Item | Value |
---|---|
geneid | 150372 |
ensemblid | ENSG00000235568.7 |
hgncid | 29872 |
symbol | NFAM1 |
name | NFAT activating protein with ITAM motif 1 |
refseq_nuc | NM_145912.8 |
refseq_prot | NP_666017.1 |
ensembl_nuc | ENST00000329021.10 |
ensembl_prot | ENSP00000333680.5 |
mane_status | MANE Select |
chr | chr22 |
start | 42380407 |
end | 42432403 |
strand | - |
ver | v1.2 |
region | chr22:42380407-42432403 |
region5000 | chr22:42375407-42437403 |
regionname0 | NFAM1_chr22_42380407_42432403 |
regionname5000 | NFAM1_chr22_42375407_42437403 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 270 | 358 | 75 | 75 | 144 | 16 | 46 | 104 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0002 | 0/0 | 270 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0003 | 0/0 | 270 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0004 | 0/0 | 270 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0005 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0006 | 0/0 | 270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
a0007 | 0/0 | 270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | MENQP others(265): Show |
chr22 | 42375407 | 42437403 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 810 | 289 | 40 | 53 | 143 | 14 | 37 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0002 | 0/0 | 810 | 30 | 21 | 5 | 1 | 0 | 3 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0003 | 0/0 | 810 | 26 | 7 | 12 | 0 | 2 | 5 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0005 | 0/0 | 810 | 8 | 5 | 3 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0008 | 0/0 | 810 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0012 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0015 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0001c0016 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0002c0004 | 0/0 | 810 | 10 | 10 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0002c0009 | 0/0 | 810 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0003c0006 | 0/0 | 810 | 5 | 5 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0003c0013 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0004c0007 | 0/0 | 810 | 4 | 3 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0004c0017 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0005c0014 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0006c0010 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 | ||
a0007c0011 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | ATGGA others(805): Show |
chr22 | 42375407 | 42437403 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5613 | 73 | 3 | 13 | 35 | 8 | 13 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0002 | 0/0 | 5613 | 61 | 3 | 15 | 32 | 2 | 9 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0003 | 0/0 | 5613 | 41 | 1 | 3 | 31 | 0 | 6 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0004 | 0/0 | 5613 | 4 | 4 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0005 | 0/0 | 5613 | 12 | 7 | 2 | 0 | 0 | 3 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0006 | 0/0 | 5609 | 15 | 0 | 0 | 15 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5604): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0009 | 0/0 | 5613 | 10 | 0 | 0 | 10 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0010 | 0/0 | 5613 | 10 | 0 | 10 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0011 | 1/0 | 5613 | 7 | 1 | 2 | 0 | 2 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0014 | 0/0 | 5614 | 5 | 1 | 2 | 0 | 2 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5609): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0015 | 0/0 | 5613 | 5 | 0 | 0 | 5 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0017 | 0/0 | 5613 | 4 | 4 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0019 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0021 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0022 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0024 | 0/0 | 5613 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0025 | 0/0 | 5613 | 2 | 1 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0026 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0027 | 0/0 | 5613 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0028 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0029 | 0/0 | 5613 | 2 | 1 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0030 | 0/0 | 5613 | 2 | 0 | 1 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0031 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0032 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0033 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0034 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0035 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0036 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0037 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0038 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0039 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0041 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0043 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0044 | 0/0 | 5614 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5609): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0050 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0051 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0054 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0056 | 0/0 | 5614 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5609): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0059 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0060 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0062 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0063 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0064 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0001t0065 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0002t0004 | 0/0 | 5613 | 21 | 19 | 2 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0002t0012 | 0/0 | 5613 | 7 | 1 | 2 | 1 | 0 | 3 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0002t0047 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0002t0049 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0003t0007 | 0/0 | 5613 | 12 | 5 | 5 | 0 | 1 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0003t0008 | 0/0 | 5613 | 12 | 2 | 7 | 0 | 1 | 2 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0003t0042 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0003t0057 | 0/0 | 5614 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5609): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0005 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0013 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0021 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0045 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0048 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0053 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0005t0055 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0008t0004 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0008t0040 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0012t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0015t0003 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0001c0016t0002 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0004t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0004t0013 | 0/0 | 5613 | 5 | 5 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0004t0023 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0004t0046 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0004t0058 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0002c0009t0020 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0003c0006t0016 | 0/0 | 5615 | 5 | 5 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5610): Show |
chr22 | 42375407 | 42437403 |
a0003c0013t0061 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5610): Show |
chr22 | 42375407 | 42437403 |
a0004c0007t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0004c0007t0018 | 0/0 | 5613 | 3 | 2 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0004c0017t0052 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5609): Show |
chr22 | 42375407 | 42437403 |
a0005c0014t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
a0006c0010t0006 | 0/0 | 5609 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5604): Show |
chr22 | 42375407 | 42437403 |
a0007c0011t0003 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | CCCCT others(5608): Show |
chr22 | 42375407 | 42437403 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0005g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0010g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0011g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0014g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0014g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0015g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0015g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0017g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0019g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0019g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0022g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0022g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0024g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0024g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0025g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0025g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0026g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0026g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0027g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0028g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0028g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0029g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0029g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0030g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0030g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0031g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0032g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0033g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0034g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0035g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0036g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0037g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0038g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0039g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0041g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0043g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0044g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0050g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0051g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0054g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0056g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0059g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0060g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0062g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0063g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0064g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0001t0065g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0012g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0047g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0002t0049g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0042g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0003t0057g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0013g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0021g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0045g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0048g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0053g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0005t0055g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0008t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0008t0040g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0015t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0001c0016t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0023g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0023g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0046g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0004t0058g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0009t0020g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0002c0009t0020g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0006t0016g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0006t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0006t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0006t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0006t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0003c0013t0061g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0004c0007t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0004c0007t0018g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0004c0007t0018g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0004c0007t0018g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0004c0017t0052g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0005c0014t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0006c0010t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
a0007c0011t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0007 | g0170 | EUR | GBR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | GBR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00280 | hp2 | a0001 | c0001 | t0014 | g0228 | EUR | FIN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0034 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00438 | hp2 | a0001 | c0001 | t0027 | g0006 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0232 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00639 | hp2 | a0004 | c0007 | t0018 | g0361 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0283 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00673 | hp2 | a0001 | c0001 | t0044 | g0341 | EAS | CHS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00733 | hp2 | a0001 | c0002 | t0047 | g0289 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00735 | hp1 | a0001 | c0003 | t0008 | g0162 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00735 | hp2 | a0001 | c0001 | t0030 | g0204 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0190 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG00741 | hp2 | a0001 | c0005 | t0021 | g0239 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01070 | hp2 | a0001 | c0002 | t0012 | g0014 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01071 | hp2 | a0001 | c0002 | t0012 | g0014 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01074 | hp1 | a0001 | c0003 | t0008 | g0070 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01074 | hp2 | a0001 | c0001 | t0010 | g0189 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01106 | hp1 | a0001 | c0001 | t0011 | g0110 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01109 | hp1 | a0001 | c0005 | t0045 | g0260 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01167 | hp2 | a0001 | c0003 | t0008 | g0179 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01192 | hp2 | a0001 | c0001 | t0029 | g0206 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01243 | hp1 | a0001 | c0015 | t0003 | g0261 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0013 | AMR | PUR | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01255 | hp1 | a0001 | c0016 | t0002 | g0148 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01255 | hp2 | a0001 | c0003 | t0007 | g0161 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0284 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0092 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01258 | hp2 | a0001 | c0001 | t0014 | g0111 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01261 | hp1 | a0001 | c0003 | t0007 | g0166 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0073 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0176 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01433 | hp1 | a0001 | c0001 | t0025 | g0036 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01433 | hp2 | a0001 | c0001 | t0034 | g0106 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01496 | hp1 | a0001 | c0003 | t0008 | g0173 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01496 | hp2 | a0001 | c0002 | t0004 | g0158 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01516 | hp1 | a0001 | c0001 | t0011 | g0041 | EUR | IBS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01517 | hp2 | a0001 | c0001 | t0011 | g0131 | EUR | IBS | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01884 | hp1 | a0001 | c0005 | t0048 | g0259 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01884 | hp2 | a0001 | c0005 | t0055 | g0268 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01891 | hp1 | a0001 | c0003 | t0007 | g0355 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01928 | hp1 | a0001 | c0003 | t0008 | g0171 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01928 | hp2 | a0001 | c0001 | t0010 | g0210 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01934 | hp1 | a0001 | c0005 | t0013 | g0265 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01934 | hp2 | a0001 | c0003 | t0007 | g0177 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01943 | hp2 | a0001 | c0003 | t0007 | g0255 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01975 | hp1 | a0001 | c0001 | t0010 | g0209 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01975 | hp2 | a0001 | c0003 | t0008 | g0165 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0207 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01981 | hp1 | a0001 | c0001 | t0010 | g0208 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01993 | hp1 | a0001 | c0001 | t0063 | g0199 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01993 | hp2 | a0001 | c0003 | t0008 | g0164 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02027 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02040 | hp2 | a0001 | c0001 | t0009 | g0146 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02055 | hp1 | a0001 | c0002 | t0004 | g0353 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02055 | hp2 | a0003 | c0006 | t0016 | g0183 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02056 | hp1 | a0001 | c0001 | t0015 | g0247 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02056 | hp2 | a0001 | c0001 | t0021 | g0089 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02080 | hp1 | a0001 | c0001 | t0036 | g0287 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02135 | hp2 | a0001 | c0001 | t0039 | g0105 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02145 | hp1 | a0001 | c0001 | t0026 | g0033 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0340 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02148 | hp2 | a0001 | c0001 | t0010 | g0211 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CDX | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02155 | hp2 | a0001 | c0001 | t0015 | g0124 | EAS | CDX | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | CDX | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02165 | hp2 | a0001 | c0001 | t0015 | g0084 | EAS | CDX | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02258 | hp1 | a0001 | c0001 | t0043 | g0062 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02280 | hp1 | a0002 | c0004 | t0058 | g0238 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0159 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02293 | hp2 | a0001 | c0001 | t0041 | g0312 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02300 | hp1 | a0001 | c0003 | t0007 | g0178 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02451 | hp1 | a0001 | c0001 | t0022 | g0279 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02451 | hp2 | a0001 | c0001 | t0029 | g0212 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02523 | hp1 | a0001 | c0001 | t0015 | g0055 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02572 | hp1 | a0002 | c0004 | t0013 | g0237 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02572 | hp2 | a0004 | c0007 | t0005 | g0276 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02602 | hp1 | a0001 | c0001 | t0011 | g0091 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02622 | hp2 | a0002 | c0004 | t0003 | g0348 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02630 | hp2 | a0004 | c0007 | t0018 | g0360 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0008 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02647 | hp2 | a0004 | c0017 | t0052 | g0029 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02717 | hp2 | a0001 | c0005 | t0005 | g0258 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02723 | hp2 | a0001 | c0008 | t0040 | g0365 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0282 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02738 | hp2 | a0001 | c0001 | t0065 | g0213 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02809 | hp1 | a0001 | c0001 | t0026 | g0264 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02818 | hp1 | a0005 | c0014 | t0005 | g0027 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02818 | hp2 | a0001 | c0008 | t0004 | g0363 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02886 | hp1 | a0001 | c0001 | t0051 | g0181 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02886 | hp2 | a0001 | c0002 | t0012 | g0350 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0180 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02896 | hp1 | a0004 | c0007 | t0018 | g0358 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0356 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0271 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0357 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02922 | hp1 | a0001 | c0003 | t0007 | g0280 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02922 | hp2 | a0001 | c0001 | t0050 | g0156 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02965 | hp1 | a0001 | c0001 | t0062 | g0352 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0347 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02970 | hp1 | a0001 | c0001 | t0028 | g0344 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02976 | hp1 | a0002 | c0004 | t0013 | g0077 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02976 | hp2 | a0001 | c0001 | t0017 | g0022 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03017 | hp1 | a0001 | c0003 | t0007 | g0168 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03041 | hp1 | a0003 | c0006 | t0016 | g0184 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0157 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03098 | hp2 | a0003 | c0013 | t0061 | g0167 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03130 | hp1 | a0002 | c0009 | t0020 | g0367 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03130 | hp2 | a0002 | c0004 | t0013 | g0236 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03195 | hp1 | a0003 | c0006 | t0016 | g0182 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03195 | hp2 | a0002 | c0004 | t0013 | g0235 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03209 | hp1 | a0001 | c0003 | t0007 | g0263 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0020 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03225 | hp1 | a0001 | c0005 | t0053 | g0351 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03239 | hp2 | a0001 | c0003 | t0008 | g0270 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03453 | hp1 | a0003 | c0006 | t0016 | g0032 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03453 | hp2 | a0001 | c0003 | t0007 | g0174 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03486 | hp1 | a0003 | c0006 | t0016 | g0257 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03486 | hp2 | a0001 | c0002 | t0004 | g0335 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03491 | hp2 | a0001 | c0002 | t0012 | g0336 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03516 | hp1 | a0001 | c0001 | t0064 | g0262 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03516 | hp2 | a0001 | c0002 | t0004 | g0160 | AFR | ESN | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03579 | hp1 | a0002 | c0004 | t0013 | g0234 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03579 | hp2 | a0002 | c0004 | t0046 | g0233 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03654 | hp2 | a0001 | c0012 | t0001 | g0153 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03669 | hp1 | a0001 | c0001 | t0030 | g0203 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0337 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03688 | hp2 | a0001 | c0003 | t0008 | g0163 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0080 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03831 | hp1 | a0001 | c0001 | t0056 | g0286 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03831 | hp2 | a0001 | c0001 | t0033 | g0251 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03834 | hp2 | a0001 | c0003 | t0042 | g0154 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03942 | hp2 | a0001 | c0002 | t0012 | g0198 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04115 | hp1 | a0001 | c0003 | t0057 | g0175 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04115 | hp2 | a0001 | c0001 | t0032 | g0290 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04184 | hp2 | a0001 | c0002 | t0012 | g0197 | SAS | BEB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04199 | hp2 | a0006 | c0010 | t0006 | g0057 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18522 | hp2 | a0001 | c0005 | t0005 | g0079 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0008 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18906 | hp2 | a0001 | c0001 | t0060 | g0018 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18942 | hp1 | a0001 | c0001 | t0009 | g0063 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18945 | hp2 | a0001 | c0001 | t0037 | g0123 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18957 | hp2 | a0001 | c0001 | t0019 | g0081 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18961 | hp1 | a0001 | c0001 | t0019 | g0083 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18962 | hp1 | a0001 | c0001 | t0009 | g0065 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18964 | hp2 | a0001 | c0001 | t0024 | g0090 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18969 | hp1 | a0001 | c0001 | t0019 | g0082 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0050 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18986 | hp1 | a0001 | c0001 | t0015 | g0078 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18990 | hp2 | a0001 | c0001 | t0059 | g0117 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18993 | hp2 | a0001 | c0002 | t0012 | g0227 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0104 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA18999 | hp2 | a0001 | c0001 | t0027 | g0006 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19004 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19030 | hp1 | a0001 | c0003 | t0008 | g0256 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19030 | hp2 | a0001 | c0002 | t0004 | g0269 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19043 | hp2 | a0001 | c0001 | t0054 | g0298 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19054 | hp2 | a0001 | c0001 | t0009 | g0102 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19057 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19060 | hp2 | a0001 | c0001 | t0024 | g0095 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19062 | hp1 | a0001 | c0001 | t0031 | g0023 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19087 | hp1 | a0001 | c0001 | t0035 | g0135 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19090 | hp1 | a0001 | c0001 | t0009 | g0103 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19240 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0252 | AFR | YRI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20129 | hp1 | a0001 | c0001 | t0038 | g0364 | AFR | ASW | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20129 | hp2 | a0002 | c0004 | t0023 | g0076 | AFR | ASW | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20805 | hp1 | a0001 | c0003 | t0008 | g0172 | EUR | TSI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20805 | hp2 | a0001 | c0001 | t0014 | g0129 | EUR | TSI | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | GIH | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20905 | hp2 | a0007 | c0011 | t0003 | g0200 | SAS | GIH | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0275 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02109 | hp1 | a0001 | c0001 | t0028 | g0345 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02486 | hp1 | a0002 | c0009 | t0020 | g0366 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02559 | hp1 | a0001 | c0001 | t0022 | g0278 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG02559 | hp2 | a0001 | c0002 | t0049 | g0349 | AFR | ACB | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG03471 | hp2 | a0001 | c0003 | t0007 | g0346 | AFR | MSL | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG06807 | hp1 | a0002 | c0004 | t0023 | g0354 | AFR | USA | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
