100539612 | G | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493-297C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539612 | |||||||
chr14:100539649 | C | A | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-334G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539649 | |||||||
chr14:100539763 | A | G | 3 | a0001c0003t0001g0007 a0001c0003t0001g0205 a0001c0003t0001g0278 |
5 | HG02451.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-448T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539763 | |||||||
chr14:100539780 | G | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
24 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.493-465C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539780 | |||||||
chr14:100539900 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.493-585G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539900 | |||||||
chr14:100539929 | C | T | 2 | a0001c0006t0001g0198 a0001c0006t0001g0272 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.492+567G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539929 | |||||||
chr14:100539969 | G | A | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.492+527C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539969 | |||||||
chr14:100539985 | G | A | 3 | a0001c0004t0002g0006 a0001c0004t0002g0203 a0001c0004t0017g0290 |
5 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+511C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539985 | |||||||
chr14:100539998 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.492+498C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539998 | |||||||
chr14:100540026 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0036 |
3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.492+470G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540026 | |||||||
chr14:100540166 | C | T | 4 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0004t0001g0241 others(1): Show |
4 | HG00544.hp1 HG03453.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+330G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540166 | |||||||
chr14:100540208 | G | T | 3 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0016t0001g0182 |
3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.492+288C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540208 | |||||||
chr14:100540363 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.492+133C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540363 | |||||||
chr14:100540641 | C | T | 2 | a0001c0002t0001g0035 a0001c0002t0001g0173 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.409-62G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540641 | |||||||
chr14:100540735 | C | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.409-156G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540735 | |||||||
chr14:100540786 | C | T | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-207G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540786 | |||||||
chr14:100540934 | C | G | 31 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0105 others(28): Show |
36 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.409-355G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540934 | |||||||
chr14:100541007 | C | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0001t0001g0077 |
3 | HG00673.hp1 NA18989.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.409-428G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541007 | |||||||
chr14:100541014 | A | G | 31 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0105 others(28): Show |
36 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.409-435T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541014 | |||||||
chr14:100541037 | C | T | 1 | a0001c0004t0002g0203 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.409-458G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541037 | |||||||
chr14:100541049 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409-470C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541049 | |||||||
chr14:100541106 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.409-527C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541106 | |||||||
chr14:100541111 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.409-532C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541111 | |||||||
chr14:100541194 | C | T | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-615G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541194 | |||||||
chr14:100541232 | T | C | 1 | a0001c0003t0001g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.409-653A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541232 | |||||||
chr14:100541267 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.409-688G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541267 | |||||||
chr14:100541326 | A | G | 2 | a0001c0002t0001g0083 a0001c0002t0001g0166 |
2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.409-747T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541326 | |||||||
chr14:100541454 | C | T | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-875G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541454 | |||||||
chr14:100541518 | C | T | 34 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0105 others(31): Show |
39 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.409-939G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541518 | |||||||
chr14:100541574 | C | T | 2 | a0001c0002t0001g0125 a0001c0002t0001g0146 |
2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.409-995G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541574 | |||||||
chr14:100541607 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-1028T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541607 | |||||||
chr14:100541702 | G | C | 2 | a0001c0001t0001g0113 a0001c0009t0001g0102 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.409-1123C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541702 | |||||||
chr14:100541848 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1269G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541848 | |||||||
chr14:100541866 | G | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1287C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541866 | |||||||
chr14:100541937 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409-1358C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541937 | |||||||
chr14:100542139 | C | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1560G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542139 | |||||||
chr14:100542217 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1638G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542217 | |||||||
chr14:100542315 | G | T | 4 | a0001c0004t0001g0241 a0001c0004t0002g0006 a0001c0004t0002g0203 others(1): Show |
6 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+1543C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542315 | |||||||
chr14:100542446 | G | A | 1 | a0001c0005t0002g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.408+1412C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542446 | |||||||
chr14:100542481 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.408+1377G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542481 | |||||||
chr14:100542482 | G | A | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+1376C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542482 | |||||||
chr14:100542510 | C | T | 3 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0016t0001g0182 |
3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.408+1348G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542510 | |||||||
chr14:100542528 | G | A | 34 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0105 others(31): Show |
39 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.408+1330C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542528 | |||||||
chr14:100542596 | G | A | 1 | a0001c0001t0013g0086 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.408+1262C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542596 | |||||||
chr14:100542632 | GC | G | 4 | a0001c0005t0001g0106 a0001c0005t0001g0233 a0001c0005t0010g0107 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+1225delG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542632 | |||||||
chr14:100542790 | T | G | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+1068A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542790 | |||||||
chr14:100542832 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+1026G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542832 | |||||||
chr14:100542949 | T | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0120 |
3 | HG00741.hp2 HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.408+909A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542949 | |||||||
chr14:100542995 | GCTGGGCG others(3): Show |
G | 3 | a0001c0004t0002g0006 a0001c0004t0002g0203 a0001c0004t0017g0290 |
5 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+853_408+862del others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542995 | |||||||
chr14:100543043 | A | G | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+815T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543043 | |||||||
chr14:100543141 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+717G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543141 | |||||||
chr14:100543162 | G | GA | 4 | a0001c0005t0001g0106 a0001c0005t0001g0233 a0001c0005t0010g0107 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+695dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543162 | |||||||
chr14:100543292 | GTGTTTTT others(5): Show |
G | 1 | a0001c0006t0001g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+554_408+565del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543292 | |||||||
chr14:100543295 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0001g0090 others(3): Show |
7 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+563A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543295 | |||||||
chr14:100543306 | G | GT | 23 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0237 others(20): Show |
27 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.408+551dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543306 | |||||||
chr14:100543306 | G | T | 1 | a0001c0002t0012g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.408+552C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543306 | |||||||
chr14:100543311 | T | G | 1 | a0001c0005t0002g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.408+547A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543311 | |||||||
chr14:100543318 | G | T | 1 | a0001c0006t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+540C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543318 | |||||||
chr14:100543530 | A | G | 5 | a0001c0004t0001g0241 a0001c0005t0001g0106 a0001c0005t0001g0233 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+328T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543530 | |||||||
chr14:100543618 | G | T | 8 | a0001c0001t0001g0214 a0001c0005t0002g0022 a0001c0005t0002g0109 others(5): Show |
9 | HG00733.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+240C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543618 | |||||||
chr14:100543834 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.408+24C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543834 | |||||||
chr14:100543978 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.301-13G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100543978 | |||||||
chr14:100544027 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.301-62C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544027 | |||||||
chr14:100544042 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-77G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544042 | |||||||
chr14:100544082 | A | T | 7 | a0001c0003t0001g0007 a0001c0003t0001g0205 a0001c0003t0001g0213 others(4): Show |
9 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-117T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544082 | |||||||
chr14:100544393 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(136): Show |
165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.301-428A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544393 | |||||||
chr14:100544439 | G | C | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-474C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544439 | |||||||
chr14:100544478 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0169 |
2 | HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.301-513G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544478 | |||||||
chr14:100544522 | G | A | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+478C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544522 | |||||||
chr14:100544665 | T | A | 1 | a0001c0006t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.300+335A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544665 | |||||||
chr14:100544671 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.300+329G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544671 | |||||||
chr14:100544689 | C | T | 14 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0108 others(11): Show |
17 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.300+311G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544689 | |||||||
chr14:100544835 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0176 |
2 | NA19067.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.300+165G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544835 | |||||||
chr14:100544872 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.300+128T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544872 | |||||||
chr14:100544982 | G | A | 8 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(5): Show |
8 | HG01099.hp2 HG02922.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+18C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544982 | |||||||
chr14:100545439 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-373G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545439 | |||||||
chr14:100545607 | G | A | 1 | a0001c0006t0001g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.234-541C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545607 | |||||||
chr14:100545863 | C | T | 3 | a0001c0002t0001g0094 a0001c0002t0001g0140 a0001c0002t0001g0161 |
3 | HG00099.hp2 HG01978.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.233+638G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545863 | |||||||
chr14:100545879 | C | T | 1 | a0001c0002t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+622G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545879 | |||||||
chr14:100546082 | G | A | 2 | a0001c0006t0001g0198 a0001c0006t0001g0272 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.233+419C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546082 | |||||||
chr14:100546117 | C | G | 4 | a0001c0005t0001g0106 a0001c0005t0001g0233 a0001c0005t0010g0107 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+384G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546117 | |||||||
chr14:100546192 | C | A | 1 | a0001c0002t0001g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.233+309G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546192 | |||||||
chr14:100546272 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(20): Show |
27 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.233+229C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546272 | |||||||
chr14:100546276 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
228 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.233+225T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546276 | |||||||
chr14:100546290 | G | A | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233+211C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546290 | |||||||
chr14:100546333 | T | TGCCCCGC others(44): Show |
2 | a0001c0002t0001g0083 a0001c0002t0001g0181 |
2 | HG00140.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.233+167_233+168ins others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546333 | |||||||
chr14:100546333 | T | TGCCCCGC others(61): Show |