HG06807 | hp2 | a0001 | c0001 | t0014 | g0128 | AFR | USA | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20300 | hp1 | a0001 | c0001 | t0025 | g0037 | AFR | USA | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA20300 | hp2 | a0001 | c0003 | t0008 | g0169 | AFR | USA | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
NA21309 | hp2 | a0001 | c0001 | t0017 | g0359 | AFR | LWK | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0244 | REF | REF | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0127 | REF | REF | NFAM1_chr22_42375407_42437403 | NFAM1 | chr22 | 42375407 | 42437403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:42385192 | C | G | 1 | a0003 | 6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.782G>C | p.Gly261Ala | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 828/5613 | 782/813 | 261/270 | chr22 | 42385192 | |||
chr22:42385214 | G | T | 1 | a0005 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.760C>A | p.Pro254Thr | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 806/5613 | 760/813 | 254/270 | chr22 | 42385214 | |||
chr22:42409438 | G | C | 1 | a0002 | 12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
missense_variant | MODERATE | c.561C>G | p.Asn187Lys | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/6 | 607/5613 | 561/813 | 187/270 | chr22 | 42409438 | |||
chr22:42411449 | G | A | 1 | a0004 | 5 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.409C>T | p.His137Tyr | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/6 | 455/5613 | 409/813 | 137/270 | chr22 | 42411449 | |||
chr22:42411491 | C | T | 1 | a0007 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.367G>A | p.Ala123Thr | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/6 | 413/5613 | 367/813 | 123/270 | chr22 | 42411491 | |||
chr22:42411518 | A | C | 1 | a0006 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.340T>G | p.Cys114Gly | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/6 | 386/5613 | 340/813 | 114/270 | chr22 | 42411518 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:42385194 | A | G | 1 | a0001c0015 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.780T>C | p.Asp260Asp | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 826/5613 | 780/813 | 260/270 | chr22 | 42385194 | |||
chr22:42385203 | G | A | 1 | a0001c0016 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.771C>T | p.Phe257Phe | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 817/5613 | 771/813 | 257/270 | chr22 | 42385203 | |||
chr22:42387013 | G | A | 3 | a0001c0002 a0001c0008 a0004c0017 |
33 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(30): Show |
synonymous_variant | LOW | c.729C>T | p.Thr243Thr | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/6 | 775/5613 | 729/813 | 243/270 | chr22 | 42387013 | |||
chr22:42387064 | G | A | 1 | a0001c0003 | 26 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(23): Show |
synonymous_variant | LOW | c.678C>T | p.Arg226Arg | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/6 | 724/5613 | 678/813 | 226/270 | chr22 | 42387064 | |||
chr22:42397867 | A | G | 5 | a0001c0003 a0001c0005 a0001c0008 others(2): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
synonymous_variant | LOW | c.654T>C | p.Ser218Ser | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/6 | 700/5613 | 654/813 | 218/270 | chr22 | 42397867 | |||
chr22:42409525 | C | T | 1 | a0001c0012 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.474G>A | p.Pro158Pro | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/6 | 520/5613 | 474/813 | 158/270 | chr22 | 42409525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:42380527 | C | T | 1 | a0001c0001t0037 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4634G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4634 | chr22 | 42380527 | ||||||
chr22:42380574 | A | G | 1 | a0001c0002t0049 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4587T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4587 | chr22 | 42380574 | ||||||
chr22:42380582 | T | C | 58 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(55): Show |
242 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*4579A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4579 | chr22 | 42380582 | ||||||
chr22:42380603 | A | G | 56 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(53): Show |
237 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*4558T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4558 | chr22 | 42380603 | ||||||
chr22:42380794 | C | CA | 4 | a0001c0001t0014 a0003c0006t0016 a0003c0013t0061 others(1): Show |
12 | HG00280.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4366dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4366 | chr22 | 42380794 | ||||||
chr22:42380804 | AAGAG | A | 2 | a0001c0001t0006 a0006c0010t0006 |
16 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4353_*4356delCTCT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4353 | chr22 | 42380804 | ||||||
chr22:42380962 | G | A | 8 | a0001c0001t0004 a0001c0001t0017 a0001c0002t0004 others(5): Show |
40 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4199C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4199 | chr22 | 42380962 | ||||||
chr22:42380971 | G | T | 1 | a0001c0001t0019 | 3 | NA18957.hp2 NA18961.hp1 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4190C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4190 | chr22 | 42380971 | ||||||
chr22:42381000 | T | A | 1 | a0001c0003t0042 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4161A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 4161 | chr22 | 42381000 | ||||||
chr22:42381200 | G | A | 19 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0022 others(16): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3961C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3961 | chr22 | 42381200 | ||||||
chr22:42381252 | G | T | 1 | a0001c0001t0062 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3909C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3909 | chr22 | 42381252 | ||||||
chr22:42381408 | G | A | 16 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(13): Show |
101 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3753C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3753 | chr22 | 42381408 | ||||||
chr22:42381513 | G | C | 1 | a0001c0001t0063 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3648C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3648 | chr22 | 42381513 | ||||||
chr22:42381615 | A | G | 53 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(50): Show |
222 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*3546T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3546 | chr22 | 42381615 | ||||||
chr22:42381656 | C | T | 53 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(50): Show |
221 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*3505G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3505 | chr22 | 42381656 | ||||||
chr22:42381688 | A | G | 53 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(50): Show |
221 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*3473T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3473 | chr22 | 42381688 | ||||||
chr22:42381710 | G | A | 52 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(49): Show |
220 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*3451C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3451 | chr22 | 42381710 | ||||||
chr22:42381716 | C | T | 1 | a0001c0001t0051 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3445G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3445 | chr22 | 42381716 | ||||||
chr22:42381860 | T | C | 53 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(50): Show |
221 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*3301A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3301 | chr22 | 42381860 | ||||||
chr22:42381929 | A | C | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(52): Show |
224 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*3232T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3232 | chr22 | 42381929 | ||||||
chr22:42381960 | C | T | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(52): Show |
224 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*3201G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3201 | chr22 | 42381960 | ||||||
chr22:42382072 | A | G | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(52): Show |
224 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*3089T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3089 | chr22 | 42382072 | ||||||
chr22:42382110 | C | T | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(52): Show |
224 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*3051G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 3051 | chr22 | 42382110 | ||||||
chr22:42382202 | C | T | 1 | a0001c0001t0041 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2959G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2959 | chr22 | 42382202 | ||||||
chr22:42382204 | T | C | 52 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(49): Show |
215 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2957A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2957 | chr22 | 42382204 | ||||||
chr22:42382319 | A | G | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(52): Show |
224 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*2842T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2842 | chr22 | 42382319 | ||||||
chr22:42382350 | C | T | 1 | a0001c0005t0055 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2811G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2811 | chr22 | 42382350 | ||||||
chr22:42382378 | C | G | 1 | a0001c0005t0048 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2783G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2783 | chr22 | 42382378 | ||||||
chr22:42382607 | A | G | 1 | a0002c0009t0020 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2554T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2554 | chr22 | 42382607 | ||||||
chr22:42382900 | C | T | 1 | a0001c0002t0047 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2261G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2261 | chr22 | 42382900 | ||||||
chr22:42382973 | T | C | 2 | a0001c0001t0025 a0001c0001t0028 |
4 | HG01433.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2188A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2188 | chr22 | 42382973 | ||||||
chr22:42382975 | G | A | 1 | a0001c0001t0043 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2186 | chr22 | 42382975 | ||||||
chr22:42383007 | C | A | 1 | a0001c0001t0036 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2154 | chr22 | 42383007 | ||||||
chr22:42383012 | T | C | 21 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(18): Show |
121 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2149A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2149 | chr22 | 42383012 | ||||||
chr22:42383021 | G | A | 2 | a0001c0001t0026 a0001c0001t0060 |
3 | HG02145.hp1 HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2140C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2140 | chr22 | 42383021 | ||||||
chr22:42383088 | G | A | 1 | a0001c0001t0022 | 2 | HG02451.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2073C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2073 | chr22 | 42383088 | ||||||
chr22:42383148 | C | T | 1 | a0001c0001t0033 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 2013 | chr22 | 42383148 | ||||||
chr22:42383232 | G | A | 1 | a0001c0001t0064 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1929 | chr22 | 42383232 | ||||||
chr22:42383492 | T | C | 1 | a0002c0004t0023 | 2 | HG06807.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1669A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1669 | chr22 | 42383492 | ||||||
chr22:42383628 | C | T | 1 | a0002c0004t0046 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1533G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1533 | chr22 | 42383628 | ||||||
chr22:42383693 | T | C | 64 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(61): Show |
273 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*1468A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1468 | chr22 | 42383693 | ||||||
chr22:42383728 | C | T | 2 | a0003c0006t0016 a0003c0013t0061 |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1433G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1433 | chr22 | 42383728 | ||||||
chr22:42383745 | G | GA | 5 | a0001c0001t0044 a0001c0001t0056 a0001c0003t0057 others(2): Show |
9 | HG00673.hp2 HG02055.hp2 HG03041.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1415_*1416insT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1415 | chr22 | 42383745 | ||||||
chr22:42383746 | T | A | 38 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(35): Show |
181 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*1415A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1415 | chr22 | 42383746 | ||||||
chr22:42383747 | T | C | 6 | a0001c0001t0044 a0001c0001t0056 a0001c0001t0065 others(3): Show |
10 | HG00673.hp2 HG02055.hp2 HG02738.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1414A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1414 | chr22 | 42383747 | ||||||
chr22:42383752 | C | T | 1 | a0001c0001t0009 | 10 | HG00408.hp2 HG02027.hp2 HG02040.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1409G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1409 | chr22 | 42383752 | ||||||
chr22:42383754 | C | T | 1 | a0001c0005t0045 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1407G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1407 | chr22 | 42383754 | ||||||
chr22:42383861 | G | A | 1 | a0004c0007t0018 | 3 | HG00639.hp2 HG02630.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1300 | chr22 | 42383861 | ||||||
chr22:42383873 | G | A | 34 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0017 others(31): Show |
113 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1288C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1288 | chr22 | 42383873 | ||||||
chr22:42383874 | G | A | 34 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0017 others(31): Show |
113 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1287C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1287 | chr22 | 42383874 | ||||||
chr22:42383894 | G | A | 9 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0029 others(6): Show |
53 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1267C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 1267 | chr22 | 42383894 | ||||||
chr22:42384183 | G | A | 2 | a0001c0001t0026 a0001c0001t0060 |
3 | HG02145.hp1 HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*978C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 978 | chr22 | 42384183 | ||||||
chr22:42384325 | G | C | 77 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(74): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*836C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 836 | chr22 | 42384325 | ||||||
chr22:42384333 | G | A | 1 | a0001c0001t0059 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*828C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 828 | chr22 | 42384333 | ||||||
chr22:42384333 | G | C | 1 | a0002c0004t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 828 | chr22 | 42384333 | ||||||
chr22:42384459 | G | C | 7 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0025 others(4): Show |
25 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*702C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 702 | chr22 | 42384459 | ||||||
chr22:42384506 | C | T | 1 | a0001c0001t0001 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 655 | chr22 | 42384506 | ||||||
chr22:42384594 | C | A | 1 | a0001c0001t0027 | 2 | HG00438.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*567G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 567 | chr22 | 42384594 | ||||||
chr22:42384644 | G | T | 1 | a0001c0001t0032 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 517 | chr22 | 42384644 | ||||||
chr22:42384678 | A | G | 1 | a0002c0009t0020 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*483T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 483 | chr22 | 42384678 | ||||||
chr22:42384711 | T | C | 1 | a0001c0001t0028 | 2 | HG02109.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*450A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 450 | chr22 | 42384711 | ||||||
chr22:42384979 | T | C | 11 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0019 others(8): Show |
64 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*182A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 182 | chr22 | 42384979 | ||||||
chr22:42385002 | G | A | 2 | a0003c0006t0016 a0003c0013t0061 |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*159C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 159 | chr22 | 42385002 | ||||||
chr22:42385065 | G | A | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0019 others(9): Show |
65 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 96 | chr22 | 42385065 | ||||||
chr22:42385099 | G | T | 1 | a0001c0001t0031 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 6/6 | 62 | chr22 | 42385099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:42385273 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.754-53A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385273 | |||||||
chr22:42385398 | T | G | 1 | a0002c0004t0013g0237 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.754-178A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385398 | |||||||
chr22:42385690 | C | T | 5 | a0001c0005t0005g0079 a0001c0005t0005g0258 a0001c0005t0045g0260 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-470G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385690 | |||||||
chr22:42385744 | C | G | 1 | a0001c0001t0056g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.754-524G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385744 | |||||||
chr22:42385820 | A | G | 1 | a0001c0001t0025g0036 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.754-600T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385820 | |||||||
chr22:42385823 | G | A | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-603C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385823 | |||||||
chr22:42385910 | T | C | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.754-690A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42385910 | |||||||
chr22:42386038 | A | G | 1 | a0004c0007t0018g0360 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.754-818T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386038 | |||||||
chr22:42386096 | C | T | 61 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(58): Show |
64 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.754-876G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386096 | |||||||
chr22:42386145 | T | C | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+844A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386145 | |||||||
chr22:42386247 | G | C | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+742C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386247 | |||||||
chr22:42386303 | A | G | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+686T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386303 | |||||||
chr22:42386330 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.753+659G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386330 | |||||||
chr22:42386331 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0132 |
2 | HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.753+658C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386331 | |||||||
chr22:42386364 | A | G | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.753+625T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386364 | |||||||
chr22:42386392 | A | AAC | 87 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0149 others(84): Show |
92 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.753+595_753+596dup others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACAC | 44 | a0001c0001t0002g0015 a0001c0001t0002g0061 a0001c0001t0002g0145 others(41): Show |
44 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.753+596_753+597ins others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACAC | 13 | a0001c0001t0002g0293 a0001c0001t0002g0302 a0001c0001t0002g0307 others(10): Show |
13 | HG01099.hp1 HG02896.hp2 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.753+596_753+597ins others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(1): Show |
8 | a0001c0001t0002g0297 a0001c0001t0002g0316 a0001c0001t0004g0031 others(5): Show |
8 | HG02717.hp1 NA18947.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+596_753+597ins others(8): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(3): Show |
2 | a0001c0001t0025g0036 a0001c0001t0025g0037 |
2 | HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753+596_753+597ins others(10): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(5): Show |
1 | a0001c0001t0006g0050 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.753+596_753+597ins others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(7): Show |
9 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0052 others(6): Show |
9 | HG02083.hp1 HG02129.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+596_753+597ins others(14): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(9): Show |
7 | a0001c0001t0006g0056 a0001c0001t0026g0264 a0001c0001t0028g0344 others(4): Show |
7 | HG02074.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+596_753+597ins others(16): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386392 | A | AACACACA others(11): Show |
2 | a0001c0001t0006g0048 a0003c0006t0016g0183 |
2 | HG02055.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.753+596_753+597ins others(18): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386392 | |||||||
chr22:42386394 | CAA | C | 34 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0043g0062 others(31): Show |
35 | HG00735.hp1 HG01167.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.753+593_753+594del others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386394 | |||||||
chr22:42386396 | A | AAC | 30 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0067 others(27): Show |