2 | a0001c0002t0001g0217 a0001c0004t0003g0129 |
2 | NA18969.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.233+167_233+168ins others(68): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546333 | |||||||
chr14:100546339 | A | ACCCCGGC others(10): Show |
17 | a0001c0002t0001g0029 a0001c0002t0001g0047 a0001c0002t0001g0118 others(14): Show |
17 | HG00558.hp2 HG01517.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.233+145_233+161dup others(17): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(45): Show |
1 | a0001c0002t0001g0035 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.233+161_233+162ins others(52): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(79): Show |
1 | a0001c0002t0001g0173 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.233+161_233+162ins others(86): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(96): Show |
1 | a0001c0002t0001g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.233+161_233+162ins others(103): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(27): Show |
19 | a0001c0001t0001g0164 a0001c0002t0001g0033 a0001c0002t0001g0072 others(16): Show |
19 | HG00408.hp2 HG00423.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.233+128_233+161dup others(34): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(44): Show |
19 | a0001c0002t0001g0026 a0001c0002t0001g0043 a0001c0002t0001g0057 others(16): Show |
19 | HG00438.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.233+111_233+161dup others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(61): Show |
8 | a0001c0002t0001g0138 a0001c0002t0001g0146 a0001c0002t0001g0154 others(5): Show |
9 | HG01243.hp1 HG02683.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+94_233+161dupC others(67): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(78): Show |
5 | a0001c0002t0001g0094 a0001c0002t0001g0145 a0001c0002t0001g0153 others(2): Show |
5 | HG00099.hp2 NA18942.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+77_233+161dupC others(84): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(95): Show |
3 | a0001c0002t0001g0096 a0001c0002t0001g0251 a0001c0004t0003g0100 |
3 | HG02080.hp1 NA18962.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.233+60_233+161dupC others(101): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(112): Show |
1 | a0001c0002t0001g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.233+43_233+161dupC others(118): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | ACCCCGGC others(129): Show |
1 | a0001c0002t0001g0131 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.233+26_233+161dupC others(135): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | A | G | 4 | a0001c0002t0001g0083 a0001c0002t0001g0181 a0001c0002t0001g0217 others(1): Show |
4 | HG00140.hp2 NA18969.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+162T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(10): Show |
A | 11 | a0001c0002t0001g0137 a0001c0002t0001g0152 a0001c0002t0001g0185 others(8): Show |
11 | HG01891.hp1 HG02647.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+145_233+161del others(17): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(27): Show |
A | 21 | a0001c0001t0001g0113 a0001c0001t0001g0192 a0001c0002t0001g0136 others(18): Show |
23 | HG00642.hp1 HG00733.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+128_233+161del others(34): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(44): Show |
A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0020 others(28): Show |
38 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+111_233+161del others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(61): Show |
A | 32 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0031 others(29): Show |
33 | HG01070.hp1 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.233+94_233+161delC others(67): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(78): Show |
A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0005t0001g0224 others(3): Show |
7 | HG00544.hp1 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+77_233+161delC others(84): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(95): Show |
A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
106 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.233+60_233+161del | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546339 | ACCCCGGC others(112): Show |
A | 7 | a0001c0001t0001g0214 a0001c0003t0001g0246 a0001c0004t0001g0241 others(4): Show |
7 | HG00733.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+43_233+161del | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | |||||||
chr14:100546391 | C | G | 2 | a0001c0003t0001g0114 a0001c0003t0005g0282 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.233+110G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546391 | |||||||
chr14:100546408 | C | G | 11 | a0001c0001t0001g0113 a0001c0001t0001g0192 a0001c0001t0001g0208 others(8): Show |
11 | HG00733.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+93G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546408 | |||||||
chr14:100546425 | C | G | 37 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0113 others(34): Show |
40 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.233+76G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546425 | |||||||
chr14:100546442 | C | G | 82 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(79): Show |
90 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.233+59G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546442 | |||||||
chr14:100546459 | C | G | 97 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(94): Show |
109 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+42G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546459 | |||||||
chr14:100546476 | C | CCCCGGCC others(10): Show |
1 | a0001c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.233+24_233+25insCC others(15): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546476 | |||||||
chr14:100546476 | C | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
219 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.233+25G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546476 | |||||||
chr14:100546689 | G | A | 3 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0016t0001g0182 |
3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-27C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546689 | |||||||
chr14:100546763 | G | GGC | 7 | a0001c0001t0001g0012 a0001c0001t0001g0090 a0001c0001t0001g0099 others(4): Show |
8 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-103_72-102dupGC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | |||||||
chr14:100546763 | GGC | G | 15 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0054 others(12): Show |
15 | HG00438.hp1 HG01099.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-103_72-102delGC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | |||||||
chr14:100546763 | GGCGC | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0214 a0001c0001t0001g0226 others(1): Show |
4 | HG00621.hp2 HG00733.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-105_72-102delGC others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | |||||||
chr14:100546767 | C | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-105G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546767 | |||||||
chr14:100546774 | GCGCGCGC others(3): Show |
G | 15 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0108 others(12): Show |
18 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-122_72-113delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | |||||||
chr14:100546774 | GCGCGCGC others(9): Show |
G | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-128_72-113delTG others(14): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | |||||||
chr14:100546774 | GCGCGCGC others(11): Show |
G | 5 | a0001c0005t0001g0106 a0001c0005t0001g0233 a0001c0005t0010g0107 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-130_72-113delTG others(16): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | |||||||
chr14:100546776 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72-114C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546776 | G | GCA | 4 | a0001c0001t0001g0139 a0001c0001t0001g0212 a0001c0001t0001g0227 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-115_72-114insTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546776 | G | GCACA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG02258.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-115_72-114insTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546776 | GCGCGCAC others(1): Show |
G | 7 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0003t0005g0282 others(4): Show |
8 | HG01978.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-122_72-115delTG others(6): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546776 | GCGCGCAC others(3): Show |
G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
9 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-124_72-115delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546776 | GCGCGCAC others(5): Show |
G | 2 | a0001c0003t0001g0260 a0001c0008t0001g0209 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72-126_72-115delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | |||||||
chr14:100546778 | G | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(22): Show |
27 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.72-116C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546778 | GCGCA | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
71 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.72-120_72-117delTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546778 | GCGCACA | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(13): Show |
21 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.72-122_72-117delTG others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546778 | GCGCACAC others(3): Show |
G | 1 | a0001c0003t0001g0246 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.72-126_72-117delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546778 | GCGCACAC others(5): Show |
G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.72-128_72-117delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546778 | GCGCACAC others(7): Show |
G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG01099.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-130_72-117delTG others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | |||||||
chr14:100546780 | G | A | 39 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(36): Show |
44 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.72-118C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | G | GCA | 13 | a0001c0002t0001g0014 a0001c0002t0001g0059 a0001c0002t0001g0085 others(10): Show |
13 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-120_72-119dupTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | GCA | G | 48 | a0001c0001t0001g0164 a0001c0002t0001g0026 a0001c0002t0001g0029 others(45): Show |
48 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.72-120_72-119delTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | GCACA | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0133 others(4): Show |
7 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-122_72-119delTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | GCACACA | G | 4 | a0001c0001t0001g0001 a0001c0002t0001g0125 a0001c0002t0001g0146 others(1): Show |
4 | HG00099.hp1 HG02135.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-124_72-119delTG others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | GCACACAC others(5): Show |
G | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-130_72-119delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546780 | GCACACAC others(7): Show |
G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0202 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.72-132_72-119delTG others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | |||||||
chr14:100546782 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.72-120T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546782 | |||||||
chr14:100546784 | A | G | 1 | a0001c0002t0012g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.72-122T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546784 | |||||||
chr14:100546786 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-124T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546786 | |||||||
chr14:100546790 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-128T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546790 | |||||||
chr14:100546794 | A | G | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-132T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546794 | |||||||
chr14:100546806 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.72-144T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546806 | |||||||
chr14:100546810 | A | T | 16 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0108 others(13): Show |
19 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-148T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546810 | |||||||
chr14:100546812 | ACTCACAC others(4): Show |
A | 1 | a0001c0008t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72-161_72-151delGT others(9): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546812 | |||||||
chr14:100546814 | T | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(35): Show |
45 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.72-152A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546814 | |||||||
chr14:100546823 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.72-161G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546823 | |||||||
chr14:100546837 | C | A | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-175G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546837 | |||||||
chr14:100546852 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.72-190A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546852 | |||||||
chr14:100546885 | C | T | 4 | a0001c0005t0001g0106 a0001c0005t0001g0233 a0001c0005t0010g0107 others(1): Show |
4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-223G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546885 | |||||||
chr14:100547059 | C | G | 10 | a0001c0003t0001g0013 a0001c0003t0001g0108 a0001c0003t0001g0110 others(7): Show |
11 | HG02109.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-397G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547059 | |||||||
chr14:100547343 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0250 |
2 | HG00609.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.72-681G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547343 | |||||||
chr14:100547492 | T | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(49): Show |
60 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.72-830A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547492 | |||||||
chr14:100547653 | G | A | 2 | a0001c0006t0001g0198 a0001c0006t0001g0272 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72-991C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547653 | |||||||
chr14:100547704 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.72-1042C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547704 | |||||||
chr14:100547712 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-1050G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547712 | |||||||
chr14:100547796 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
16 | HG00544.hp2 HG00558.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-1134A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547796 | |||||||
chr14:100547880 | C | T | 1 | a0001c0002t0001g0162 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.72-1218G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547880 | |||||||
chr14:100547950 | A | G | 4 | a0001c0001t0001g0208 a0001c0003t0001g0260 a0001c0008t0001g0200 others(1): Show |
4 | HG02055.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1288T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547950 | |||||||
chr14:100548081 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
215 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.72-1419C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548081 | |||||||
chr14:100548172 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.72-1510C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548172 | |||||||
chr14:100548255 | A | T | 9 | a0001c0001t0001g0214 a0001c0005t0001g0224 a0001c0005t0002g0022 others(6): Show |
10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-1593T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548255 | |||||||
chr14:100548296 | A | AG | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
214 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.72-1635_72-1634ins others(1): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548296 | |||||||
chr14:100548364 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0079 a0001c0001t0001g0087 |
6 | HG00639.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-1702C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548364 | |||||||
chr14:100548381 | T | C | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-1719A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548381 | |||||||
chr14:100548492 | C | T | 1 | a0001c0006t0001g0272 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72-1830G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548492 | |||||||
chr14:100548539 | C | G | 8 | a0001c0003t0001g0013 a0001c0003t0001g0108 a0001c0003t0001g0110 others(5): Show |
9 | HG02109.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-1877G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548539 | |||||||
chr14:100548692 | G | A | 1 | a0001c0003t0001g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-2030C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548692 | |||||||
chr14:100548734 | A | G | 3 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0016t0001g0182 |
3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-2072T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548734 | |||||||
chr14:100548781 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.72-2119G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548781 | |||||||
chr14:100548824 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2162G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548824 | |||||||
chr14:100548853 | C | T | 3 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0016t0001g0182 |
3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-2191G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548853 | |||||||
chr14:100548907 | C | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0271 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.72-2245G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548907 | |||||||
chr14:100549043 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
170 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.72-2381A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549043 | |||||||
chr14:100549044 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72-2382G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549044 | |||||||
chr14:100549099 | G | A | 9 | a0001c0001t0001g0208 a0001c0003t0001g0105 a0001c0003t0001g0260 others(6): Show |
11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-2437C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549099 | |||||||
chr14:100549106 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.72-2444C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549106 | |||||||
chr14:100549128 | A | C | 7 | a0001c0005t0002g0022 a0001c0005t0002g0109 a0001c0005t0002g0218 others(4): Show |
8 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-2466T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549128 | |||||||
chr14:100549196 | C | T | 2 | a0001c0002t0001g0035 a0001c0002t0001g0173 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.72-2534G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549196 | |||||||
chr14:100549197 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.72-2535C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549197 | |||||||
chr14:100549292 | G | A | 14 | a0001c0003t0001g0231 a0001c0003t0001g0246 a0001c0004t0001g0021 others(11): Show |
15 | HG00544.hp1 HG02056.hp2 NA18964.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-2630C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549292 | |||||||
chr14:100549526 | A | G | 1 | a0001c0001t0014g0248 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.72-2864T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549526 | |||||||
chr14:100549594 | G | C | 2 | a0001c0002t0001g0083 a0001c0002t0001g0166 |
2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.72-2932C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549594 | |||||||
chr14:100549605 | C | G | 3 | a0001c0005t0002g0218 a0001c0005t0002g0219 a0001c0005t0002g0254 |
3 | HG01891.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.72-2943G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549605 | |||||||
chr14:100549847 | A | G | 2 | a0001c0001t0001g0113 a0001c0009t0001g0102 |
2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.72-3185T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549847 | |||||||
chr14:100549853 | G | A | 39 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(36): Show |
42 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.72-3191C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549853 | |||||||
chr14:100549902 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.72-3240T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549902 | |||||||
chr14:100549906 | A | G | 1 | a0001c0005t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-3244T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549906 | |||||||
chr14:100549970 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
101 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.72-3308G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549970 | |||||||
chr14:100550037 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.72-3375C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550037 | |||||||
chr14:100550163 | G | A | 2 | a0001c0003t0001g0105 a0001c0003t0001g0276 |
2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.72-3501C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550163 | |||||||
chr14:100550204 | C | T | 1 | a0001c0003t0001g0276 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72-3542G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550204 | |||||||
chr14:100550230 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
228 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.72-3568T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550230 | |||||||
chr14:100550385 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.72-3723G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550385 | |||||||
chr14:100550483 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72-3821G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550483 | |||||||
chr14:100550487 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.72-3825T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550487 | |||||||
chr14:100550550 | G | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0116 others(4): Show |
8 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-3888C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550550 | |||||||
chr14:100550586 | A | G | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-3924T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550586 | |||||||
chr14:100550659 | C | CTTG | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.72-4000_72-3998dup others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550659 | |||||||
chr14:100550763 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72-4101G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550763 | |||||||
chr14:100550766 | C | G | 44 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(41): Show |
49 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.72-4104G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550766 | |||||||
chr14:100550855 | G | A | 1 | a0001c0003t0001g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.72-4193C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550855 | |||||||
chr14:100550894 | G | A | 1 | a0001c0005t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-4232C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550894 | |||||||
chr14:100550934 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.72-4272C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550934 | |||||||
chr14:100551153 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(19): Show |
25 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.72-4491G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551153 | |||||||
chr14:100551229 | G | A | 3 | a0001c0002t0001g0026 a0001c0002t0001g0043 a0001c0002t0001g0128 |
3 | NA18969.hp1 NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.72-4567C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551229 | |||||||
chr14:100551344 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.72-4682G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551344 | |||||||
chr14:100551345 | G | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG02258.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4683C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551345 | |||||||
chr14:100551484 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.72-4822C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551484 | |||||||
chr14:100551709 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.72-5047T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551709 | |||||||
chr14:100551734 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
143 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.72-5072T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551734 | |||||||
chr14:100552002 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5340G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552002 | |||||||
chr14:100552051 | C | T | 4 | a0001c0003t0001g0215 a0001c0004t0002g0006 a0001c0004t0002g0203 others(1): Show |
6 | HG02486.hp2 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-5389G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552051 | |||||||
chr14:100552159 | G | A | 5 | a0001c0001t0001g0113 a0001c0003t0001g0110 a0001c0003t0001g0111 others(2): Show |
5 | HG02809.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5497C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552159 | |||||||
chr14:100552320 | T | G | 1 | a0001c0003t0001g0278 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.72-5658A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552320 | |||||||
chr14:100552491 | A | C | 4 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(1): Show |
4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-5829T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552491 | |||||||
chr14:100552526 | C | T | 5 | a0001c0003t0001g0105 a0001c0003t0001g0242 a0001c0003t0001g0243 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5864G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552526 | |||||||
chr14:100552600 | G | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0232 |
2 | HG01070.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.72-5938C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552600 | |||||||
chr14:100552737 | G | A | 1 | a0001c0003t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72-6075C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552737 | |||||||
chr14:100552752 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-6090G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552752 | |||||||
chr14:100552959 | G | T | 1 | a0001c0013t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72-6297C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552959 | |||||||
chr14:100553092 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(18): Show |
24 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-6430G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553092 | |||||||
chr14:100553108 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-6446G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553108 | |||||||
chr14:100553631 | G | A | 1 | a0003c0015t0001g0132 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72-6969C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553631 | |||||||
chr14:100553895 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.72-7233G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553895 | |||||||
chr14:100554114 | C | T | 4 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(1): Show |
4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-7452G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554114 | |||||||
chr14:100554182 | G | A | 9 | a0001c0003t0001g0105 a0001c0003t0001g0215 a0001c0003t0001g0276 others(6): Show |
11 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-7520C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554182 | |||||||
chr14:100554322 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7660C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554322 | |||||||
chr14:100554463 | C | T | 50 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(47): Show |
54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.72-7801G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554463 | |||||||
chr14:100554532 | C | T | 13 | a0001c0003t0001g0105 a0001c0003t0001g0215 a0001c0003t0001g0240 others(10): Show |
15 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-7870G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554532 | |||||||
chr14:100554732 | C | A | 10 | a0001c0001t0001g0116 a0001c0001t0001g0214 a0001c0001t0001g0216 others(7): Show |
10 | HG00733.hp2 HG01884.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-8070G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554732 | |||||||
chr14:100554881 | C | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.72-8219G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554881 | |||||||
chr14:100554908 | GGCCTTCG others(6): Show |
G | 10 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(7): Show |
11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-8259_72-8247del others(13): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554908 | |||||||
chr14:100555072 | C | T | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-8410G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555072 | |||||||
chr14:100555221 | C | T | 53 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(50): Show |
57 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.72-8559G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555221 | |||||||
chr14:100555520 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0062 |
2 | HG01952.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.72-8858G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555520 | |||||||
chr14:100555679 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.72-9017C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555679 | |||||||
chr14:100555713 | C | T | 3 | a0001c0004t0003g0264 a0001c0004t0003g0265 a0001c0004t0003g0266 |
3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.72-9051G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555713 | |||||||
chr14:100555879 | A | G | 1 | a0001c0002t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.72-9217T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555879 | |||||||
chr14:100555940 | T | G | 4 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(1): Show |
4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-9278A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555940 | |||||||
chr14:100556004 | T | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
9 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-9342A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556004 | |||||||
chr14:100556238 | C | G | 7 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0216 others(4): Show |
7 | HG00733.hp2 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-9576G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556238 | |||||||
chr14:100556327 | G | A | 12 | a0001c0002t0001g0029 a0001c0002t0001g0115 a0001c0002t0001g0119 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-9665C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556327 | |||||||