33 | HG00609.hp2 HG00733.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.753+591_753+592dup others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386396 | |||||||
chr22:42386396 | A | AACAC | 11 | a0001c0001t0001g0039 a0001c0001t0001g0093 a0001c0002t0004g0001 others(8): Show |
15 | HG01496.hp2 HG02083.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.753+589_753+592dup others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386396 | |||||||
chr22:42386396 | A | C | 192 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0015 others(189): Show |
197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.753+593T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386396 | |||||||
chr22:42386429 | A | C | 1 | a0001c0001t0006g0045 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.753+560T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386429 | |||||||
chr22:42386433 | A | C | 1 | a0001c0001t0006g0045 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.753+556T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386433 | |||||||
chr22:42386437 | CA | C | 189 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(186): Show |
195 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.753+551delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386437 | |||||||
chr22:42386437 | CAA | C | 14 | a0001c0001t0005g0025 a0001c0001t0005g0281 a0001c0001t0005g0282 others(11): Show |
14 | HG00642.hp2 HG01256.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.753+550_753+551del others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386437 | |||||||
chr22:42386444 | AAAG | A | 22 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(19): Show |
22 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.753+542_753+544del others(3): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386444 | |||||||
chr22:42386447 | G | A | 1 | a0001c0001t0006g0045 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.753+542C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386447 | |||||||
chr22:42386453 | A | G | 23 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(20): Show |
23 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.753+536T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386453 | |||||||
chr22:42386573 | G | A | 16 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(13): Show |
16 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.753+416C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386573 | |||||||
chr22:42386588 | A | C | 1 | a0002c0004t0023g0354 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.753+401T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386588 | |||||||
chr22:42386612 | T | C | 2 | a0001c0001t0025g0036 a0001c0001t0025g0037 |
2 | HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.753+377A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386612 | |||||||
chr22:42386641 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.753+348C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386641 | |||||||
chr22:42386643 | C | T | 16 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(13): Show |
16 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.753+346G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386643 | |||||||
chr22:42386838 | T | C | 3 | a0001c0001t0002g0288 a0001c0001t0002g0332 a0001c0001t0002g0343 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.753+151A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386838 | |||||||
chr22:42386862 | C | T | 1 | a0004c0007t0005g0276 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.753+127G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386862 | |||||||
chr22:42386921 | C | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0035 |
3 | HG02109.hp2 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.753+68G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386921 | |||||||
chr22:42386921 | C | T | 8 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(5): Show |
8 | HG02615.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.753+68G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 5/5 | chr22 | 42386921 | |||||||
chr22:42387090 | G | A | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-12C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387090 | |||||||
chr22:42387124 | G | T | 25 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(22): Show |
25 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.664-46C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387124 | |||||||
chr22:42387171 | C | T | 1 | a0001c0001t0037g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.664-93G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387171 | |||||||
chr22:42387216 | C | G | 1 | a0001c0003t0007g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.664-138G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387216 | |||||||
chr22:42387221 | A | AC | 10 | a0001c0001t0001g0108 a0001c0001t0001g0151 a0001c0001t0001g0295 others(7): Show |
10 | HG00642.hp1 HG00673.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.664-144dupG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387221 | |||||||
chr22:42387226 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0334 |
3 | HG04204.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.664-148G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387226 | |||||||
chr22:42387259 | G | A | 1 | a0002c0004t0013g0237 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.664-181C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387259 | |||||||
chr22:42387294 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.664-216G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387294 | |||||||
chr22:42387460 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664-382G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387460 | |||||||
chr22:42387500 | C | T | 60 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(57): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.664-422G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387500 | |||||||
chr22:42387590 | G | C | 60 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(57): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.664-512C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387590 | |||||||
chr22:42387693 | C | A | 1 | a0001c0001t0002g0324 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.664-615G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387693 | |||||||
chr22:42387742 | C | T | 1 | a0001c0001t0062g0352 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664-664G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387742 | |||||||
chr22:42387824 | C | T | 37 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(34): Show |
37 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.664-746G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387824 | |||||||
chr22:42387911 | C | T | 135 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(132): Show |
141 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.664-833G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387911 | |||||||
chr22:42387934 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.664-856C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42387934 | |||||||
chr22:42388087 | C | T | 7 | a0001c0001t0002g0122 a0001c0001t0005g0059 a0001c0001t0005g0060 others(4): Show |
7 | HG00639.hp2 HG02080.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1009G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388087 | |||||||
chr22:42388195 | C | T | 18 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0005g0281 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.664-1117G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388195 | |||||||
chr22:42388211 | C | CT | 226 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(223): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.664-1134dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388211 | |||||||
chr22:42388213 | G | C | 226 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(223): Show |
232 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.664-1135C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388213 | |||||||
chr22:42388468 | G | A | 1 | a0001c0001t0054g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.664-1390C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388468 | |||||||
chr22:42388586 | G | A | 1 | a0001c0001t0002g0324 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.664-1508C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388586 | |||||||
chr22:42388938 | C | T | 1 | a0001c0003t0008g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.664-1860G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42388938 | |||||||
chr22:42389041 | AC | A | 6 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0054g0298 others(3): Show |
6 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-1964delG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389041 | |||||||
chr22:42389054 | C | G | 68 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(65): Show |
68 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.664-1976G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389054 | |||||||
chr22:42389115 | G | A | 20 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(17): Show |
20 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-2037C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389115 | |||||||
chr22:42389271 | CA | C | 6 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-2194delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389271 | |||||||
chr22:42389293 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG00733.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.664-2215C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389293 | |||||||
chr22:42389311 | C | T | 1 | a0001c0001t0062g0352 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664-2233G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389311 | |||||||
chr22:42389336 | G | A | 1 | a0001c0003t0007g0280 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.664-2258C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389336 | |||||||
chr22:42389373 | T | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(30): Show |
33 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(30): Show |
intron_variant | MODIFIER | c.664-2295A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389373 | |||||||
chr22:42389421 | C | T | 1 | a0001c0003t0007g0166 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.664-2343G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389421 | |||||||
chr22:42389432 | T | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(30): Show |
33 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(30): Show |
intron_variant | MODIFIER | c.664-2354A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389432 | |||||||
chr22:42389659 | G | T | 6 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0054g0298 others(3): Show |
6 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-2581C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389659 | |||||||
chr22:42389716 | CTGTT | C | 6 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0054g0298 others(3): Show |
6 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-2642_664-2639d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389716 | |||||||
chr22:42389843 | G | C | 1 | a0001c0001t0002g0324 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.664-2765C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389843 | |||||||
chr22:42389907 | G | T | 1 | a0001c0001t0062g0352 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.664-2829C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42389907 | |||||||
chr22:42390077 | C | T | 1 | a0001c0003t0007g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.664-2999G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390077 | |||||||
chr22:42390388 | G | A | 31 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(28): Show |
31 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.664-3310C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390388 | |||||||
chr22:42390445 | G | A | 24 | a0001c0001t0001g0141 a0001c0001t0006g0042 a0001c0001t0006g0043 others(21): Show |
24 | HG01433.hp1 HG02040.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.664-3367C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390445 | |||||||
chr22:42390511 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG00597.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.664-3433C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390511 | |||||||
chr22:42390534 | G | A | 3 | a0001c0001t0019g0081 a0001c0001t0019g0082 a0001c0001t0019g0083 |
3 | NA18957.hp2 NA18961.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.664-3456C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390534 | |||||||
chr22:42390538 | T | C | 68 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(65): Show |
68 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.664-3460A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390538 | |||||||
chr22:42390685 | C | T | 2 | a0001c0001t0002g0314 a0001c0001t0002g0326 |
2 | HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.664-3607G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390685 | |||||||
chr22:42390795 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.664-3717G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390795 | |||||||
chr22:42390814 | C | T | 92 | a0001c0001t0003g0007 a0001c0001t0003g0009 a0001c0001t0003g0010 others(89): Show |
95 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.664-3736G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390814 | |||||||
chr22:42390816 | C | CAA | 21 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.664-3740_664-3739d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390816 | |||||||
chr22:42390816 | C | CAAAA | 41 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(38): Show |
41 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.664-3742_664-3739d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390816 | |||||||
chr22:42390816 | CA | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.664-3739delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390816 | |||||||
chr22:42390824 | A | T | 4 | a0001c0002t0004g0013 a0001c0002t0004g0024 a0001c0002t0004g0335 others(1): Show |
5 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-3746T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390824 | |||||||
chr22:42390842 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.664-3764T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390842 | |||||||
chr22:42390879 | C | T | 10 | a0001c0005t0013g0265 a0002c0004t0013g0077 a0002c0004t0013g0234 others(7): Show |
10 | HG01934.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-3801G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42390879 | |||||||
chr22:42391037 | C | T | 45 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(42): Show |
45 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.664-3959G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391037 | |||||||
chr22:42391095 | T | A | 45 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(42): Show |
45 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.664-4017A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391095 | |||||||
chr22:42391177 | T | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0035 |
3 | HG02109.hp2 HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.664-4099A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391177 | |||||||
chr22:42391272 | G | A | 39 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(36): Show |
39 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.664-4194C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391272 | |||||||
chr22:42391276 | T | C | 18 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.664-4198A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391276 | |||||||
chr22:42391299 | G | A | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.664-4221C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391299 | |||||||
chr22:42391465 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0250 |
2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.664-4387C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391465 | |||||||
chr22:42391536 | G | C | 1 | a0001c0001t0003g0072 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.664-4458C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391536 | |||||||
chr22:42391945 | C | CA | 100 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0134 others(97): Show |
107 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.664-4868dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391945 | |||||||
chr22:42391945 | C | CAA | 22 | a0001c0001t0003g0071 a0001c0001t0003g0097 a0001c0001t0003g0113 others(19): Show |
22 | HG00408.hp1 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.664-4869_664-4868d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391945 | |||||||
chr22:42391945 | CA | C | 17 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0136 others(14): Show |
17 | HG00639.hp2 HG01071.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-4868delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391945 | |||||||
chr22:42391945 | CAA | C | 35 | a0001c0001t0002g0343 a0001c0003t0007g0161 a0001c0003t0007g0166 others(32): Show |
35 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.664-4869_664-4868d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391945 | |||||||
chr22:42391945 | CAAA | C | 15 | a0001c0003t0008g0165 a0001c0005t0005g0079 a0001c0005t0005g0258 others(12): Show |
15 | HG01109.hp1 HG01884.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.664-4870_664-4868d others(5): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391945 | |||||||
chr22:42391971 | C | T | 1 | a0001c0001t0014g0228 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.664-4893G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42391971 | |||||||
chr22:42392188 | AG | A | 58 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(55): Show |
61 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.664-5111delC | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392188 | |||||||
chr22:42392256 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.664-5178T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392256 | |||||||
chr22:42392310 | G | T | 18 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.664-5232C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392310 | |||||||
chr22:42392474 | G | A | 51 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(48): Show |
51 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.663+5384C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392474 | |||||||
chr22:42392812 | T | C | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.663+5046A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392812 | |||||||
chr22:42392913 | T | C | 53 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(50): Show |
53 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.663+4945A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392913 | |||||||
chr22:42392956 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0151 others(1): Show |
4 | HG02080.hp1 NA18977.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+4902A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42392956 | |||||||
chr22:42393198 | C | T | 4 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0029g0206 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+4660G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393198 | |||||||
chr22:42393286 | T | C | 1 | a0001c0001t0002g0342 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.663+4572A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393286 | |||||||
chr22:42393381 | G | GA | 18 | a0001c0001t0005g0025 a0001c0001t0005g0059 a0001c0001t0005g0060 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.663+4476dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393381 | |||||||
chr22:42393432 | G | A | 12 | a0001c0001t0005g0025 a0001c0001t0005g0281 a0001c0001t0005g0282 others(9): Show |
12 | HG00642.hp2 HG01256.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.663+4426C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393432 | |||||||
chr22:42393440 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0043g0062 others(18): Show |
24 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.663+4418C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393440 | |||||||
chr22:42393464 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.663+4394T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393464 | |||||||
chr22:42393514 | T | G | 4 | a0001c0001t0002g0293 a0001c0001t0002g0302 a0001c0001t0002g0315 others(1): Show |
4 | NA18971.hp1 NA18983.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+4344A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393514 | |||||||
chr22:42393573 | T | A | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.663+4285A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393573 | |||||||
chr22:42393575 | A | AT | 127 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(124): Show |
130 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.663+4282dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393575 | |||||||
chr22:42393575 | A | T | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.663+4283T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393575 | |||||||
chr22:42393590 | G | T | 12 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0062g0352 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.663+4268C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393590 | |||||||
chr22:42393809 | C | A | 5 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(2): Show |
5 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+4049G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393809 | |||||||
chr22:42393943 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0067 others(3): Show |
7 | NA18612.hp2 NA18950.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+3915G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393943 | |||||||
chr22:42393944 | G | A | 1 | a0001c0012t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.663+3914C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393944 | |||||||
chr22:42393973 | T | C | 1 | a0001c0002t0012g0014 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.663+3885A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42393973 | |||||||
chr22:42394128 | C | T | 4 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0005g0356 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+3730G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394128 | |||||||
chr22:42394266 | C | A | 1 | a0001c0001t0002g0292 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.663+3592G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394266 | |||||||
chr22:42394377 | T | A | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.663+3481A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394377 | |||||||
chr22:42394477 | C | T | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.663+3381G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394477 | |||||||
chr22:42394612 | C | T | 48 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(45): Show |
48 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.663+3246G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394612 | |||||||
chr22:42394697 | C | A | 48 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(45): Show |
48 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.663+3161G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394697 | |||||||
chr22:42394706 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.663+3152T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394706 | |||||||
chr22:42394790 | C | T | 2 | a0001c0001t0005g0017 a0001c0001t0005g0021 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.663+3068G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394790 | |||||||
chr22:42394867 | C | T | 104 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(101): Show |
109 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.663+2991G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394867 | |||||||
chr22:42394981 | C | T | 3 | a0001c0001t0026g0033 a0001c0001t0026g0264 a0001c0001t0060g0018 |
3 | HG02145.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.663+2877G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42394981 | |||||||
chr22:42395048 | C | T | 11 | a0001c0001t0010g0176 a0001c0001t0010g0189 a0001c0001t0010g0190 others(8): Show |
11 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.663+2810G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395048 | |||||||
chr22:42395066 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0226 a0001c0001t0021g0089 others(2): Show |
5 | HG02056.hp2 HG04184.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+2792G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395066 | |||||||
chr22:42395123 | A | G | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+2735T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395123 | |||||||
chr22:42395173 | C | CA | 29 | a0001c0001t0001g0112 a0001c0001t0001g0132 a0001c0001t0001g0151 others(26): Show |
29 | HG01099.hp2 HG01433.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.663+2684dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395173 | |||||||
chr22:42395173 | C | CAA | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0003c0006t0016g0032 others(4): Show |
7 | HG02055.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+2683_663+2684d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395173 | |||||||
chr22:42395436 | G | A | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+2422C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395436 | |||||||