chr14:100556335 | G | GC | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(53): Show |
60 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.72-9674dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556335 | |||||||
chr14:100556338 | C | G | 10 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(7): Show |
11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-9676G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556338 | |||||||
chr14:100556344 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72-9682G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556344 | |||||||
chr14:100556505 | G | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0116 others(3): Show |
7 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-9843C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556505 | |||||||
chr14:100556857 | C | T | 5 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10195G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556857 | |||||||
chr14:100556902 | C | A | 1 | a0001c0003t0001g0246 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.72-10240G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556902 | |||||||
chr14:100556942 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.72-10280G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556942 | |||||||
chr14:100556971 | C | T | 1 | a0001c0005t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-10309G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556971 | |||||||
chr14:100557055 | TCTGCCGG others(63): Show |
T | 60 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(57): Show |
65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.72-10463_72-10394d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557055 | |||||||
chr14:100557099 | G | C | 19 | a0001c0001t0001g0116 a0001c0001t0001g0208 a0001c0001t0001g0214 others(16): Show |
20 | HG00733.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.72-10437C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557099 | |||||||
chr14:100557111 | G | GTCCCAGC others(63): Show |
1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-10519_72-10450d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557111 | |||||||
chr14:100557125 | CCTGCCGG others(63): Show |
C | 1 | a0001c0001t0001g0015 | 2 | HG00597.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.72-10533_72-10464d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557125 | |||||||
chr14:100557129 | C | T | 2 | a0001c0003t0001g0278 a0001c0005t0010g0107 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.72-10467G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557129 | |||||||
chr14:100557147 | A | C | 3 | a0001c0004t0003g0264 a0001c0004t0003g0265 a0001c0004t0003g0266 |
3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.72-10485T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557147 | |||||||
chr14:100557181 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.72-10519T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557181 | |||||||
chr14:100557195 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0036 |
3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-10533A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557195 | |||||||
chr14:100557201 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0036 |
3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-10539T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557201 | |||||||
chr14:100557273 | G | A | 4 | a0001c0001t0001g0116 a0001c0003t0001g0278 a0001c0005t0001g0224 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-10611C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557273 | |||||||
chr14:100557286 | G | A | 4 | a0001c0001t0001g0116 a0001c0003t0001g0278 a0001c0005t0001g0224 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-10624C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557286 | |||||||
chr14:100557287 | G | A | 4 | a0001c0001t0001g0116 a0001c0003t0001g0278 a0001c0005t0001g0224 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+10624C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557287 | |||||||
chr14:100557330 | C | T | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+10581G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557330 | |||||||
chr14:100557369 | C | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
67 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.71+10542G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557369 | |||||||
chr14:100557458 | C | T | 57 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(54): Show |
62 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.71+10453G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557458 | |||||||
chr14:100557592 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+10319T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557592 | |||||||
chr14:100557904 | C | A | 13 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(10): Show |
15 | HG00558.hp2 HG01891.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.71+10007G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557904 | |||||||
chr14:100557956 | G | C | 2 | a0001c0003t0001g0278 a0001c0005t0010g0107 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.71+9955C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557956 | |||||||
chr14:100557960 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 |
5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+9951G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557960 | |||||||
chr14:100558075 | C | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0003t0001g0215 |
3 | HG00733.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.71+9836G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558075 | |||||||
chr14:100558191 | GAA | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.71+9718_71+9719del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558191 | |||||||
chr14:100558205 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
7 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+9706A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558205 | |||||||
chr14:100558387 | C | G | 3 | a0001c0002t0001g0136 a0001c0002t0001g0137 a0001c0002t0001g0152 |
3 | NA18971.hp1 NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.71+9524G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558387 | |||||||
chr14:100558468 | C | T | 1 | a0001c0004t0001g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+9443G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558468 | |||||||
chr14:100558608 | G | C | 5 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+9303C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558608 | |||||||
chr14:100558844 | C | T | 5 | a0001c0001t0001g0116 a0001c0003t0001g0278 a0001c0004t0001g0241 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+9067G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558844 | |||||||
chr14:100558921 | A | G | 11 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(8): Show |
12 | HG02056.hp2 HG02622.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+8990T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558921 | |||||||
chr14:100558945 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0192 |
2 | HG00733.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.71+8966G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558945 | |||||||
chr14:100559190 | G | A | 10 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(7): Show |
11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+8721C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559190 | |||||||
chr14:100559210 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+8701G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559210 | |||||||
chr14:100559329 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.71+8582G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559329 | |||||||
chr14:100559381 | T | A | 17 | a0001c0002t0001g0115 a0001c0002t0001g0119 a0001c0002t0001g0172 others(14): Show |
19 | HG00558.hp2 HG01891.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.71+8530A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559381 | |||||||
chr14:100559482 | C | T | 1 | a0001c0002t0001g0149 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.71+8429G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559482 | |||||||
chr14:100559563 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+8348G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559563 | |||||||
chr14:100559711 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.71+8200G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559711 | |||||||
chr14:100559721 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+8190T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559721 | |||||||
chr14:100559799 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.71+8112G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559799 | |||||||
chr14:100559811 | G | A | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.71+8100C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559811 | |||||||
chr14:100559962 | A | G | 74 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(71): Show |
80 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.71+7949T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559962 | |||||||
chr14:100559974 | G | A | 2 | a0001c0002t0006g0286 a0001c0002t0006g0287 |
2 | HG02735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.71+7937C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559974 | |||||||
chr14:100560017 | ATC | A | 10 | a0001c0004t0001g0021 a0001c0004t0001g0268 a0001c0004t0003g0100 others(7): Show |
11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+7892_71+7893del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560017 | |||||||
chr14:100560031 | C | T | 1 | a0001c0003t0001g0278 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.71+7880G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560031 | |||||||
chr14:100560259 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
84 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+7652G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560259 | |||||||
chr14:100560362 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.71+7549G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560362 | |||||||
chr14:100560453 | C | T | 3 | a0001c0001t0001g0227 a0001c0003t0001g0007 a0001c0003t0001g0205 |
5 | HG02451.hp1 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+7458G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560453 | |||||||
chr14:100560454 | G | A | 3 | a0001c0003t0001g0204 a0001c0003t0001g0206 a0001c0003t0001g0210 |
3 | HG02280.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.71+7457C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560454 | |||||||
chr14:100560548 | C | T | 3 | a0001c0004t0003g0264 a0001c0004t0003g0265 a0001c0004t0003g0266 |
3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.71+7363G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560548 | |||||||
chr14:100560688 | C | T | 6 | a0001c0001t0001g0070 a0001c0002t0001g0029 a0001c0003t0001g0231 others(3): Show |
6 | HG00544.hp1 HG02698.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+7223G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560688 | |||||||
chr14:100560796 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.71+7115A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560796 | |||||||
chr14:100560820 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(25): Show |
32 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+7091G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560820 | |||||||
chr14:100560964 | C | T | 7 | a0001c0003t0001g0278 a0001c0003t0005g0282 a0001c0003t0006g0288 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+6947G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560964 | |||||||
chr14:100560988 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.71+6923C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560988 | |||||||
chr14:100561001 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.71+6910A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561001 | |||||||
chr14:100561036 | TG | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.71+6874delC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561036 | |||||||
chr14:100561064 | G | A | 1 | a0001c0002t0004g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.71+6847C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561064 | |||||||
chr14:100561104 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+6807C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561104 | |||||||
chr14:100561111 | C | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
69 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.71+6800G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561111 | |||||||
chr14:100561195 | C | T | 2 | a0001c0001t0001g0177 a0003c0015t0001g0132 |
2 | HG01169.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.71+6716G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561195 | |||||||
chr14:100561423 | C | G | 1 | a0001c0002t0005g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.71+6488G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561423 | |||||||
chr14:100561454 | G | A | 6 | a0001c0001t0001g0113 a0001c0003t0001g0110 a0001c0003t0001g0111 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+6457C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561454 | |||||||
chr14:100561497 | C | G | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+6414G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561497 | |||||||
chr14:100561557 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
121 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.71+6354A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561557 | |||||||
chr14:100561558 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
98 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.71+6353C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561558 | |||||||
chr14:100561558 | G | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | NA19012.hp1 NA19081.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.71+6353C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561558 | |||||||
chr14:100561583 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0142 |
3 | HG01943.hp1 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.71+6328A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561583 | |||||||
chr14:100561614 | G | A | 1 | a0001c0003t0005g0282 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71+6297C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561614 | |||||||
chr14:100561669 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(96): Show |
122 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.71+6242A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561669 | |||||||
chr14:100561716 | G | GA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
117 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.71+6194dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561716 | |||||||
chr14:100561716 | G | GAA | 8 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0002t0006g0286 others(5): Show |
9 | HG02055.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+6193_71+6194dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561716 | |||||||
chr14:100561733 | G | A | 1 | a0001c0003t0001g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71+6178C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561733 | |||||||
chr14:100561891 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.71+6020T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561891 | |||||||
chr14:100562062 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.71+5849T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562062 | |||||||
chr14:100562079 | C | G | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+5832G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562079 | |||||||
chr14:100562081 | A | G | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+5830T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562081 | |||||||
chr14:100562238 | G | A | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+5673C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562238 | |||||||
chr14:100562283 | C | T | 1 | a0001c0004t0003g0270 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.71+5628G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562283 | |||||||
chr14:100562481 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.71+5430C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562481 | |||||||
chr14:100562503 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.71+5408A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562503 | |||||||
chr14:100562512 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0003t0001g0215 |
3 | HG00733.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.71+5399C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562512 | |||||||
chr14:100562562 | C | G | 20 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
22 | HG01099.hp2 HG02055.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+5349G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562562 | |||||||
chr14:100562587 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+5324C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562587 | |||||||
chr14:100562637 | A | G | 1 | a0001c0002t0001g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.71+5274T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562637 | |||||||
chr14:100562664 | C | G | 6 | a0001c0001t0001g0227 a0001c0003t0001g0240 a0001c0003t0001g0242 others(3): Show |
6 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+5247G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562664 | |||||||
chr14:100562694 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.71+5217C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562694 | |||||||
chr14:100562707 | G | T | 1 | a0001c0003t0001g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71+5204C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562707 | |||||||
chr14:100562812 | G | A | 7 | a0001c0003t0001g0278 a0001c0003t0005g0282 a0001c0003t0006g0288 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+5099C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562812 | |||||||
chr14:100562866 | G | A | 91 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(88): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.71+5045C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562866 | |||||||
chr14:100562963 | C | CA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.71+4947dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562963 | |||||||
chr14:100562987 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.71+4924T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562987 | |||||||
chr14:100562998 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.71+4913C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562998 | |||||||
chr14:100563412 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.71+4499T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563412 | |||||||
chr14:100563522 | G | A | 6 | a0001c0001t0001g0113 a0001c0003t0001g0110 a0001c0003t0001g0111 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+4389C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563522 | |||||||
chr14:100563544 | A | G | 28 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(25): Show |
30 | HG01099.hp2 HG01891.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.71+4367T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563544 | |||||||
chr14:100563547 | C | T | 5 | a0001c0003t0005g0282 a0001c0003t0006g0288 a0001c0003t0006g0289 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+4364G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563547 | |||||||
chr14:100563610 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.71+4301G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563610 | |||||||
chr14:100563672 | A | AC | 4 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG00423.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4238dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563672 | |||||||
chr14:100563673 | C | T | 2 | a0001c0001t0001g0123 a0001c0002t0001g0120 |
2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.71+4238G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563673 | |||||||
chr14:100563694 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0001t0001g0192 |
3 | HG00733.hp1 HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.71+4217G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563694 | |||||||
chr14:100563849 | T | C | 1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71+4062A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563849 | |||||||
chr14:100563855 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+4056G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563855 | |||||||
chr14:100563860 | A | G | 35 | a0001c0001t0001g0113 a0001c0001t0001g0199 a0001c0001t0001g0201 others(32): Show |
37 | HG01099.hp2 HG01891.hp2 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.71+4051T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563860 | |||||||
chr14:100563895 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71+4016A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563895 | |||||||
chr14:100564064 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3847C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564064 | |||||||
chr14:100564121 | G | C | 1 | a0001c0002t0001g0163 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.71+3790C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564121 | |||||||
chr14:100564125 | G | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0176 a0001c0002t0001g0128 |
3 | NA18969.hp1 NA19067.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.71+3786C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564125 | |||||||
chr14:100564242 | G | A | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+3669C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564242 | |||||||
chr14:100564262 | G | C | 1 | a0001c0002t0001g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+3649C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564262 | |||||||
chr14:100564393 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71+3518T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564393 | |||||||
chr14:100564435 | A | T | 1 | a0001c0002t0001g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.71+3476T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564435 | |||||||
chr14:100564473 | G | A | 1 | a0001c0001t0013g0086 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71+3438C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564473 | |||||||
chr14:100564607 | T | C | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+3304A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564607 | |||||||
chr14:100564699 | C | T | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+3212G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564699 | |||||||
chr14:100564723 | G | A | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG02976.hp2 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3188C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564723 | |||||||
chr14:100564823 | C | T | 5 | a0001c0003t0005g0282 a0001c0003t0006g0288 a0001c0003t0006g0289 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+3088G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564823 | |||||||
chr14:100564971 | A | G | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+2940T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564971 | |||||||
chr14:100565373 | G | T | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+2538C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565373 | |||||||
chr14:100565529 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71+2382G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565529 | |||||||
chr14:100565659 | C | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0001g0256 others(1): Show |
5 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2252G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565659 | |||||||
chr14:100565696 | C | T | 1 | a0001c0001t0011g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71+2215G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565696 | |||||||
chr14:100565857 | AG | A | 5 | a0001c0003t0005g0282 a0001c0003t0006g0288 a0001c0003t0006g0289 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2053delC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565857 | |||||||
chr14:100565870 | T | C | 2 | a0001c0002t0001g0251 a0001c0002t0001g0277 |
2 | HG02080.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.71+2041A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565870 | |||||||
chr14:100565880 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+2031A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565880 | |||||||
chr14:100565986 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71+1925A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565986 | |||||||
chr14:100566041 | G | A | 2 | a0001c0004t0002g0006 a0001c0004t0002g0203 |
4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+1870C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566041 | |||||||
chr14:100566327 | C | T | 16 | a0001c0001t0001g0113 a0001c0003t0001g0013 a0001c0003t0001g0105 others(13): Show |
17 | HG02109.hp1 HG02258.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.71+1584G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566327 | |||||||
chr14:100566370 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+1541T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566370 | |||||||
chr14:100566494 | C | A | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+1417G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566494 | |||||||
chr14:100566519 | C | A | 4 | a0001c0001t0008g0221 a0001c0002t0001g0172 a0001c0002t0001g0225 others(1): Show |
4 | HG01884.hp1 HG02015.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+1392G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566519 | |||||||
chr14:100566521 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.71+1390G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566521 | |||||||
chr14:100566752 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
8 | HG01099.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+1159C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566752 | |||||||
chr14:100566951 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.71+960T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566951 | |||||||
chr14:100567083 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.71+828G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567083 | |||||||
chr14:100567098 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+813T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567098 | |||||||
chr14:100567281 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.71+630G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567281 | |||||||
chr14:100567498 | T | TGGGGGTG others(10): Show |
1 | a0001c0003t0001g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71+396_71+412dupGA others(15): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567498 | |||||||
chr14:100567573 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0236 |
3 | HG01106.hp1 HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.71+338C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567573 | |||||||
chr14:100567579 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.71+332G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567579 | |||||||
chr14:100567592 | G | C | 1 | a0001c0002t0012g0141 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.71+319C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567592 | |||||||
chr14:100567593 | G | T | 1 | a0001c0002t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71+318C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567593 | |||||||
chr14:100567627 | G | C | 1 | a0001c0003t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71+284C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567627 | |||||||
chr14:100567628 | G | A | 1 | a0001c0003t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71+283C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567628 | |||||||
chr14:100567636 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.71+275C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567636 | |||||||
chr14:100567734 | G | C | 2 | a0001c0002t0001g0035 a0001c0002t0001g0173 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.71+177C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567734 | |||||||
chr14:100567853 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0170 others(49): Show |
54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.71+58C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567853 | |||||||
chr14:100568073 | G | C | 2 | a0001c0004t0002g0006 a0001c0004t0002g0203 |
4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-134C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568073 | |||||||
chr14:100568082 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.43-143A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568082 | |||||||
chr14:100568088 | T | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-149A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568088 | |||||||
chr14:100568092 | G | A | 3 | a0001c0001t0001g0164 a0001c0002t0001g0097 a0001c0002t0001g0165 |
3 | HG01952.hp1 HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.43-153C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568092 | |||||||
chr14:100568115 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.43-176C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568115 | |||||||
chr14:100568621 | C | G | 1 | a0001c0002t0001g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.43-682G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568621 | |||||||
chr14:100568662 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-723G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568662 | |||||||
chr14:100568817 | C | T | 2 | a0001c0003t0001g0110 a0001c0003t0001g0111 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.43-878G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568817 | |||||||
chr14:100568925 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.43-986G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568925 | |||||||
chr14:100569065 | G | A | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(11): Show |
16 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-1126C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569065 | |||||||
chr14:100569165 | G | C | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG02145.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.43-1226C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569165 | |||||||
chr14:100569179 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.43-1240T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569179 | |||||||
chr14:100569209 | C | G | 80 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.43-1270G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569209 | |||||||
chr14:100569498 | C | G | 7 | a0001c0001t0001g0169 a0001c0001t0008g0134 a0001c0002t0001g0122 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-1559G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569498 | |||||||
chr14:100569581 | CCT | C | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-1644_43-1643del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569581 | |||||||
chr14:100569601 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43-1662G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569601 | |||||||
chr14:100569715 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.43-1776A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569715 | |||||||
chr14:100569737 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.43-1798G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569737 | |||||||
chr14:100569915 | A | G | 2 | a0001c0005t0002g0022 a0001c0005t0016g0285 |
3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.43-1976T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569915 | |||||||
chr14:100569931 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43-1992A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569931 | |||||||