chr22:42395483 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.663+2375T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395483 | |||||||
chr22:42395657 | C | T | 1 | a0001c0003t0007g0161 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.663+2201G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395657 | |||||||
chr22:42395658 | G | A | 61 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(58): Show |
64 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.663+2200C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395658 | |||||||
chr22:42395698 | T | C | 1 | a0001c0002t0012g0227 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.663+2160A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395698 | |||||||
chr22:42395743 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0306 |
4 | HG02602.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+2115G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395743 | |||||||
chr22:42395775 | T | A | 1 | a0001c0003t0007g0280 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.663+2083A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395775 | |||||||
chr22:42395813 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.663+2045C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395813 | |||||||
chr22:42395837 | C | T | 5 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(2): Show |
5 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+2021G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395837 | |||||||
chr22:42395838 | G | A | 1 | a0001c0003t0042g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.663+2020C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395838 | |||||||
chr22:42395861 | C | T | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663+1997G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395861 | |||||||
chr22:42395881 | C | CA | 52 | a0001c0001t0001g0002 a0001c0001t0001g0306 a0001c0001t0002g0015 others(49): Show |
54 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.663+1976dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395881 | |||||||
chr22:42395881 | C | CAA | 60 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(57): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.663+1975_663+1976d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395881 | |||||||
chr22:42395881 | CAAAA | C | 18 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(15): Show |
20 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.663+1973_663+1976d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395881 | |||||||
chr22:42395951 | T | TA | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+1906dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42395951 | |||||||
chr22:42396009 | C | T | 60 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(57): Show |
63 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.663+1849G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396009 | |||||||
chr22:42396154 | G | C | 184 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0003g0007 others(181): Show |
189 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.663+1704C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396154 | |||||||
chr22:42396204 | C | T | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+1654G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396204 | |||||||
chr22:42396320 | A | G | 10 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.663+1538T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396320 | |||||||
chr22:42396368 | C | T | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+1490G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396368 | |||||||
chr22:42396384 | T | C | 15 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(12): Show |
15 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.663+1474A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396384 | |||||||
chr22:42396483 | T | TTA | 6 | a0001c0001t0028g0344 a0003c0006t0016g0032 a0003c0006t0016g0182 others(3): Show |
6 | HG02055.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+1373_663+1374d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396483 | |||||||
chr22:42396483 | TTA | T | 183 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0002g0003 others(180): Show |
195 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.663+1373_663+1374d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396483 | |||||||
chr22:42396483 | TTATA | T | 46 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(43): Show |
46 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.663+1371_663+1374d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396483 | |||||||
chr22:42396669 | G | A | 3 | a0001c0003t0007g0177 a0001c0003t0007g0178 a0001c0003t0007g0255 |
3 | HG01934.hp2 HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.663+1189C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396669 | |||||||
chr22:42396671 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0107 |
3 | NA18962.hp2 NA19009.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.663+1187C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396671 | |||||||
chr22:42396845 | C | A | 2 | a0001c0001t0022g0278 a0001c0001t0022g0279 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.663+1013G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396845 | |||||||
chr22:42396890 | G | A | 5 | a0001c0005t0005g0079 a0001c0005t0005g0258 a0001c0005t0045g0260 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+968C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396890 | |||||||
chr22:42396894 | G | A | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+964C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396894 | |||||||
chr22:42396921 | A | AGGGGGCG others(8): Show |
48 | a0001c0001t0002g0015 a0001c0001t0002g0231 a0001c0001t0002g0288 others(45): Show |
48 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.663+922_663+936dup others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396921 | |||||||
chr22:42396921 | AGGGGGCG others(8): Show |
A | 4 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0022 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+922_663+936del others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396921 | |||||||
chr22:42396925 | G | GGCGTGCA others(8): Show |
46 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(43): Show |
46 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.663+932_663+933ins others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396925 | |||||||
chr22:42396927 | C | CGTGCACC others(8): Show |
1 | a0001c0003t0008g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.663+930_663+931ins others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396927 | |||||||
chr22:42396955 | A | G | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+903T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42396955 | |||||||
chr22:42397052 | G | A | 3 | a0002c0004t0013g0235 a0002c0004t0023g0076 a0002c0004t0023g0354 |
3 | HG03195.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.663+806C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397052 | |||||||
chr22:42397116 | C | T | 53 | a0001c0001t0001g0155 a0001c0001t0004g0026 a0001c0001t0004g0028 others(50): Show |
55 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.663+742G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397116 | |||||||
chr22:42397134 | G | A | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.663+724C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397134 | |||||||
chr22:42397207 | C | G | 5 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(2): Show |
5 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.663+651G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397207 | |||||||
chr22:42397401 | G | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.663+457C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397401 | |||||||
chr22:42397451 | G | A | 4 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0022 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+407C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397451 | |||||||
chr22:42397557 | G | A | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+301C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397557 | |||||||
chr22:42397666 | C | T | 2 | a0001c0001t0005g0017 a0001c0001t0005g0021 |
2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.663+192G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397666 | |||||||
chr22:42397728 | T | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.663+130A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397728 | |||||||
chr22:42397839 | C | T | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.663+19G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397839 | |||||||
chr22:42397849 | G | C | 1 | a0003c0006t0016g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.663+9C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 4/5 | chr22 | 42397849 | |||||||
chr22:42397981 | C | T | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.565-25G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42397981 | |||||||
chr22:42398171 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.565-215C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398171 | |||||||
chr22:42398198 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.565-242C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398198 | |||||||
chr22:42398224 | C | T | 114 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0003g0007 others(111): Show |
119 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.565-268G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398224 | |||||||
chr22:42398231 | G | A | 42 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(39): Show |
42 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-275C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398231 | |||||||
chr22:42398264 | G | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.565-308C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398264 | |||||||
chr22:42398320 | T | C | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.565-364A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398320 | |||||||
chr22:42398363 | C | CCT | 161 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0003g0007 others(158): Show |
166 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.565-409_565-408dup others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398363 | |||||||
chr22:42398382 | T | TTTA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0085 others(59): Show |
66 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.565-429_565-427dup others(3): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | T | TTTATTA | 60 | a0001c0001t0001g0093 a0001c0001t0001g0118 a0001c0001t0001g0133 others(57): Show |
66 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.565-432_565-427dup others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | T | TTTATTAT others(2): Show |
7 | a0001c0001t0001g0116 a0001c0001t0002g0314 a0001c0001t0002g0316 others(4): Show |
7 | HG02083.hp1 HG02135.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-435_565-427dup others(9): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | T | TTTATTAT others(5): Show |
3 | a0001c0001t0002g0011 a0001c0001t0002g0305 a0001c0001t0002g0309 |
4 | HG01070.hp1 HG01192.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-438_565-427dup others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | T | TTTATTAT others(8): Show |
2 | a0001c0001t0002g0231 a0001c0001t0002g0318 |
2 | NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.565-441_565-427dup others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | T | TTTATTTA others(3): Show |
1 | a0001c0001t0002g0296 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.565-427_565-426ins others(10): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTA | T | 38 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0136 others(35): Show |
38 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.565-429_565-427del others(3): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTATTA | T | 11 | a0001c0001t0001g0005 a0001c0001t0002g0329 a0001c0001t0002g0330 others(8): Show |
12 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-432_565-427del others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTATTAT others(2): Show |
T | 3 | a0001c0001t0001g0119 a0001c0001t0054g0298 a0001c0003t0008g0256 |
3 | NA19030.hp1 NA19043.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.565-435_565-427del others(9): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTATTAT others(5): Show |
T | 5 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0029g0206 others(2): Show |
5 | HG01081.hp1 HG01192.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.565-438_565-427del others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTATTAT others(8): Show |
T | 57 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(54): Show |
60 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.565-441_565-427del others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398382 | TTTATTAT others(20): Show |
T | 2 | a0001c0001t0005g0356 a0001c0001t0005g0357 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.565-453_565-427del others(27): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398382 | |||||||
chr22:42398385 | A | T | 1 | a0001c0005t0005g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.565-429T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398385 | |||||||
chr22:42398388 | A | T | 4 | a0001c0005t0005g0079 a0001c0005t0045g0260 a0001c0005t0048g0259 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-432T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398388 | |||||||
chr22:42398397 | A | T | 4 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0029g0206 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-441T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398397 | |||||||
chr22:42398400 | A | T | 56 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(53): Show |
59 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.565-444T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398400 | |||||||
chr22:42398515 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.565-559G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398515 | |||||||
chr22:42398516 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0069 others(5): Show |
10 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.565-560C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398516 | |||||||
chr22:42398553 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.565-597G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398553 | |||||||
chr22:42398608 | G | T | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.565-652C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398608 | |||||||
chr22:42398634 | G | A | 47 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(44): Show |
47 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.565-678C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398634 | |||||||
chr22:42398667 | C | T | 4 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0022 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-711G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398667 | |||||||
chr22:42398668 | G | A | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-712C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398668 | |||||||
chr22:42398683 | G | A | 59 | a0001c0001t0001g0067 a0001c0001t0001g0216 a0001c0001t0003g0007 others(56): Show |
62 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.565-727C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398683 | |||||||
chr22:42398886 | C | T | 18 | a0001c0001t0001g0155 a0001c0001t0004g0026 a0001c0001t0004g0028 others(15): Show |
18 | HG01934.hp1 HG02145.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.565-930G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42398886 | |||||||
chr22:42399141 | G | T | 9 | a0001c0001t0002g0035 a0001c0001t0004g0031 a0001c0001t0005g0025 others(6): Show |
9 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.565-1185C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399141 | |||||||
chr22:42399195 | C | T | 78 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(75): Show |
81 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.565-1239G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399195 | |||||||
chr22:42399207 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.565-1251C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399207 | |||||||
chr22:42399231 | G | T | 23 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(20): Show |
25 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.565-1275C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399231 | |||||||
chr22:42399239 | G | A | 117 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(114): Show |
122 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.565-1283C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399239 | |||||||
chr22:42399241 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.565-1285C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399241 | |||||||
chr22:42399446 | C | CA | 74 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(71): Show |
78 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.565-1491dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399446 | |||||||
chr22:42399458 | AAAAAAG | A | 66 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(63): Show |
69 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.565-1508_565-1503d others(8): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399458 | |||||||
chr22:42399459 | AAAAAG | A | 22 | a0001c0001t0001g0155 a0001c0001t0004g0028 a0001c0001t0004g0030 others(19): Show |
22 | HG02074.hp1 HG02257.hp2 HG02615.hp2 others(19): Show |
intron_variant | MODIFIER | c.565-1508_565-1504d others(7): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399459 | |||||||
chr22:42399661 | G | A | 2 | a0001c0001t0026g0264 a0001c0005t0013g0265 |
2 | HG01934.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.565-1705C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399661 | |||||||
chr22:42399706 | G | A | 1 | a0001c0001t0002g0292 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.565-1750C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399706 | |||||||
chr22:42399727 | G | A | 4 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0029g0206 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-1771C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399727 | |||||||
chr22:42399834 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0026g0033 a0001c0001t0026g0264 others(11): Show |
19 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-1878G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399834 | |||||||
chr22:42399875 | T | C | 4 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-1919A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399875 | |||||||
chr22:42399893 | C | A | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.565-1937G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399893 | |||||||
chr22:42399934 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.565-1978C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42399934 | |||||||
chr22:42400025 | C | T | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-2069G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400025 | |||||||
chr22:42400076 | C | T | 3 | a0001c0001t0003g0071 a0001c0001t0003g0196 a0007c0011t0003g0200 |
3 | HG03688.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.565-2120G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400076 | |||||||
chr22:42400085 | G | A | 4 | a0001c0001t0003g0218 a0001c0001t0003g0220 a0001c0001t0029g0206 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-2129C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400085 | |||||||
chr22:42400146 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-2190G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400146 | |||||||
chr22:42400247 | G | A | 1 | a0001c0003t0007g0355 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.565-2291C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400247 | |||||||
chr22:42400309 | A | C | 1 | a0001c0001t0009g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.565-2353T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400309 | |||||||
chr22:42400321 | G | A | 2 | a0001c0001t0032g0290 a0001c0003t0057g0175 |
2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.565-2365C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400321 | |||||||
chr22:42400407 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0026g0033 a0001c0001t0026g0264 others(11): Show |
19 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-2451G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400407 | |||||||
chr22:42400415 | C | T | 3 | a0001c0001t0001g0120 a0001c0003t0008g0256 a0003c0006t0016g0257 |
3 | HG03486.hp1 HG03834.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.565-2459G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400415 | |||||||
chr22:42400463 | C | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0185 a0001c0001t0001g0221 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-2507G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400463 | |||||||
chr22:42400510 | C | T | 21 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(18): Show |
21 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.565-2554G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400510 | |||||||
chr22:42400578 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | NA18975.hp2 NA18982.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-2622A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400578 | |||||||
chr22:42400737 | A | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0185 a0001c0001t0001g0221 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-2781T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400737 | |||||||
chr22:42400772 | A | T | 125 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0002g0003 others(122): Show |
133 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.565-2816T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400772 | |||||||
chr22:42400830 | T | C | 3 | a0001c0001t0005g0283 a0001c0001t0005g0284 a0001c0001t0056g0286 |
3 | HG00642.hp2 HG01256.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.565-2874A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400830 | |||||||
chr22:42400896 | A | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(112): Show |
121 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.565-2940T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400896 | |||||||
chr22:42400908 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(97): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.565-2952C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400908 | |||||||
chr22:42400955 | G | A | 11 | a0001c0001t0001g0058 a0001c0001t0001g0185 a0001c0001t0001g0221 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-2999C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42400955 | |||||||
chr22:42401026 | G | A | 1 | a0001c0001t0021g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.565-3070C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401026 | |||||||
chr22:42401199 | A | G | 1 | a0001c0001t0010g0208 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.565-3243T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401199 | |||||||
chr22:42401237 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-3281T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401237 | |||||||
chr22:42401361 | C | T | 9 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.565-3405G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401361 | |||||||
chr22:42401373 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.565-3417G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401373 | |||||||
chr22:42401376 | G | A | 1 | a0001c0001t0028g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.565-3420C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401376 | |||||||
chr22:42401399 | G | C | 4 | a0001c0001t0002g0293 a0001c0001t0002g0302 a0001c0001t0002g0315 others(1): Show |
4 | NA18971.hp1 NA18983.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-3443C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401399 | |||||||
chr22:42401490 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565-3534C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401490 | |||||||
chr22:42401535 | C | T | 15 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(12): Show |
15 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.565-3579G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401535 | |||||||
chr22:42401613 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0026g0033 a0001c0001t0026g0264 others(11): Show |
19 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-3657G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401613 | |||||||
chr22:42401639 | C | T | 1 | a0001c0001t0028g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.565-3683G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401639 | |||||||
chr22:42401673 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.565-3717G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401673 | |||||||
chr22:42401689 | A | C | 2 | a0001c0003t0007g0280 a0001c0003t0007g0346 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.565-3733T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401689 | |||||||
chr22:42401779 | A | G | 66 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(63): Show |
69 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.565-3823T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401779 | |||||||
chr22:42401980 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.565-4024C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42401980 | |||||||