chr14:100569932 | A | G | 2 | a0001c0003t0001g0013 a0001c0003t0001g0108 |
3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.43-1993T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569932 | |||||||
chr14:100569955 | C | G | 1 | a0001c0002t0001g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.43-2016G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569955 | |||||||
chr14:100570052 | G | A | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-2113C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570052 | |||||||
chr14:100570121 | C | A | 59 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(56): Show |
64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.43-2182G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570121 | |||||||
chr14:100570249 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.43-2310C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570249 | |||||||
chr14:100570303 | T | C | 15 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(12): Show |
16 | HG01099.hp2 HG02056.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-2364A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570303 | |||||||
chr14:100570360 | A | G | 7 | a0001c0001t0001g0113 a0001c0003t0001g0105 a0001c0003t0001g0110 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-2421T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570360 | |||||||
chr14:100570487 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.43-2548T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570487 | |||||||
chr14:100570495 | T | C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
23 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-2556A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570495 | |||||||
chr14:100570496 | GCGGCCCT others(1): Show |
G | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2565_43-2558del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570496 | |||||||
chr14:100570505 | T | A | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2566A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570505 | |||||||
chr14:100570507 | T | A | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2568A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570507 | |||||||
chr14:100570665 | A | G | 38 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(35): Show |
42 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.43-2726T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570665 | |||||||
chr14:100570678 | G | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.43-2739C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570678 | |||||||
chr14:100570687 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
143 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.43-2748T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570687 | |||||||
chr14:100570691 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
144 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.43-2752A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570691 | |||||||
chr14:100570791 | G | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0002t0001g0138 others(3): Show |
6 | HG00438.hp2 HG00609.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-2852C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570791 | |||||||
chr14:100570964 | A | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-3025T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570964 | |||||||
chr14:100571112 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.43-3173G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571112 | |||||||
chr14:100571136 | G | A | 2 | a0001c0001t0001g0087 a0001c0002t0001g0168 |
2 | HG01243.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.43-3197C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571136 | |||||||
chr14:100571262 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.43-3323T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571262 | |||||||
chr14:100571270 | C | G | 4 | a0001c0003t0001g0013 a0001c0003t0001g0108 a0001c0004t0002g0006 others(1): Show |
7 | HG02109.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-3331G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571270 | |||||||
chr14:100571284 | C | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-3345G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571284 | |||||||
chr14:100571312 | C | T | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-3373G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571312 | |||||||
chr14:100571346 | G | A | 2 | a0001c0003t0001g0278 a0001c0005t0010g0107 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-3407C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571346 | |||||||
chr14:100571372 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.43-3433G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571372 | |||||||
chr14:100571389 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.43-3450A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571389 | |||||||
chr14:100571405 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.43-3466C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571405 | |||||||
chr14:100571425 | C | G | 54 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.43-3486G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571425 | |||||||
chr14:100571448 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.43-3509C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571448 | |||||||
chr14:100571472 | C | G | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-3533G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571472 | |||||||
chr14:100571486 | A | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-3547T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571486 | |||||||
chr14:100571549 | T | C | 1 | a0001c0005t0002g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.43-3610A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571549 | |||||||
chr14:100571694 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43-3755A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571694 | |||||||
chr14:100571879 | C | G | 1 | a0001c0001t0011g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43-3940G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571879 | |||||||
chr14:100571916 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43-3977C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571916 | |||||||
chr14:100571992 | C | T | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-4053G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571992 | |||||||
chr14:100572102 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.43-4163G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572102 | |||||||
chr14:100572105 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.43-4166C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572105 | |||||||
chr14:100572123 | G | A | 42 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0194 others(39): Show |
44 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.43-4184C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572123 | |||||||
chr14:100572152 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG01884.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.43-4213C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572152 | |||||||
chr14:100572444 | A | G | 10 | a0001c0002t0001g0101 a0001c0004t0001g0021 a0001c0004t0001g0268 others(7): Show |
11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-4505T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572444 | |||||||
chr14:100572651 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
116 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.43-4712C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572651 | |||||||
chr14:100572817 | T | A | 1 | a0001c0003t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.43-4878A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572817 | |||||||
chr14:100572915 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43-4976C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572915 | |||||||
chr14:100573172 | A | AGGTGAGT others(31): Show |
2 | a0001c0002t0001g0179 a0001c0002t0001g0263 |
2 | HG02523.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.43-5271_43-5234dup others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | |||||||
chr14:100573172 | A | AGGTGAGT others(69): Show |
1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-5309_43-5234dup others(76): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | |||||||
chr14:100573172 | AGGTGAGT others(31): Show |
A | 1 | a0001c0002t0004g0098 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.43-5271_43-5234del others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | |||||||
chr14:100573187 | G | A | 2 | a0001c0003t0001g0007 a0001c0003t0001g0205 |
4 | HG02451.hp1 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-5248C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573187 | |||||||
chr14:100573207 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-5268C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573207 | |||||||
chr14:100573221 | G | A | 2 | a0001c0003t0001g0013 a0001c0003t0001g0108 |
3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.43-5282C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573221 | |||||||
chr14:100573242 | GGGGGCTG others(31): Show |
G | 22 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(19): Show |
24 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.43-5341_43-5304del others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573242 | |||||||
chr14:100573280 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.43-5341G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573280 | |||||||
chr14:100573297 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.43-5358C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573297 | |||||||
chr14:100573387 | C | T | 54 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.43-5448G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573387 | |||||||
chr14:100573672 | A | G | 2 | a0001c0001t0001g0123 a0001c0002t0001g0120 |
2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.43-5733T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573672 | |||||||
chr14:100573817 | C | T | 3 | a0001c0003t0006g0288 a0001c0003t0006g0289 a0001c0004t0017g0290 |
3 | HG03209.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.43-5878G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573817 | |||||||
chr14:100573933 | C | G | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-5994G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573933 | |||||||
chr14:100574061 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.43-6122G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574061 | |||||||
chr14:100574169 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.43-6230G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574169 | |||||||
chr14:100574370 | T | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-6431A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574370 | |||||||
chr14:100574432 | C | T | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-6493G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574432 | |||||||
chr14:100574443 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(6): Show |
11 | HG02055.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-6504C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574443 | |||||||
chr14:100574518 | G | GT | 17 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0192 others(14): Show |
18 | HG00733.hp1 HG00741.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.43-6580dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | |||||||
chr14:100574518 | GT | G | 73 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(70): Show |
79 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.43-6580delA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | |||||||
chr14:100574518 | GTT | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
96 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.43-6581_43-6580del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | |||||||
chr14:100574518 | GTTT | G | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
19 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-6582_43-6580del others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | |||||||
chr14:100574539 | T | A | 3 | a0001c0001t0001g0036 a0001c0003t0001g0013 a0001c0003t0001g0108 |
4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-6600A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574539 | |||||||
chr14:100574804 | C | T | 3 | a0001c0004t0003g0264 a0001c0004t0003g0265 a0001c0004t0003g0266 |
3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.43-6865G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574804 | |||||||
chr14:100574869 | C | T | 3 | a0001c0001t0001g0036 a0001c0003t0001g0013 a0001c0003t0001g0108 |
4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-6930G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574869 | |||||||
chr14:100574873 | A | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-6934T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574873 | |||||||
chr14:100574887 | C | A | 2 | a0001c0002t0001g0136 a0001c0002t0001g0137 |
2 | NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.43-6948G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574887 | |||||||
chr14:100574889 | C | G | 2 | a0001c0002t0001g0136 a0001c0002t0001g0137 |
2 | NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.43-6950G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574889 | |||||||
chr14:100574995 | C | T | 1 | a0001c0004t0003g0275 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.43-7056G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574995 | |||||||
chr14:100574999 | G | A | 1 | a0001c0005t0002g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43-7060C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574999 | |||||||
chr14:100575172 | A | G | 1 | a0001c0002t0005g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.43-7233T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575172 | |||||||
chr14:100575206 | C | T | 5 | a0001c0002t0006g0286 a0001c0002t0006g0287 a0001c0005t0002g0109 others(2): Show |
5 | HG02055.hp2 HG02723.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-7267G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575206 | |||||||
chr14:100575209 | G | A | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-7270C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575209 | |||||||
chr14:100575211 | A | C | 3 | a0001c0001t0001g0036 a0001c0003t0001g0013 a0001c0003t0001g0108 |
4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-7272T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575211 | |||||||
chr14:100575328 | A | C | 1 | a0001c0005t0010g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43-7389T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575328 | |||||||
chr14:100575407 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.43-7468A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575407 | |||||||
chr14:100575631 | T | C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(18): Show |
23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-7692A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575631 | |||||||
chr14:100575806 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.43-7867C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575806 | |||||||
chr14:100575808 | C | A | 1 | a0001c0002t0001g0190 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.43-7869G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575808 | |||||||
chr14:100575861 | G | T | 2 | a0001c0003t0001g0278 a0001c0005t0010g0107 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-7922C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575861 | |||||||
chr14:100576002 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-8063C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576002 | |||||||
chr14:100576013 | C | T | 1 | a0001c0005t0001g0106 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-8074G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576013 | |||||||
chr14:100576047 | T | A | 3 | a0001c0001t0001g0177 a0001c0002t0001g0172 a0003c0015t0001g0132 |
3 | HG01169.hp2 HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.43-8108A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576047 | |||||||
chr14:100576050 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.43-8111G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576050 | |||||||
chr14:100576132 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43-8193C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576132 | |||||||
chr14:100576148 | C | T | 2 | a0001c0001t0001g0123 a0001c0002t0001g0120 |
2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.43-8209G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576148 | |||||||
chr14:100576378 | A | C | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.43-8439T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576378 | |||||||
chr14:100576386 | G | A | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8447C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576386 | |||||||
chr14:100576462 | G | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0239 a0001c0001t0001g0245 others(5): Show |
8 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-8523C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576462 | |||||||
chr14:100576464 | C | T | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-8525G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576464 | |||||||
chr14:100576637 | C | T | 6 | a0001c0001t0008g0221 a0001c0002t0001g0222 a0001c0002t0001g0223 others(3): Show |
6 | HG00558.hp2 HG01884.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-8698G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576637 | |||||||
chr14:100576726 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-8787G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576726 | |||||||
chr14:100576735 | C | T | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8796G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576735 | |||||||
chr14:100576845 | C | T | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8906G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576845 | |||||||
chr14:100576890 | C | T | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8951G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576890 | |||||||
chr14:100577595 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.42+9654C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577595 | |||||||
chr14:100577766 | G | T | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9483C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577766 | |||||||
chr14:100577849 | T | C | 2 | a0001c0001t0001g0271 a0001c0016t0001g0182 |
2 | HG00544.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.42+9400A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577849 | |||||||
chr14:100577935 | G | A | 2 | a0001c0003t0001g0278 a0001c0005t0010g0107 |
2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.42+9314C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577935 | |||||||
chr14:100577976 | G | A | 1 | a0001c0005t0010g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42+9273C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577976 | |||||||
chr14:100577993 | C | A | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9256G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577993 | |||||||
chr14:100578082 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.42+9167G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578082 | |||||||
chr14:100578091 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.42+9158G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578091 | |||||||
chr14:100578227 | G | A | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9022C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578227 | |||||||
chr14:100578353 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.42+8896T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578353 | |||||||
chr14:100578391 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0173 |
2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.42+8858C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578391 | |||||||
chr14:100578455 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+8794G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578455 | |||||||
chr14:100578631 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.42+8618C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578631 | |||||||
chr14:100578665 | A | G | 11 | a0001c0001t0001g0269 a0001c0002t0001g0101 a0001c0004t0001g0021 others(8): Show |
12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+8584T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578665 | |||||||
chr14:100578794 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+8455A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578794 | |||||||
chr14:100578856 | C | CT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0051 others(17): Show |
23 | HG00639.hp1 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.42+8392dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | |||||||
chr14:100578856 | C | CTT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.42+8391_42+8392dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | |||||||
chr14:100578856 | C | CTTT | 25 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0031 others(22): Show |
28 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.42+8390_42+8392dup others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | |||||||
chr14:100578856 | CT | C | 11 | a0001c0001t0001g0099 a0001c0001t0001g0174 a0001c0001t0001g0176 others(8): Show |
11 | HG01069.hp1 HG01169.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+8392delA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | |||||||
chr14:100578876 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.42+8373A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578876 | |||||||
chr14:100578891 | C | T | 2 | a0001c0001t0001g0016 a0003c0015t0001g0132 |
3 | HG01261.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42+8358G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578891 | |||||||
chr14:100578892 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.42+8357C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578892 | |||||||
chr14:100578918 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.42+8331T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578918 | |||||||
chr14:100578930 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.42+8319G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578930 | |||||||
chr14:100578955 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.42+8294C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578955 | |||||||
chr14:100579034 | T | C | 1 | a0001c0003t0001g0246 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.42+8215A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579034 | |||||||
chr14:100579062 | T | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0014g0248 |
3 | HG01978.hp1 NA18977.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.42+8187A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579062 | |||||||
chr14:100579175 | C | T | 2 | a0001c0004t0002g0006 a0001c0004t0002g0203 |
4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+8074G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579175 | |||||||
chr14:100579471 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.42+7778C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579471 | |||||||
chr14:100579614 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42+7635C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579614 | |||||||
chr14:100579677 | T | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
12 | HG01099.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+7572A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579677 | |||||||
chr14:100579706 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.42+7543C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579706 | |||||||
chr14:100579735 | C | T | 1 | a0001c0002t0001g0131 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.42+7514G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579735 | |||||||
chr14:100579747 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
10 | HG01099.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+7502T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579747 | |||||||
chr14:100579749 | G | C | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+7500C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579749 | |||||||
chr14:100579963 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0214 others(4): Show |
9 | HG00544.hp1 HG00733.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+7286C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579963 | |||||||
chr14:100580028 | G | GGT | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+7219_42+7220dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580028 | |||||||
chr14:100580032 | C | T | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(16): Show |
21 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.42+7217G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580032 | |||||||
chr14:100580079 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.42+7170G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580079 | |||||||
chr14:100580261 | C | A | 1 | a0001c0002t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.42+6988G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580261 | |||||||
chr14:100580312 | C | T | 103 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(100): Show |
115 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.42+6937G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580312 | |||||||
chr14:100580699 | T | C | 1 | a0001c0003t0001g0210 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+6550A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580699 | |||||||
chr14:100580723 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42+6526G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580723 | |||||||
chr14:100580975 | G | A | 3 | a0001c0001t0001g0036 a0001c0003t0001g0013 a0001c0003t0001g0108 |
4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+6274C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580975 | |||||||
chr14:100580979 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.42+6270G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580979 | |||||||
chr14:100580989 | G | A | 2 | a0001c0001t0001g0250 a0001c0002t0001g0251 |
2 | HG02080.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.42+6260C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580989 | |||||||
chr14:100581118 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.42+6131A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581118 | |||||||
chr14:100581163 | T | C | 2 | a0001c0001t0001g0093 a0001c0002t0001g0094 |
2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.42+6086A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581163 | |||||||
chr14:100581198 | C | G | 1 | a0001c0002t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42+6051G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581198 | |||||||
chr14:100581208 | T | A | 3 | a0001c0003t0001g0105 a0001c0003t0001g0278 a0001c0005t0010g0107 |
3 | HG02258.hp1 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.42+6041A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581208 | |||||||
chr14:100581232 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(10): Show |
15 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+6017C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581232 | |||||||
chr14:100581398 | C | T | 4 | a0001c0001t0001g0220 a0001c0005t0002g0218 a0001c0005t0002g0219 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+5851G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581398 | |||||||
chr14:100581467 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+5782G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581467 | |||||||
chr14:100581534 | G | A | 2 | a0001c0005t0002g0022 a0001c0005t0016g0285 |
3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42+5715C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581534 | |||||||
chr14:100581545 | C | T | 1 | a0002c0007t0001g0262 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.42+5704G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581545 | |||||||
chr14:100581557 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+5692C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581557 | |||||||
chr14:100581558 | C | T | 2 | a0001c0005t0002g0022 a0001c0005t0016g0285 |
3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42+5691G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581558 | |||||||
chr14:100581559 | G | A | 1 | a0001c0002t0001g0101 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.42+5690C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581559 | |||||||
chr14:100581669 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
19 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+5580G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581669 | |||||||
chr14:100581954 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5295T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581954 | |||||||
chr14:100581955 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5294G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581955 | |||||||
chr14:100581956 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5293T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581956 | |||||||
chr14:100581957 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5292C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581957 | |||||||
chr14:100581958 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5291G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581958 | |||||||
chr14:100581959 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5290T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581959 | |||||||
chr14:100581960 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5289C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581960 | |||||||
chr14:100581961 | G | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5288C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581961 | |||||||
chr14:100581963 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5286G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581963 | |||||||
chr14:100581965 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5284C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581965 | |||||||
chr14:100581966 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5283T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581966 | |||||||
chr14:100581973 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5276C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581973 | |||||||
chr14:100581974 | G | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5275C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581974 | |||||||
chr14:100581975 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5274T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581975 | |||||||
chr14:100581976 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5273C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581976 | |||||||
chr14:100581978 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5271T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581978 | |||||||
chr14:100581979 | G | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5270C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581979 | |||||||
chr14:100581982 | A | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5267T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581982 | |||||||
chr14:100581987 | G | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5262C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581987 | |||||||
chr14:100581990 | T | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5259A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581990 | |||||||
chr14:100581992 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5257T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581992 | |||||||