chr22:42402020 | G | A | 1 | a0001c0001t0029g0206 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.565-4064C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402020 | |||||||
chr22:42402091 | T | C | 123 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(120): Show |
131 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.565-4135A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402091 | |||||||
chr22:42402151 | G | A | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.565-4195C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402151 | |||||||
chr22:42402176 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.565-4220G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402176 | |||||||
chr22:42402272 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-4316G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402272 | |||||||
chr22:42402464 | C | T | 6 | a0001c0001t0002g0035 a0004c0007t0005g0276 a0004c0007t0018g0358 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-4508G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402464 | |||||||
chr22:42402474 | C | G | 2 | a0001c0001t0010g0189 a0001c0001t0010g0190 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.565-4518G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402474 | |||||||
chr22:42402475 | G | C | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-4519C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402475 | |||||||
chr22:42402486 | C | A | 112 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(109): Show |
120 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.565-4530G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402486 | |||||||
chr22:42402565 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0253 a0001c0001t0002g0254 |
4 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.565-4609C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402565 | |||||||
chr22:42402593 | C | T | 1 | a0001c0001t0001g0004 | 2 | NA19009.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.565-4637G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402593 | |||||||
chr22:42402631 | T | C | 123 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(120): Show |
131 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.565-4675A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402631 | |||||||
chr22:42402638 | A | AGAGGAT | 31 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(28): Show |
33 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.565-4688_565-4683d others(8): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402638 | |||||||
chr22:42402666 | G | A | 5 | a0001c0005t0005g0079 a0001c0005t0005g0258 a0001c0005t0045g0260 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-4710C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402666 | |||||||
chr22:42402701 | C | A | 1 | a0001c0001t0011g0109 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.565-4745G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402701 | |||||||
chr22:42402775 | G | C | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.565-4819C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402775 | |||||||
chr22:42402831 | C | CT | 78 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0194 others(75): Show |
83 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.565-4876dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402831 | |||||||
chr22:42402831 | C | CTT | 92 | a0001c0001t0001g0216 a0001c0001t0002g0035 a0001c0001t0002g0308 others(89): Show |
94 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.565-4877_565-4876d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402831 | |||||||
chr22:42402831 | C | CTTCTT | 9 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.565-4876_565-4875i others(7): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402831 | |||||||
chr22:42402831 | C | CTTT | 17 | a0001c0001t0002g0003 a0001c0001t0003g0186 a0001c0001t0003g0201 others(14): Show |
22 | HG00673.hp1 HG01496.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.565-4878_565-4876d others(5): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402831 | |||||||
chr22:42402831 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0054g0298 |
3 | HG02622.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.565-4885_565-4876d others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402831 | |||||||
chr22:42402862 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.565-4906C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402862 | |||||||
chr22:42402979 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-5023T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402979 | |||||||
chr22:42402982 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.565-5026G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402982 | |||||||
chr22:42402991 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-5035A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402991 | |||||||
chr22:42402996 | G | A | 2 | a0001c0003t0007g0280 a0001c0003t0007g0346 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.565-5040C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42402996 | |||||||
chr22:42403077 | A | AT | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-5122_565-5121i others(3): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403077 | |||||||
chr22:42403092 | C | T | 32 | a0001c0001t0002g0320 a0001c0001t0005g0281 a0001c0001t0005g0282 others(29): Show |
34 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.565-5136G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403092 | |||||||
chr22:42403112 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-5156A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403112 | |||||||
chr22:42403162 | G | C | 6 | a0001c0001t0002g0035 a0004c0007t0005g0276 a0004c0007t0018g0358 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-5206C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403162 | |||||||
chr22:42403273 | C | T | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.565-5317G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403273 | |||||||
chr22:42403448 | T | C | 123 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(120): Show |
131 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.565-5492A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403448 | |||||||
chr22:42403474 | G | A | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-5518C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403474 | |||||||
chr22:42403505 | G | T | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.565-5549C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403505 | |||||||
chr22:42403617 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.565-5661G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403617 | |||||||
chr22:42403708 | G | A | 7 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(4): Show |
7 | HG02280.hp1 HG02976.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+5727C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403708 | |||||||
chr22:42403721 | G | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+5714C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403721 | |||||||
chr22:42403746 | C | T | 1 | a0001c0005t0005g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.564+5689G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403746 | |||||||
chr22:42403781 | C | T | 1 | a0001c0001t0051g0181 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.564+5654G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403781 | |||||||
chr22:42403819 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+5616C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403819 | |||||||
chr22:42403821 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+5614C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403821 | |||||||
chr22:42403870 | G | A | 60 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(57): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.564+5565C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403870 | |||||||
chr22:42403947 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+5488C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42403947 | |||||||
chr22:42404013 | T | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+5422A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404013 | |||||||
chr22:42404014 | G | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0118 others(2): Show |
5 | NA18940.hp2 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+5421C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404014 | |||||||
chr22:42404075 | C | T | 31 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(28): Show |
33 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.564+5360G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404075 | |||||||
chr22:42404087 | A | G | 6 | a0001c0001t0003g0277 a0001c0001t0005g0059 a0001c0001t0005g0060 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.564+5348T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404087 | |||||||
chr22:42404106 | C | G | 1 | a0001c0001t0004g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.564+5329G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404106 | |||||||
chr22:42404135 | G | A | 13 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0046 others(10): Show |
13 | HG02074.hp1 HG02135.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.564+5300C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404135 | |||||||
chr22:42404275 | C | T | 1 | a0003c0006t0016g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.564+5160G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404275 | |||||||
chr22:42404501 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.564+4934C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404501 | |||||||
chr22:42404585 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4850C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404585 | |||||||
chr22:42404614 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4821G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404614 | |||||||
chr22:42404712 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4723T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404712 | |||||||
chr22:42404815 | T | C | 14 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(11): Show |
14 | HG00639.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.564+4620A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404815 | |||||||
chr22:42404818 | T | C | 14 | a0001c0001t0003g0277 a0001c0001t0064g0262 a0001c0015t0003g0261 others(11): Show |
14 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.564+4617A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404818 | |||||||
chr22:42404852 | C | CA | 81 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0304 others(78): Show |
90 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.564+4582dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404852 | |||||||
chr22:42404852 | C | CAA | 36 | a0001c0001t0002g0326 a0001c0001t0005g0017 a0001c0001t0005g0021 others(33): Show |
36 | HG00621.hp2 HG00639.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.564+4581_564+4582d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404852 | |||||||
chr22:42404852 | CA | C | 12 | a0001c0001t0001g0068 a0001c0001t0001g0101 a0001c0001t0001g0155 others(9): Show |
12 | HG00323.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.564+4582delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404852 | |||||||
chr22:42404852 | CAAA | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4580_564+4582d others(5): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404852 | |||||||
chr22:42404920 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4515A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42404920 | |||||||
chr22:42405000 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4435A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405000 | |||||||
chr22:42405173 | T | C | 2 | a0001c0002t0012g0336 a0001c0002t0047g0289 |
2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.564+4262A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405173 | |||||||
chr22:42405341 | G | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4094C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405341 | |||||||
chr22:42405352 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4083G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405352 | |||||||
chr22:42405398 | G | A | 6 | a0001c0001t0003g0277 a0001c0001t0005g0059 a0001c0001t0005g0060 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.564+4037C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405398 | |||||||
chr22:42405446 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0216 others(226): Show |
243 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.564+3989T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405446 | |||||||
chr22:42405493 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3942T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405493 | |||||||
chr22:42405538 | GA | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3896delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405538 | |||||||
chr22:42405556 | A | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3879T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405556 | |||||||
chr22:42405587 | T | C | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.564+3848A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405587 | |||||||
chr22:42405612 | G | A | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+3823C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405612 | |||||||
chr22:42405738 | G | A | 1 | a0001c0012t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564+3697C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405738 | |||||||
chr22:42405773 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3662T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405773 | |||||||
chr22:42405799 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3636C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405799 | |||||||
chr22:42405973 | C | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3462G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405973 | |||||||
chr22:42405989 | C | A | 1 | a0006c0010t0006g0057 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.564+3446G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405989 | |||||||
chr22:42405995 | A | G | 1 | a0001c0001t0010g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.564+3440T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42405995 | |||||||
chr22:42406064 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3371G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406064 | |||||||
chr22:42406115 | TTCCAGTC others(35): Show |
T | 209 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(206): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.564+3278_564+3319d others(44): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406115 | |||||||
chr22:42406144 | G | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3291C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406144 | |||||||
chr22:42406148 | C | T | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.564+3287G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406148 | |||||||
chr22:42406153 | G | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3282C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406153 | |||||||
chr22:42406169 | C | G | 1 | a0001c0003t0008g0173 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.564+3266G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406169 | |||||||
chr22:42406170 | C | T | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.564+3265G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406170 | |||||||
chr22:42406179 | G | A | 60 | a0001c0001t0001g0216 a0001c0001t0003g0007 a0001c0001t0003g0009 others(57): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.564+3256C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406179 | |||||||
chr22:42406179 | G | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3256C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406179 | |||||||
chr22:42406188 | C | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3247G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406188 | |||||||
chr22:42406190 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3245G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406190 | |||||||
chr22:42406191 | G | A | 20 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(17): Show |
20 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.564+3244C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406191 | |||||||
chr22:42406215 | G | A | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.564+3220C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406215 | |||||||
chr22:42406261 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3174G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406261 | |||||||
chr22:42406271 | G | A | 1 | a0001c0002t0012g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.564+3164C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406271 | |||||||
chr22:42406283 | A | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3152T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406283 | |||||||
chr22:42406322 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3113G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406322 | |||||||
chr22:42406344 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+3091A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406344 | |||||||
chr22:42406671 | A | G | 1 | a0003c0006t0016g0257 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.564+2764T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406671 | |||||||
chr22:42406844 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.564+2591C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406844 | |||||||
chr22:42406920 | G | A | 8 | a0001c0002t0012g0014 a0001c0002t0012g0197 a0001c0002t0012g0198 others(5): Show |
9 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+2515C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406920 | |||||||
chr22:42406937 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.564+2498C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42406937 | |||||||
chr22:42407060 | C | G | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+2375G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407060 | |||||||
chr22:42407081 | C | CTTTT | 10 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.564+2350_564+2353d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407081 | |||||||
chr22:42407081 | CT | C | 18 | a0001c0001t0001g0185 a0001c0001t0003g0224 a0001c0001t0004g0026 others(15): Show |
18 | HG00323.hp2 HG01109.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.564+2353delA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407081 | |||||||
chr22:42407114 | G | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0216 a0001c0001t0001g0304 others(193): Show |
208 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.564+2321C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407114 | |||||||
chr22:42407118 | T | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+2317A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407118 | |||||||
chr22:42407120 | C | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(12): Show |
20 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.564+2315G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407120 | |||||||
chr22:42407125 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.564+2310C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407125 | |||||||
chr22:42407207 | G | C | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+2228C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407207 | |||||||
chr22:42407361 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.564+2074G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407361 | |||||||
chr22:42407371 | C | T | 3 | a0001c0001t0003g0277 a0001c0001t0064g0262 a0001c0015t0003g0261 |
3 | HG01243.hp1 HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.564+2064G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407371 | |||||||
chr22:42407428 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+2007C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407428 | |||||||
chr22:42407431 | T | G | 7 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(4): Show |
7 | HG02055.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+2004A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407431 | |||||||
chr22:42407488 | C | T | 5 | a0004c0007t0005g0276 a0004c0007t0018g0358 a0004c0007t0018g0360 others(2): Show |
5 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+1947G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407488 | |||||||
chr22:42407513 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+1922G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407513 | |||||||
chr22:42407559 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0216 others(194): Show |
209 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.564+1876A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407559 | |||||||
chr22:42407573 | G | A | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+1862C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407573 | |||||||
chr22:42407627 | C | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+1808G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407627 | |||||||
chr22:42407802 | C | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0185 a0001c0001t0001g0221 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.564+1633G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407802 | |||||||
chr22:42407803 | G | A | 112 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(109): Show |
120 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.564+1632C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407803 | |||||||
chr22:42407903 | C | CT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0005g0059 others(7): Show |
11 | HG00099.hp2 HG01109.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+1531dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407903 | |||||||
chr22:42407903 | CT | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0143 others(191): Show |
208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.564+1531delA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407903 | |||||||
chr22:42407903 | CTT | C | 10 | a0001c0001t0002g0254 a0001c0001t0002g0317 a0001c0001t0002g0318 others(7): Show |
10 | HG01256.hp1 HG02897.hp2 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.564+1530_564+1531d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407903 | |||||||
chr22:42407906 | T | C | 3 | a0001c0001t0003g0277 a0001c0001t0064g0262 a0001c0015t0003g0261 |
3 | HG01243.hp1 HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.564+1529A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407906 | |||||||
chr22:42407922 | T | G | 10 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.564+1513A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407922 | |||||||
chr22:42407993 | C | T | 2 | a0001c0003t0008g0163 a0001c0003t0057g0175 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.564+1442G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42407993 | |||||||
chr22:42408022 | C | A | 27 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(24): Show |
27 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.564+1413G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408022 | |||||||
chr22:42408100 | G | T | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+1335C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408100 | |||||||
chr22:42408142 | C | T | 5 | a0001c0005t0005g0079 a0001c0005t0005g0258 a0001c0005t0045g0260 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+1293G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408142 | |||||||
chr22:42408154 | A | G | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+1281T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408154 | |||||||
chr22:42408337 | T | A | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+1098A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408337 | |||||||
chr22:42408406 | G | A | 2 | a0001c0001t0003g0202 a0001c0001t0030g0203 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.564+1029C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408406 | |||||||
chr22:42408414 | G | C | 124 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(121): Show |
132 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.564+1021C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408414 | |||||||
chr22:42408436 | T | G | 15 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(12): Show |
20 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.564+999A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408436 | |||||||
chr22:42408459 | G | A | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.564+976C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408459 | |||||||
chr22:42408464 | G | A | 2 | a0001c0001t0028g0344 a0001c0001t0028g0345 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.564+971C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408464 | |||||||
chr22:42408625 | G | T | 1 | a0001c0001t0026g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+810C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408625 | |||||||
chr22:42408646 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.564+789G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408646 | |||||||
chr22:42408957 | C | CTGGAGGG others(5): Show |
1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.564+466_564+477dup others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42408957 | |||||||