chr14:100581994 | G | C | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5255C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581994 | |||||||
chr14:100581996 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5253T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581996 | |||||||
chr14:100581997 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5252C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581997 | |||||||
chr14:100581999 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5250T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581999 | |||||||
chr14:100582000 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5249C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582000 | |||||||
chr14:100582002 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5247T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582002 | |||||||
chr14:100582003 | A | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5246T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582003 | |||||||
chr14:100582004 | A | G | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5245T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582004 | |||||||
chr14:100582005 | C | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5244G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582005 | |||||||
chr14:100582008 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5241C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582008 | |||||||
chr14:100582009 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5240C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582009 | |||||||
chr14:100582017 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5232C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582017 | |||||||
chr14:100582019 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5230C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582019 | |||||||
chr14:100582023 | C | A | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5226G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582023 | |||||||
chr14:100582024 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+5225C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582024 | |||||||
chr14:100582025 | G | T | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5224C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582025 | |||||||
chr14:100582026 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5223C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582026 | |||||||
chr14:100582031 | C | T | 1 | a0001c0003t0001g0210 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+5218G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582031 | |||||||
chr14:100582051 | G | A | 6 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01099.hp2 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+5198C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582051 | |||||||
chr14:100582060 | C | T | 207 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0015 others(204): Show |
223 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.42+5189G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582060 | |||||||
chr14:100582084 | G | A | 5 | a0001c0002t0006g0286 a0001c0002t0006g0287 a0001c0005t0002g0109 others(2): Show |
5 | HG02055.hp2 HG02723.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+5165C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582084 | |||||||
chr14:100582127 | A | AT | 6 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01099.hp2 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+5121dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582127 | |||||||
chr14:100582354 | G | A | 206 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0015 others(203): Show |
221 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.42+4895C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582354 | |||||||
chr14:100582394 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
13 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+4855G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582394 | |||||||
chr14:100582397 | C | T | 1 | a0001c0002t0004g0183 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.42+4852G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582397 | |||||||
chr14:100582423 | G | A | 2 | a0001c0003t0001g0013 a0001c0003t0001g0108 |
3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.42+4826C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582423 | |||||||
chr14:100582439 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
10 | HG01099.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+4810T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582439 | |||||||
chr14:100582563 | T | C | 11 | a0001c0001t0001g0269 a0001c0002t0001g0263 a0001c0004t0001g0021 others(8): Show |
12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+4686A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582563 | |||||||
chr14:100582717 | C | T | 1 | a0001c0003t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+4532G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582717 | |||||||
chr14:100582870 | A | T | 6 | a0001c0001t0001g0113 a0001c0003t0001g0110 a0001c0003t0001g0111 others(3): Show |
6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+4379T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582870 | |||||||
chr14:100583069 | T | C | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+4180A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583069 | |||||||
chr14:100583335 | T | C | 1 | a0001c0003t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+3914A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583335 | |||||||
chr14:100583569 | C | T | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+3680G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583569 | |||||||
chr14:100583632 | CTCTT | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0036 others(6): Show |
11 | HG00621.hp1 HG00639.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+3613_42+3616del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583632 | |||||||
chr14:100583692 | C | CT | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG02055.hp2 HG02071.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+3556dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTT | 12 | a0001c0001t0001g0032 a0001c0001t0001g0269 a0001c0002t0001g0263 others(9): Show |
13 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.42+3551_42+3556dup others(6): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTTT | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0211 others(10): Show |
13 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.42+3550_42+3556dup others(7): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTTT others(1): Show |
26 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0103 others(23): Show |
34 | HG00639.hp1 HG01884.hp2 HG02280.hp1 others(31): Show |
intron_variant | MODIFIER | c.42+3549_42+3556dup others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTTT others(2): Show |
71 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0139 others(68): Show |
73 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.42+3548_42+3556dup others(9): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0199 others(8): Show |
11 | HG01106.hp2 HG01358.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+3547_42+3556dup others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0121 a0001c0002t0001g0120 |
2 | HG00741.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.42+3546_42+3556dup others(11): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583692 | CTTTT | C | 58 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
63 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+3553_42+3556del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | |||||||
chr14:100583887 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.42+3362G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583887 | |||||||
chr14:100584064 | T | C | 1 | a0001c0005t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42+3185A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584064 | |||||||
chr14:100584402 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG03225.hp1 HG03471.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2847G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584402 | |||||||
chr14:100584641 | T | G | 4 | a0001c0003t0006g0288 a0001c0003t0006g0289 a0001c0003t0006g0291 others(1): Show |
4 | HG02717.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+2608A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584641 | |||||||
chr14:100584833 | C | T | 1 | a0001c0009t0001g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2416G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584833 | |||||||
chr14:100584856 | G | C | 1 | a0001c0003t0001g0278 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.42+2393C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584856 | |||||||
chr14:100584856 | G | T | 87 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0123 others(84): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.42+2393C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584856 | |||||||
chr14:100584885 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.42+2364G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584885 | |||||||
chr14:100584935 | C | T | 1 | a0001c0002t0001g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.42+2314G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584935 | |||||||
chr14:100585136 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG00408.hp1 HG01993.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2113C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585136 | |||||||
chr14:100585194 | CCCAT | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0103 a0001c0001t0001g0104 others(24): Show |
31 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.42+2051_42+2054del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | |||||||
chr14:100585194 | CCCATCCA others(1): Show |
C | 169 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(166): Show |
180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.42+2047_42+2054del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | |||||||
chr14:100585194 | CCCATCCA others(5): Show |
C | 1 | a0001c0003t0001g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42+2043_42+2054del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | |||||||
chr14:100585221 | ATCCATCC others(5): Show |
A | 1 | a0001c0002t0001g0261 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.42+2016_42+2027del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585221 | |||||||
chr14:100585225 | ATCCATCC others(1): Show |
A | 11 | a0001c0001t0001g0269 a0001c0002t0001g0263 a0001c0004t0001g0021 others(8): Show |
12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+2016_42+2023del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585225 | |||||||
chr14:100585229 | A | C | 9 | a0001c0001t0001g0271 a0001c0003t0001g0105 a0001c0003t0006g0288 others(6): Show |
10 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+2020T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585229 | |||||||
chr14:100585233 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.42+2016G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585233 | |||||||
chr14:100585259 | TCCATCCA others(6): Show |
T | 1 | a0005c0014t0001g0037 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.42+1977_42+1989del others(13): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585259 | |||||||
chr14:100585330 | ATCCC | A | 11 | a0001c0001t0001g0269 a0001c0002t0001g0263 a0001c0004t0001g0021 others(8): Show |
12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+1915_42+1918del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585330 | |||||||
chr14:100585359 | ATCCC | A | 4 | a0001c0001t0001g0271 a0001c0005t0002g0022 a0001c0005t0016g0285 others(1): Show |
5 | HG02280.hp1 HG02886.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+1886_42+1889del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585359 | |||||||
chr14:100585415 | C | CCCAT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(32): Show |
36 | HG01069.hp1 HG01070.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.42+1830_42+1833dup others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585415 | C | CCCATCCA others(1): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0027 others(16): Show |
20 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.42+1826_42+1833dup others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585415 | C | CCCATCCA others(5): Show |
1 | a0001c0001t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42+1822_42+1833dup others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585415 | CCCAT | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(77): Show |
83 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.42+1830_42+1833del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585415 | CCCATCCA others(1): Show |
C | 12 | a0001c0001t0001g0143 a0001c0001t0001g0178 a0001c0002t0001g0138 others(9): Show |
13 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+1826_42+1833del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585415 | CCCATCCA others(17): Show |
C | 1 | a0001c0005t0010g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42+1810_42+1833del others(24): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | |||||||
chr14:100585469 | C | G | 11 | a0001c0001t0001g0269 a0001c0002t0001g0263 a0001c0004t0001g0021 others(8): Show |
12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+1780G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585469 | |||||||
chr14:100585617 | C | A | 1 | a0001c0001t0001g0274 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.42+1632G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585617 | |||||||
chr14:100585904 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.42+1345G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585904 | |||||||
chr14:100585909 | G | C | 1 | a0001c0004t0003g0275 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+1340C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585909 | |||||||
chr14:100586165 | G | T | 1 | a0001c0002t0001g0035 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.42+1084C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586165 | |||||||
chr14:100586195 | C | T | 1 | a0002c0007t0001g0034 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.42+1054G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586195 | |||||||
chr14:100586251 | G | A | 1 | a0001c0003t0001g0276 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+998C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586251 | |||||||
chr14:100586326 | G | T | 1 | a0001c0002t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.42+923C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586326 | |||||||
chr14:100586403 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.42+846C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586403 | |||||||
chr14:100586785 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.42+464G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586785 | |||||||
chr14:100586811 | C | G | 1 | a0001c0002t0001g0029 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.42+438G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586811 | |||||||
chr14:100586898 | C | A | 1 | a0001c0003t0001g0278 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.42+351G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586898 | |||||||
chr14:100587036 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.42+213G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587036 | |||||||
chr14:100587070 | C | A | 1 | a0001c0002t0005g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.42+179G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587070 | |||||||
chr14:100587108 | C | CG | 5 | a0001c0001t0001g0027 a0001c0001t0007g0024 a0001c0002t0001g0026 others(2): Show |
5 | HG02738.hp2 HG03516.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+140dupC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587108 | |||||||
chr14:100587176 | C | T | 1 | a0004c0011t0009g0023 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.42+73G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587176 |