chr22:42409012 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0043g0062 |
4 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+423G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409012 | |||||||
chr22:42409110 | G | A | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+325C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409110 | |||||||
chr22:42409161 | G | A | 1 | a0001c0001t0009g0075 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.564+274C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409161 | |||||||
chr22:42409198 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.564+237C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409198 | |||||||
chr22:42409244 | A | G | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+191T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409244 | |||||||
chr22:42409265 | T | C | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+170A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409265 | |||||||
chr22:42409298 | AG | A | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+136delC | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409298 | |||||||
chr22:42409306 | CG | C | 10 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.564+128delC | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409306 | |||||||
chr22:42409353 | C | T | 3 | a0001c0002t0004g0347 a0001c0003t0008g0256 a0003c0006t0016g0257 |
3 | HG02965.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.564+82G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409353 | |||||||
chr22:42409357 | C | T | 1 | a0001c0001t0060g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.564+78G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409357 | |||||||
chr22:42409430 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA19054.hp1 | splice_region_variant&intron_variant | LOW | c.564+5G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 3/5 | chr22 | 42409430 | |||||||
chr22:42409559 | C | T | 3 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0021g0089 |
3 | HG02056.hp2 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.452-12G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409559 | |||||||
chr22:42409649 | A | AC | 8 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0003g0202 others(5): Show |
8 | HG00673.hp2 HG01978.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-103dupG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409649 | |||||||
chr22:42409676 | T | C | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-129A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409676 | |||||||
chr22:42409732 | C | T | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-185G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409732 | |||||||
chr22:42409740 | C | T | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-193G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409740 | |||||||
chr22:42409828 | C | A | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.452-281G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409828 | |||||||
chr22:42409833 | C | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.452-286G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409833 | |||||||
chr22:42409851 | G | A | 1 | a0001c0001t0010g0275 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.452-304C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409851 | |||||||
chr22:42409889 | C | T | 117 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0035 others(114): Show |
125 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.452-342G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409889 | |||||||
chr22:42409919 | G | A | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.452-372C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409919 | |||||||
chr22:42409921 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0216 others(226): Show |
243 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.452-374T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42409921 | |||||||
chr22:42410020 | C | A | 2 | a0001c0001t0005g0059 a0001c0001t0005g0060 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.452-473G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410020 | |||||||
chr22:42410064 | G | A | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-517C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410064 | |||||||
chr22:42410118 | T | C | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.452-571A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410118 | |||||||
chr22:42410434 | C | T | 1 | a0001c0001t0043g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.452-887G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410434 | |||||||
chr22:42410457 | G | A | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-910C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410457 | |||||||
chr22:42410637 | T | C | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.451+770A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410637 | |||||||
chr22:42410658 | C | CA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0005g0025 others(7): Show |
10 | HG00639.hp2 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+748dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410658 | |||||||
chr22:42410658 | CA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0241 others(137): Show |
151 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.451+748delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410658 | |||||||
chr22:42410725 | A | C | 31 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(28): Show |
33 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.451+682T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410725 | |||||||
chr22:42410979 | C | G | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0118 others(2): Show |
5 | NA18940.hp2 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+428G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42410979 | |||||||
chr22:42411019 | C | CT | 58 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0067 others(55): Show |
64 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.451+387dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411019 | |||||||
chr22:42411019 | C | CTT | 16 | a0001c0001t0001g0116 a0001c0001t0004g0026 a0001c0001t0004g0028 others(13): Show |
16 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+386_451+387dup others(2): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411019 | |||||||
chr22:42411019 | CT | C | 9 | a0001c0001t0001g0064 a0001c0001t0001g0093 a0001c0001t0001g0126 others(6): Show |
9 | HG00609.hp2 HG01516.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+387delA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411019 | |||||||
chr22:42411019 | CTTTTTT | C | 26 | a0001c0003t0007g0161 a0001c0003t0007g0166 a0001c0003t0007g0168 others(23): Show |
26 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.451+382_451+387del others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411019 | |||||||
chr22:42411019 | CTTTTTTT | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0304 others(104): Show |
113 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.451+381_451+387del others(7): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411019 | |||||||
chr22:42411210 | G | C | 9 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(6): Show |
9 | HG00642.hp2 HG01256.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.451+197C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411210 | |||||||
chr22:42411308 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0304 others(130): Show |
144 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.451+99A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411308 | |||||||
chr22:42411316 | G | A | 27 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(24): Show |
32 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.451+91C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411316 | |||||||
chr22:42411345 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0304 others(103): Show |
112 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.451+62G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411345 | |||||||
chr22:42411395 | A | G | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.451+12T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 2/5 | chr22 | 42411395 | |||||||
chr22:42411825 | C | T | 1 | a0001c0002t0004g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-89G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42411825 | |||||||
chr22:42411864 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0304 others(103): Show |
112 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.122-128C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42411864 | |||||||
chr22:42412209 | G | A | 10 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-473C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412209 | |||||||
chr22:42412221 | A | G | 2 | a0001c0001t0003g0096 a0001c0001t0003g0098 |
2 | NA19005.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.122-485T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412221 | |||||||
chr22:42412308 | G | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-572C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412308 | |||||||
chr22:42412395 | C | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(12): Show |
20 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-659G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412395 | |||||||
chr22:42412423 | G | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(12): Show |
20 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-687C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412423 | |||||||
chr22:42412529 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.122-793A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412529 | |||||||
chr22:42412530 | T | C | 110 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0001t0001g0216 others(107): Show |
115 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.122-794A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412530 | |||||||
chr22:42412657 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.122-921C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412657 | |||||||
chr22:42412756 | GCTCGGAG others(21): Show |
G | 1 | a0001c0001t0019g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.122-1048_122-1021d others(30): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412756 | |||||||
chr22:42412784 | C | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0004g0026 others(39): Show |
47 | HG01433.hp1 HG01496.hp2 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.122-1048G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412784 | |||||||
chr22:42412890 | A | C | 1 | a0001c0001t0050g0156 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.122-1154T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412890 | |||||||
chr22:42412961 | C | T | 3 | a0001c0001t0019g0081 a0001c0001t0019g0082 a0001c0001t0019g0083 |
3 | NA18957.hp2 NA18961.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.122-1225G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42412961 | |||||||
chr22:42413104 | G | A | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-1368C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413104 | |||||||
chr22:42413182 | G | A | 5 | a0004c0007t0005g0276 a0004c0007t0018g0358 a0004c0007t0018g0360 others(2): Show |
5 | HG00639.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-1446C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413182 | |||||||
chr22:42413261 | T | C | 28 | a0001c0001t0001g0155 a0001c0001t0002g0003 a0001c0001t0002g0035 others(25): Show |
33 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.122-1525A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413261 | |||||||
chr22:42413391 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.122-1655C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413391 | |||||||
chr22:42413546 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00280.hp1 HG01123.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1810G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413546 | |||||||
chr22:42413547 | G | A | 1 | a0001c0003t0007g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122-1811C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413547 | |||||||
chr22:42413607 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.122-1871G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413607 | |||||||
chr22:42413860 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(232): Show |
249 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.122-2124A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413860 | |||||||
chr22:42413957 | G | A | 1 | a0001c0001t0005g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.122-2221C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42413957 | |||||||
chr22:42414047 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(70): Show |
77 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.122-2311A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414047 | |||||||
chr22:42414082 | A | G | 102 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0221 others(99): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.122-2346T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414082 | |||||||
chr22:42414213 | A | G | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-2477T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414213 | |||||||
chr22:42414242 | G | A | 102 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0221 others(99): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.122-2506C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414242 | |||||||
chr22:42414295 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(200): Show |
215 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.122-2559G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414295 | |||||||
chr22:42414305 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.122-2569A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414305 | |||||||
chr22:42414389 | G | A | 2 | a0004c0007t0018g0360 a0005c0014t0005g0027 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.122-2653C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414389 | |||||||
chr22:42414557 | A | AT | 11 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(8): Show |
11 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.122-2822dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414557 | |||||||
chr22:42414557 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.122-2821T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414557 | |||||||
chr22:42414583 | T | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(94): Show |
100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.122-2847A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414583 | |||||||
chr22:42414634 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122-2898G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414634 | |||||||
chr22:42414708 | G | A | 1 | a0001c0003t0057g0175 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.122-2972C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414708 | |||||||
chr22:42414963 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.122-3227C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414963 | |||||||
chr22:42414982 | G | A | 64 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0221 others(61): Show |
67 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.122-3246C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42414982 | |||||||
chr22:42415004 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.122-3268G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415004 | |||||||
chr22:42415070 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(35): Show |
40 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.122-3334G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415070 | |||||||
chr22:42415095 | C | T | 64 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0221 others(61): Show |
67 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.122-3359G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415095 | |||||||
chr22:42415150 | A | G | 14 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(11): Show |
14 | HG00642.hp2 HG01109.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-3414T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415150 | |||||||
chr22:42415156 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(201): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.122-3420A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415156 | |||||||
chr22:42415170 | G | A | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-3434C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415170 | |||||||
chr22:42415184 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.122-3448G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415184 | |||||||
chr22:42415187 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.122-3451C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415187 | |||||||
chr22:42415261 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.122-3525G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415261 | |||||||
chr22:42415294 | C | CT | 12 | a0001c0001t0001g0100 a0001c0001t0001g0151 a0001c0001t0003g0224 others(9): Show |
12 | HG00639.hp2 HG01192.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-3559dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415294 | |||||||
chr22:42415294 | C | CTT | 11 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.122-3560_122-3559d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415294 | |||||||
chr22:42415294 | CT | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0147 others(142): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.122-3559delA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415294 | |||||||
chr22:42415294 | CTT | C | 13 | a0001c0001t0001g0306 a0001c0001t0002g0296 a0001c0001t0002g0322 others(10): Show |
13 | HG01891.hp2 HG02257.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-3560_122-3559d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415294 | |||||||
chr22:42415294 | CTTTTTTT others(8): Show |
C | 1 | a0002c0004t0003g0348 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122-3573_122-3559d others(17): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415294 | |||||||
chr22:42415396 | T | G | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-3660A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415396 | |||||||
chr22:42415453 | C | A | 1 | a0001c0012t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.122-3717G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415453 | |||||||
chr22:42415460 | T | C | 27 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(24): Show |
32 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.122-3724A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415460 | |||||||
chr22:42415463 | C | A | 1 | a0001c0001t0002g0291 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.122-3727G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415463 | |||||||
chr22:42415500 | C | T | 2 | a0001c0003t0008g0256 a0003c0006t0016g0257 |
2 | HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.122-3764G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415500 | |||||||
chr22:42415535 | G | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0033 others(12): Show |
20 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-3799C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415535 | |||||||
chr22:42415567 | G | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0250 |
2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.122-3831C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415567 | |||||||
chr22:42415584 | C | T | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-3848G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415584 | |||||||
chr22:42415591 | G | A | 12 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-3855C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415591 | |||||||
chr22:42415641 | A | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(201): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.122-3905T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415641 | |||||||
chr22:42415642 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(201): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.122-3906A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415642 | |||||||
chr22:42415774 | G | A | 1 | a0001c0001t0028g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.122-4038C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415774 | |||||||
chr22:42415790 | G | A | 1 | a0001c0001t0022g0279 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-4054C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415790 | |||||||
chr22:42415873 | A | G | 1 | a0001c0001t0002g0303 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.122-4137T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415873 | |||||||
chr22:42415892 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-4156C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415892 | |||||||
chr22:42415897 | G | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-4161C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415897 | |||||||
chr22:42415913 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(71): Show |
78 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.122-4177T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42415913 | |||||||
chr22:42416022 | G | A | 1 | a0001c0001t0036g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.122-4286C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416022 | |||||||
chr22:42416035 | G | A | 68 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0221 others(65): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.122-4299C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416035 | |||||||
chr22:42416087 | C | T | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-4351G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416087 | |||||||
chr22:42416363 | G | A | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-4627C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416363 | |||||||
chr22:42416412 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-4676C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416412 | |||||||
chr22:42416424 | A | G | 14 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0004t0003g0348 others(11): Show |
14 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-4688T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416424 | |||||||
chr22:42416465 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0116 a0001c0001t0001g0155 others(235): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.122-4729T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416465 | |||||||
chr22:42416466 | T | G | 136 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0001t0001g0216 others(133): Show |
144 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.122-4730A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416466 | |||||||
chr22:42416731 | A | T | 1 | a0001c0001t0002g0328 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.122-4995T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416731 | |||||||
chr22:42416747 | C | T | 6 | a0001c0001t0022g0278 a0001c0001t0022g0279 a0001c0008t0004g0363 others(3): Show |
6 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-5011G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416747 | |||||||
chr22:42416814 | G | T | 2 | a0001c0002t0012g0336 a0001c0002t0047g0289 |
2 | HG00733.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.122-5078C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416814 | |||||||
chr22:42416927 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-5191C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416927 | |||||||
chr22:42416943 | G | A | 10 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-5207C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42416943 | |||||||
chr22:42417036 | G | C | 116 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0001t0001g0193 others(113): Show |
119 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.122-5300C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417036 | |||||||
chr22:42417054 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.122-5318G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417054 | |||||||
chr22:42417105 | G | A | 14 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0004t0003g0348 others(11): Show |
14 | HG02280.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-5369C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417105 | |||||||
chr22:42417147 | A | G | 3 | a0001c0001t0005g0059 a0001c0001t0005g0060 a0001c0001t0054g0298 |
3 | HG02622.hp1 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122-5411T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417147 | |||||||
chr22:42417150 | C | G | 131 | a0001c0001t0001g0155 a0001c0001t0001g0185 a0001c0001t0001g0193 others(128): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.122-5414G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417150 | |||||||
chr22:42417323 | G | T | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.122-5587C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417323 | |||||||
chr22:42417345 | C | T | 2 | a0001c0001t0024g0090 a0001c0001t0024g0095 |
2 | NA18964.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.122-5609G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417345 | |||||||
chr22:42417439 | T | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-5703A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417439 | |||||||
chr22:42417457 | A | G | 1 | a0001c0001t0002g0310 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.122-5721T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417457 | |||||||
chr22:42417493 | GGAACGGA others(5): Show |
G | 31 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(28): Show |
33 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.122-5769_122-5758d others(14): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417493 | |||||||
chr22:42417497 | C | T | 34 | a0001c0001t0001g0155 a0001c0001t0003g0277 a0001c0001t0004g0026 others(31): Show |
34 | HG01243.hp1 HG01433.hp1 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.122-5761G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417497 | |||||||
chr22:42417527 | A | G | 4 | a0004c0007t0018g0358 a0004c0007t0018g0360 a0004c0007t0018g0361 others(1): Show |
4 | HG00639.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-5791T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417527 | |||||||
chr22:42417649 | C | G | 10 | a0002c0004t0003g0348 a0002c0004t0013g0077 a0002c0004t0013g0234 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.122-5913G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417649 | |||||||
chr22:42417728 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-5992A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417728 | |||||||
chr22:42417747 | T | C | 108 | a0001c0001t0001g0088 a0001c0001t0001g0155 a0001c0001t0001g0185 others(105): Show |
115 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.122-6011A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417747 | |||||||
chr22:42417756 | G | A | 4 | a0001c0001t0003g0277 a0001c0001t0064g0262 a0001c0015t0003g0261 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6020C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417756 | |||||||
chr22:42417788 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.122-6052C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417788 | |||||||
chr22:42417823 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.122-6087G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417823 | |||||||
chr22:42417904 | T | A | 1 | a0004c0007t0018g0360 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122-6168A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417904 | |||||||
chr22:42417905 | C | A | 1 | a0004c0007t0018g0360 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122-6169G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417905 | |||||||
chr22:42417976 | G | A | 4 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-6240C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42417976 | |||||||
chr22:42418021 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG00140.hp1 HG00323.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6285C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418021 | |||||||
chr22:42418625 | G | A | 4 | a0003c0006t0016g0032 a0003c0006t0016g0182 a0003c0006t0016g0183 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6889C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418625 | |||||||
chr22:42418688 | G | GT | 7 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0064g0262 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-6953dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418688 | |||||||
chr22:42418688 | G | T | 3 | a0001c0001t0002g0288 a0001c0001t0002g0332 a0001c0001t0002g0343 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.122-6952C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418688 | |||||||
chr22:42418735 | C | T | 4 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-6999G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418735 | |||||||
chr22:42418850 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.122-7114C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42418850 | |||||||
chr22:42419048 | G | C | 1 | a0001c0002t0004g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-7312C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419048 | |||||||
chr22:42419101 | G | A | 1 | a0001c0001t0036g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.122-7365C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419101 | |||||||
chr22:42419112 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-7376A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419112 | |||||||
chr22:42419119 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(126): Show |
138 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.122-7383C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419119 | |||||||
chr22:42419131 | G | A | 2 | a0001c0001t0010g0189 a0001c0001t0010g0190 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.122-7395C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419131 | |||||||
chr22:42419207 | C | T | 2 | a0001c0001t0003g0202 a0001c0001t0030g0203 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122-7471G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419207 | |||||||
chr22:42419276 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-7540C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419276 | |||||||
chr22:42419292 | C | T | 14 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0017g0019 others(11): Show |
19 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-7556G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419292 | |||||||
chr22:42419352 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(141): Show |
153 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.122-7616C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419352 | |||||||
chr22:42419433 | G | A | 1 | a0001c0001t0019g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.122-7697C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419433 | |||||||
chr22:42419458 | T | C | 2 | a0001c0002t0012g0197 a0001c0002t0012g0198 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.122-7722A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419458 | |||||||
chr22:42419588 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122-7852C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419588 | |||||||
chr22:42419639 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-7903A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419639 | |||||||
chr22:42419750 | C | G | 70 | a0001c0001t0001g0088 a0001c0001t0001g0185 a0001c0001t0001g0193 others(67): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.122-8014G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419750 | |||||||
chr22:42419802 | G | A | 6 | a0001c0001t0002g0297 a0001c0001t0002g0362 a0003c0006t0016g0032 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-8066C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419802 | |||||||
chr22:42419802 | G | T | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-8066C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419802 | |||||||
chr22:42419818 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0132 others(1): Show |
4 | HG01099.hp2 HG01175.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-8082G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419818 | |||||||
chr22:42419855 | A | G | 4 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-8119T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419855 | |||||||
chr22:42419957 | C | T | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-8221G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419957 | |||||||
chr22:42419988 | TG | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0068 others(27): Show |
31 | HG00280.hp1 HG01099.hp2 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.122-8253delC | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419988 | |||||||
chr22:42419989 | G | GT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0085 others(21): Show |
24 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.122-8254_122-8253i others(3): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | G | GTT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0100 a0001c0001t0001g0147 others(4): Show |
7 | HG01106.hp1 HG01255.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-8254_122-8253i others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTT | G | 10 | a0001c0001t0005g0281 a0001c0001t0005g0283 a0001c0001t0005g0284 others(7): Show |
10 | HG00642.hp2 HG01256.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-8259_122-8254d others(8): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT | G | 38 | a0001c0001t0002g0266 a0001c0001t0002g0291 a0001c0001t0002g0307 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.122-8260_122-8254d others(9): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(1): Show |
G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0001g0185 others(156): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.122-8261_122-8254d others(10): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(2): Show |
G | 47 | a0001c0001t0001g0155 a0001c0001t0002g0254 a0001c0001t0002g0296 others(44): Show |
49 | HG00099.hp1 HG00733.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.122-8262_122-8254d others(11): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(3): Show |
G | 6 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0005g0357 others(3): Show |
6 | HG00639.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-8263_122-8254d others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(4): Show |
G | 1 | a0001c0001t0005g0356 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.122-8264_122-8254d others(13): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.122-8267_122-8254d others(16): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(9): Show |
G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0334 |
3 | HG04204.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.122-8269_122-8254d others(18): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419989 | GGTTTTTT others(10): Show |
G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0028 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.122-8270_122-8254d others(19): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419989 | |||||||
chr22:42419990 | G | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0038 others(64): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.122-8254C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419990 | |||||||
chr22:42419998 | T | G | 1 | a0001c0001t0054g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122-8262A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419998 | |||||||
chr22:42419999 | T | G | 13 | a0001c0001t0002g0266 a0001c0001t0002g0291 a0001c0001t0002g0307 others(10): Show |
13 | HG00438.hp1 HG02074.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-8263A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42419999 | |||||||
chr22:42420000 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(72): Show |
79 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.122-8264A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420000 | |||||||
chr22:42420001 | T | G | 28 | a0001c0001t0002g0254 a0001c0001t0002g0296 a0001c0001t0002g0301 others(25): Show |
28 | HG00099.hp1 HG01167.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-8265A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420001 | |||||||
chr22:42420002 | T | G | 1 | a0001c0001t0025g0036 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.122-8266A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420002 | |||||||
chr22:42420003 | T | G | 1 | a0001c0001t0025g0037 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.122-8267A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420003 | |||||||
chr22:42420013 | T | G | 58 | a0001c0001t0001g0088 a0001c0001t0001g0185 a0001c0001t0001g0193 others(55): Show |
58 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.122-8277A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420013 | |||||||
chr22:42420014 | T | G | 1 | a0001c0003t0007g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122-8278A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420014 | |||||||
chr22:42420020 | T | G | 1 | a0001c0001t0064g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.122-8284A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420020 | |||||||
chr22:42420026 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.122-8290A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420026 | |||||||
chr22:42420059 | C | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0026g0264 others(10): Show |
18 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-8323G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420059 | |||||||
chr22:42420060 | G | A | 20 | a0001c0001t0001g0155 a0001c0001t0005g0025 a0001c0001t0038g0364 others(17): Show |
22 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.122-8324C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420060 | |||||||
chr22:42420245 | G | C | 2 | a0001c0003t0007g0177 a0001c0003t0007g0178 |
2 | HG01934.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.122-8509C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420245 | |||||||
chr22:42420267 | T | A | 13 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0046 others(10): Show |
13 | HG02074.hp1 HG02135.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-8531A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420267 | |||||||
chr22:42420329 | C | T | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-8593G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420329 | |||||||
chr22:42420462 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(51): Show |
56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.122-8726T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420462 | |||||||
chr22:42420464 | C | G | 1 | a0001c0001t0026g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122-8728G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420464 | |||||||
chr22:42420501 | C | T | 16 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(13): Show |
16 | HG02074.hp1 HG02083.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.122-8765G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420501 | |||||||
chr22:42420536 | C | T | 19 | a0001c0001t0005g0025 a0001c0001t0038g0364 a0001c0001t0062g0352 others(16): Show |
21 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-8800G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420536 | |||||||
chr22:42420542 | G | C | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-8806C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420542 | |||||||
chr22:42420658 | C | T | 19 | a0001c0001t0005g0025 a0001c0001t0038g0364 a0001c0001t0062g0352 others(16): Show |
21 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-8922G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420658 | |||||||
chr22:42420706 | C | T | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-8970G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420706 | |||||||
chr22:42420711 | A | C | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-8975T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420711 | |||||||
chr22:42420721 | A | G | 99 | a0001c0001t0001g0088 a0001c0001t0001g0185 a0001c0001t0001g0193 others(96): Show |
106 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.122-8985T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420721 | |||||||
chr22:42420756 | CGAGA | C | 28 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0005g0281 others(25): Show |
33 | HG00642.hp2 HG01109.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.122-9024_122-9021d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420756 | |||||||
chr22:42420757 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.122-9021C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420757 | |||||||
chr22:42420973 | T | C | 21 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(18): Show |
21 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.122-9237A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42420973 | |||||||
chr22:42421021 | C | A | 7 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(4): Show |
7 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-9285G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421021 | |||||||
chr22:42421037 | A | G | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.122-9301T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421037 | |||||||
chr22:42421086 | C | T | 28 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0006g0042 others(25): Show |
28 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-9350G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421086 | |||||||
chr22:42421197 | T | TC | 118 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0295 others(115): Show |
122 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.122-9462dupG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421197 | |||||||
chr22:42421220 | G | A | 66 | a0001c0001t0001g0088 a0001c0001t0001g0185 a0001c0001t0001g0193 others(63): Show |
68 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.122-9484C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421220 | |||||||
chr22:42421445 | C | CA | 114 | a0001c0001t0001g0088 a0001c0001t0001g0130 a0001c0001t0001g0185 others(111): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.122-9710dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421445 | |||||||
chr22:42421445 | C | CAA | 7 | a0001c0001t0005g0283 a0001c0001t0005g0284 a0001c0001t0006g0144 others(4): Show |
7 | HG00642.hp2 HG01256.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-9711_122-9710d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421445 | |||||||
chr22:42421445 | CA | C | 30 | a0001c0001t0001g0093 a0001c0001t0003g0094 a0001c0001t0004g0026 others(27): Show |
32 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.122-9710delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421445 | |||||||
chr22:42421646 | T | G | 117 | a0001c0001t0001g0088 a0001c0001t0001g0155 a0001c0001t0001g0185 others(114): Show |
124 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.122-9910A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421646 | |||||||
chr22:42421660 | C | T | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-9924G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421660 | |||||||
chr22:42421786 | T | C | 9 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(6): Show |
9 | HG00642.hp2 HG01256.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-10050A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421786 | |||||||
chr22:42421879 | C | CTGTTGGT others(4): Show |
258 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(255): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.122-10144_122-1014 others(15): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421879 | |||||||
chr22:42421919 | G | A | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.122-10183C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421919 | |||||||
chr22:42421982 | G | A | 3 | a0001c0001t0002g0288 a0001c0001t0002g0332 a0001c0001t0002g0343 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.122-10246C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42421982 | |||||||
chr22:42422013 | G | C | 1 | a0001c0001t0054g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121+10224C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422013 | |||||||
chr22:42422080 | C | T | 3 | a0001c0008t0040g0365 a0002c0009t0020g0366 a0002c0009t0020g0367 |
3 | HG02486.hp1 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.121+10157G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422080 | |||||||
chr22:42422327 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.121+9910G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422327 | |||||||
chr22:42422328 | G | A | 2 | a0001c0001t0011g0041 a0001c0001t0011g0131 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.121+9909C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422328 | |||||||
chr22:42422412 | A | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(255): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.121+9825T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422412 | |||||||
chr22:42422444 | A | G | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.121+9793T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422444 | |||||||
chr22:42422477 | G | A | 1 | a0001c0001t0002g0297 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.121+9760C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422477 | |||||||
chr22:42422492 | G | A | 17 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(14): Show |
19 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.121+9745C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422492 | |||||||
chr22:42422522 | T | A | 1 | a0002c0004t0013g0237 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.121+9715A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422522 | |||||||
chr22:42422531 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.121+9706C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422531 | |||||||
chr22:42422548 | C | T | 1 | a0001c0001t0015g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.121+9689G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422548 | |||||||
chr22:42422564 | C | T | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121+9673G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422564 | |||||||
chr22:42422565 | A | G | 1 | a0005c0014t0005g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.121+9672T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422565 | |||||||
chr22:42422674 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.121+9563G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422674 | |||||||
chr22:42422735 | T | C | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.121+9502A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422735 | |||||||
chr22:42422736 | C | G | 23 | a0001c0001t0001g0155 a0001c0001t0006g0042 a0001c0001t0006g0043 others(20): Show |
23 | HG01433.hp1 HG02074.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+9501G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422736 | |||||||
chr22:42422834 | G | T | 1 | a0001c0001t0005g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121+9403C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422834 | |||||||
chr22:42422922 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG00597.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.121+9315C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422922 | |||||||
chr22:42422956 | T | C | 1 | a0001c0001t0003g0224 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.121+9281A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422956 | |||||||
chr22:42422971 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(255): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.121+9266A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42422971 | |||||||
chr22:42423112 | C | CAAAAAAA others(1): Show |
79 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0194 others(76): Show |
82 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.121+9117_121+9124d others(10): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423112 | |||||||
chr22:42423112 | C | CAAAAAAA others(2): Show |
157 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0195 others(154): Show |
166 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.121+9116_121+9124d others(11): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423112 | |||||||
chr22:42423112 | C | CAAAAAAA others(3): Show |
17 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0001t0002g0327 others(14): Show |
18 | HG00438.hp1 HG00621.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.121+9115_121+9124d others(12): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423112 | |||||||
chr22:42423112 | C | CAAAAAAA others(4): Show |
1 | a0001c0005t0045g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.121+9114_121+9124d others(13): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423112 | |||||||
chr22:42423149 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0185 others(247): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.121+9088T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423149 | |||||||
chr22:42423331 | C | T | 1 | a0001c0001t0028g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121+8906G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423331 | |||||||
chr22:42423549 | T | TTAAATAA others(9): Show |
1 | a0001c0005t0005g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121+8687_121+8688i others(18): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423549 | |||||||
chr22:42423549 | T | TTAAATAA others(17): Show |
4 | a0001c0005t0005g0079 a0001c0005t0045g0260 a0001c0005t0048g0259 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+8687_121+8688i others(26): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423549 | |||||||
chr22:42423550 | G | GAAATAAA others(9): Show |
11 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0043g0062 others(8): Show |
16 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+8671_121+8686d others(18): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423550 | |||||||
chr22:42423550 | G | GAAATAAA others(17): Show |
12 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(9): Show |
12 | HG00642.hp2 HG01256.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.121+8686_121+8687i others(26): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423550 | |||||||
chr22:42423550 | G | T | 5 | a0001c0005t0005g0079 a0001c0005t0005g0258 a0001c0005t0045g0260 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+8687C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423550 | |||||||
chr22:42423630 | G | A | 4 | a0004c0007t0018g0358 a0004c0007t0018g0360 a0004c0007t0018g0361 others(1): Show |
4 | HG00639.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+8607C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423630 | |||||||
chr22:42423725 | C | CT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0295 others(112): Show |
124 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.121+8511dupA | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423725 | |||||||
chr22:42423725 | C | CTT | 85 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0194 others(82): Show |
89 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.121+8510_121+8511d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423725 | |||||||
chr22:42423747 | G | A | 18 | a0001c0001t0062g0352 a0001c0002t0004g0013 a0001c0002t0004g0024 others(15): Show |
20 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.121+8490C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423747 | |||||||
chr22:42423821 | A | G | 6 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+8416T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42423821 | |||||||
chr22:42424153 | T | C | 13 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0004g0030 others(10): Show |
13 | HG01433.hp1 HG02074.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+8084A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424153 | |||||||
chr22:42424201 | G | A | 8 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(5): Show |
8 | HG00642.hp2 HG01256.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.121+8036C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424201 | |||||||
chr22:42424225 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01123.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.121+8012G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424225 | |||||||
chr22:42424244 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0295 others(181): Show |
195 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.121+7993G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424244 | |||||||
chr22:42424258 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(138): Show |
151 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.121+7979T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424258 | |||||||
chr22:42424284 | A | G | 5 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+7953T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424284 | |||||||
chr22:42424332 | G | A | 5 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+7905C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424332 | |||||||
chr22:42424339 | A | C | 2 | a0001c0001t0021g0089 a0001c0001t0063g0199 |
2 | HG01993.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.121+7898T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424339 | |||||||
chr22:42424347 | A | G | 89 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0001g0086 others(86): Show |
91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.121+7890T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424347 | |||||||
chr22:42424358 | T | C | 2 | a0002c0009t0020g0366 a0002c0009t0020g0367 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.121+7879A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424358 | |||||||
chr22:42424414 | C | CA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(86): Show |
95 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.121+7822dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424414 | |||||||
chr22:42424420 | AG | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(11): Show |
14 | HG00642.hp2 HG01256.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+7816delC | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424420 | |||||||
chr22:42424421 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0155 others(181): Show |
195 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.121+7816C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424421 | |||||||
chr22:42424593 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA19007.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.121+7644A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424593 | |||||||
chr22:42424714 | T | G | 4 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+7523A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424714 | |||||||
chr22:42424892 | CCTTT | C | 5 | a0001c0001t0001g0141 a0001c0001t0009g0034 a0001c0001t0009g0074 others(2): Show |
5 | HG00408.hp2 HG02027.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+7341_121+7344d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424892 | |||||||
chr22:42424906 | T | C | 3 | a0004c0007t0018g0358 a0004c0007t0018g0360 a0004c0007t0018g0361 |
3 | HG00639.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.121+7331A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424906 | |||||||
chr22:42424911 | G | GTATT | 13 | a0001c0001t0001g0240 a0001c0002t0012g0014 a0001c0002t0012g0197 others(10): Show |
14 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+7322_121+7325d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | G | GTATTTAT others(1): Show |
77 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0295 others(74): Show |
81 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.121+7318_121+7325d others(10): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | G | GTATTTAT others(5): Show |
19 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(16): Show |
19 | HG02074.hp1 HG02083.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.121+7314_121+7325d others(14): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | G | GTATTTAT others(9): Show |
6 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+7310_121+7325d others(18): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | G | GTATTTAT others(13): Show |
4 | a0002c0004t0023g0076 a0002c0004t0023g0354 a0004c0007t0018g0358 others(1): Show |
4 | HG00639.hp2 HG02896.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+7306_121+7325d others(22): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | G | GTATTTAT others(17): Show |
1 | a0004c0007t0018g0360 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.121+7302_121+7325d others(26): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42424911 | GTATT | G | 40 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0010g0176 others(37): Show |
45 | HG00099.hp1 HG00735.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.121+7322_121+7325d others(6): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42424911 | |||||||
chr22:42425041 | C | A | 13 | a0001c0001t0017g0359 a0001c0001t0062g0352 a0001c0002t0004g0340 others(10): Show |
14 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+7196G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425041 | |||||||
chr22:42425121 | C | A | 3 | a0004c0007t0018g0358 a0004c0007t0018g0360 a0004c0007t0018g0361 |
3 | HG00639.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.121+7116G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425121 | |||||||
chr22:42425179 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0155 others(195): Show |
209 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.121+7058G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425179 | |||||||
chr22:42425271 | TC | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0295 others(104): Show |
112 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.121+6965delG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425271 | |||||||
chr22:42425289 | C | G | 1 | a0001c0005t0021g0239 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.121+6948G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425289 | |||||||
chr22:42425495 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0155 others(199): Show |
213 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.121+6742T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425495 | |||||||
chr22:42425531 | T | C | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+6706A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425531 | |||||||
chr22:42425572 | C | T | 1 | a0001c0001t0054g0298 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121+6665G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425572 | |||||||
chr22:42425692 | C | T | 13 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(10): Show |
13 | HG00642.hp2 HG01256.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+6545G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425692 | |||||||
chr22:42425722 | C | T | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.121+6515G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425722 | |||||||
chr22:42425723 | G | A | 1 | a0001c0001t0002g0339 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.121+6514C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425723 | |||||||
chr22:42425832 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121+6405G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425832 | |||||||
chr22:42425875 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.121+6362C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425875 | |||||||
chr22:42425886 | C | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+6351G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425886 | |||||||
chr22:42425886 | C | T | 4 | a0001c0008t0004g0363 a0001c0008t0040g0365 a0002c0009t0020g0366 others(1): Show |
4 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+6351G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425886 | |||||||
chr22:42425994 | A | G | 18 | a0001c0001t0017g0359 a0001c0001t0028g0344 a0001c0001t0028g0345 others(15): Show |
20 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.121+6243T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425994 | |||||||
chr22:42425995 | CAG | C | 20 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(17): Show |
20 | HG00642.hp2 HG01256.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.121+6240_121+6241d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42425995 | |||||||
chr22:42426129 | G | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+6108C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426129 | |||||||
chr22:42426189 | G | C | 45 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(42): Show |
47 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.121+6048C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426189 | |||||||
chr22:42426235 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.121+6002C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426235 | |||||||
chr22:42426252 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.121+5985A>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426252 | |||||||
chr22:42426258 | C | A | 2 | a0001c0001t0025g0036 a0001c0001t0025g0037 |
2 | HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.121+5979G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426258 | |||||||
chr22:42426277 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0155 others(199): Show |
213 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.121+5960A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426277 | |||||||
chr22:42426412 | G | A | 3 | a0004c0007t0018g0358 a0004c0007t0018g0360 a0004c0007t0018g0361 |
3 | HG00639.hp2 HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.121+5825C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426412 | |||||||
chr22:42426472 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0009g0146 |
2 | HG02040.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.121+5765A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426472 | |||||||
chr22:42426526 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.121+5711G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426526 | |||||||
chr22:42426553 | C | T | 1 | a0001c0003t0042g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.121+5684G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426553 | |||||||
chr22:42426673 | G | A | 48 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(45): Show |
50 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.121+5564C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426673 | |||||||
chr22:42426800 | C | T | 1 | a0001c0001t0026g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+5437G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426800 | |||||||
chr22:42426937 | T | G | 9 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+5300A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426937 | |||||||
chr22:42426986 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.121+5251C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426986 | |||||||
chr22:42426991 | G | A | 1 | a0004c0017t0052g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+5246C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42426991 | |||||||
chr22:42427069 | G | T | 1 | a0001c0001t0015g0078 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.121+5168C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427069 | |||||||
chr22:42427076 | C | T | 1 | a0001c0002t0004g0340 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.121+5161G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427076 | |||||||
chr22:42427134 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01123.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.121+5103G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427134 | |||||||
chr22:42427319 | G | A | 1 | a0001c0001t0002g0337 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.121+4918C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427319 | |||||||
chr22:42427490 | C | T | 6 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4747G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427490 | |||||||
chr22:42427493 | G | A | 2 | a0001c0001t0002g0149 a0001c0016t0002g0148 |
2 | HG01255.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.121+4744C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427493 | |||||||
chr22:42427548 | T | C | 2 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
2 | HG02683.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.121+4689A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427548 | |||||||
chr22:42427567 | T | C | 19 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(16): Show |
19 | HG00642.hp2 HG01256.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.121+4670A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427567 | |||||||
chr22:42427729 | G | A | 1 | a0001c0001t0002g0338 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.121+4508C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427729 | |||||||
chr22:42427742 | A | ATACACAC others(2): Show |
9 | a0002c0004t0013g0077 a0002c0004t0013g0234 a0002c0004t0013g0235 others(6): Show |
9 | HG02280.hp1 HG02572.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+4486_121+4494d others(11): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427742 | |||||||
chr22:42427806 | G | C | 1 | a0001c0005t0055g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.121+4431C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427806 | |||||||
chr22:42427910 | G | A | 56 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0194 others(53): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.121+4327C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42427910 | |||||||
chr22:42428030 | G | GAT | 4 | a0001c0001t0017g0359 a0004c0007t0018g0358 a0004c0007t0018g0360 others(1): Show |
4 | HG00639.hp2 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+4205_121+4206d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428030 | |||||||
chr22:42428088 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.121+4149C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428088 | |||||||
chr22:42428252 | C | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(72): Show |
79 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.121+3985G>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428252 | |||||||
chr22:42428258 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.121+3979C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428258 | |||||||
chr22:42428644 | C | T | 2 | a0001c0001t0009g0074 a0001c0001t0009g0075 |
2 | NA19004.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.121+3593G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428644 | |||||||
chr22:42428657 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.121+3580C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428657 | |||||||
chr22:42428771 | G | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0021 a0001c0001t0017g0019 others(3): Show |
6 | HG02257.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+3466C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428771 | |||||||
chr22:42428795 | C | T | 4 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 others(1): Show |
4 | NA19002.hp2 NA19004.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+3442G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428795 | |||||||
chr22:42428911 | T | G | 1 | a0001c0012t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.121+3326A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428911 | |||||||
chr22:42428942 | G | T | 1 | a0001c0001t0011g0073 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.121+3295C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428942 | |||||||
chr22:42428954 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121+3283C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42428954 | |||||||
chr22:42429022 | G | A | 1 | a0001c0001t0005g0285 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.121+3215C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429022 | |||||||
chr22:42429033 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(99): Show |
106 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.121+3204T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429033 | |||||||
chr22:42429162 | A | G | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121+3075T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429162 | |||||||
chr22:42429276 | C | A | 4 | a0001c0001t0017g0359 a0004c0007t0018g0358 a0004c0007t0018g0360 others(1): Show |
4 | HG00639.hp2 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+2961G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429276 | |||||||
chr22:42429434 | G | A | 10 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(7): Show |
10 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+2803C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429434 | |||||||
chr22:42429530 | C | A | 2 | a0001c0001t0005g0356 a0001c0001t0005g0357 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.121+2707G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429530 | |||||||
chr22:42429547 | C | T | 10 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(7): Show |
10 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+2690G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429547 | |||||||
chr22:42429611 | G | A | 1 | a0001c0001t0010g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.121+2626C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429611 | |||||||
chr22:42429636 | A | T | 58 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0194 others(55): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.121+2601T>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429636 | |||||||
chr22:42429708 | A | G | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121+2529T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429708 | |||||||
chr22:42429932 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0066 others(4): Show |
8 | NA18612.hp2 NA18942.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.121+2305G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429932 | |||||||
chr22:42429950 | T | G | 1 | a0001c0001t0002g0339 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.121+2287A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42429950 | |||||||
chr22:42430000 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.121+2237G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430000 | |||||||
chr22:42430099 | C | A | 9 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(6): Show |
9 | HG00642.hp2 HG01256.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+2138G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430099 | |||||||
chr22:42430099 | C | T | 1 | a0001c0001t0038g0364 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.121+2138G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430099 | |||||||
chr22:42430127 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.121+2110C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430127 | |||||||
chr22:42430294 | T | G | 37 | a0001c0001t0001g0155 a0001c0001t0010g0176 a0001c0001t0050g0156 others(34): Show |
41 | HG00099.hp1 HG00735.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.121+1943A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430294 | |||||||
chr22:42430345 | C | T | 1 | a0001c0001t0026g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+1892G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430345 | |||||||
chr22:42430468 | G | A | 4 | a0001c0001t0017g0359 a0004c0007t0018g0358 a0004c0007t0018g0360 others(1): Show |
4 | HG00639.hp2 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+1769C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430468 | |||||||
chr22:42430485 | A | G | 9 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(6): Show |
9 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+1752T>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430485 | |||||||
chr22:42430556 | C | CA | 106 | a0001c0001t0001g0185 a0001c0001t0001g0193 a0001c0001t0001g0194 others(103): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.121+1680dupT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430556 | |||||||
chr22:42430556 | C | CAA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0304 a0001c0001t0001g0306 others(61): Show |
66 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.121+1679_121+1680d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430556 | |||||||
chr22:42430556 | C | CAAA | 21 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0017g0359 others(18): Show |
23 | HG00438.hp1 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.121+1678_121+1680d others(5): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430556 | |||||||
chr22:42430556 | CA | C | 26 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(23): Show |
26 | HG01168.hp2 HG01516.hp1 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+1680delT | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430556 | |||||||
chr22:42430556 | CAA | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0005g0356 others(3): Show |
7 | HG01433.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+1679_121+1680d others(4): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430556 | |||||||
chr22:42430580 | T | G | 1 | a0001c0001t0005g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.121+1657A>C | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430580 | |||||||
chr22:42430704 | T | C | 1 | a0001c0001t0036g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.121+1533A>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430704 | |||||||
chr22:42430995 | G | C | 8 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0030 others(5): Show |
8 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.121+1242C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42430995 | |||||||
chr22:42431067 | G | A | 3 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0003c0006t0016g0032 |
3 | HG02717.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121+1170C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431067 | |||||||
chr22:42431286 | C | T | 1 | a0001c0001t0009g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.121+951G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431286 | |||||||
chr22:42431749 | G | A | 1 | a0001c0001t0026g0033 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.121+488C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431749 | |||||||
chr22:42431753 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(91): Show |
98 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.121+484T>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431753 | |||||||
chr22:42431775 | T | TC | 72 | a0001c0001t0001g0002 a0001c0001t0001g0295 a0001c0001t0001g0304 others(69): Show |
76 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.121+461dupG | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431775 | |||||||
chr22:42431781 | C | A | 1 | a0001c0003t0007g0355 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121+456G>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431781 | |||||||
chr22:42431782 | CTCCCCCC others(1): Show |
C | 6 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0017g0359 others(3): Show |
6 | HG00639.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+447_121+454del others(8): Show |
NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431782 | |||||||
chr22:42431784 | C | T | 9 | a0001c0001t0003g0007 a0001c0001t0003g0094 a0001c0001t0003g0096 others(6): Show |
10 | HG02027.hp1 NA18747.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+453G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431784 | |||||||
chr22:42431797 | G | C | 6 | a0001c0001t0005g0356 a0001c0001t0005g0357 a0001c0001t0017g0359 others(3): Show |
6 | HG00639.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+440C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431797 | |||||||
chr22:42431831 | G | C | 1 | a0001c0001t0002g0362 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.121+406C>G | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431831 | |||||||
chr22:42431881 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.121+356G>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431881 | |||||||
chr22:42431947 | G | A | 5 | a0001c0001t0038g0364 a0001c0008t0004g0363 a0001c0008t0040g0365 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+290C>T | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42431947 | |||||||
chr22:42432206 | G | T | 1 | a0001c0001t0002g0015 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.121+31C>A | NFAM1 | ENSG00000235568.7 | transcript | ENST00000329021.10 | protein_coding | 1/5 | chr22 | 42432206 |