Item | Value |
---|---|
geneid | 79937 |
ensemblid | ENSG00000106714.18 |
hgncid | 13834 |
symbol | CNTNAP3 |
name | contactin associated protein family member 3 |
refseq_nuc | NM_033655.5 |
refseq_prot | NP_387504.2 |
ensembl_nuc | ENST00000297668.11 |
ensembl_prot | ENSP00000297668.6 |
mane_status | MANE Select |
chr | chr9 |
start | 39064710 |
end | 39288167 |
strand | - |
ver | v1.2 |
region | chr9:39064710-39288167 |
region5000 | chr9:39059710-39293167 |
regionname0 | CNTNAP3_chr9_39064710_39288167 |
regionname5000 | CNTNAP3_chr9_39059710_39293167 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0002 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0003 | 1/0 | 1288 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0004 | 0/1 | 1288 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
c0002 | 0/1 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
c0003 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
c0004 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 9284 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
t0002 | 1/0 | 9284 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
t0003 | 0/0 | 9287 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
t0004 | 0/0 | 9274 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
a0002c0003 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
a0003c0004 | 1/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 | |
a0004c0002 | 0/1 | 3867 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 13153 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0002c0003t0004 | 0/0 | 13140 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0003c0004t0002 | 1/0 | 13150 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
a0004c0002t0001 | 0/1 | 13150 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | copy fasta | chr9 | 39059710 | 39293167 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
a0002c0003t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
a0003c0004t0002g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
a0004c0002t0001g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG02109 | hp1 | a0002 | c0003 | t0004 | g0001 | AFR | ACB | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
homoSapiens_chm13v2 | hp1 | a0004 | c0002 | t0001 | g0003 | REF | REF | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
homoSapiens_grch38 | hp1 | a0003 | c0004 | t0002 | g0004 | REF | REF | CNTNAP3_chr9_39059710_39293167 | CNTNAP3 | chr9 | 39059710 | 39293167 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:39073961 | T | C | 1 | a0001 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3796A>G | p.Ile1266Val | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3899/13150 | 3796/3867 | 1266/1288 | chr9 | 39073961 | ||
chr9:39085811 | T | C | 2 | a0001a0002 | 2 | HG02109.hp1 HG02109.hp2 |
missense_variant | MODERATE | c.3367A>G | p.Thr1123Ala | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/24 | 3470/13150 | 3367/3867 | 1123/1288 | chr9 | 39085811 | ||
chr9:39103746 | C | T | 1 | a0002 | 1 | HG02109.hp1 | missense_variant&splice_region_variant | MODERATE | c.2534G>A | p.Arg845His | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/24 | 2637/13150 | 2534/3867 | 845/1288 | chr9 | 39103746 | ||
chr9:39118199 | C | A | 1 | a0004 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.2141G>T | p.Gly714Val | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/24 | 2244/13150 | 2141/3867 | 714/1288 | chr9 | 39118199 | ||
chr9:39118208 | G | T | 2 | a0001a0004 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2132C>A | p.Ser711Tyr | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/24 | 2235/13150 | 2132/3867 | 711/1288 | chr9 | 39118208 | ||
chr9:39193247 | C | T | 1 | a0001 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.419G>A | p.Ser140Asn | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/24 | 522/13150 | 419/3867 | 140/1288 | chr9 | 39193247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:39085767 | G | A | 2 | a0001c0001a0002c0003 | 2 | HG02109.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.3411C>T | p.Ala1137Ala | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/24 | 3514/13150 | 3411/3867 | 1137/1288 | chr9 | 39085767 | ||
chr9:39102618 | G | A | 2 | a0001c0001a0002c0003 | 2 | HG02109.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.2634C>T | p.His878His | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/24 | 2737/13150 | 2634/3867 | 878/1288 | chr9 | 39102618 | ||
chr9:39109203 | G | A | 1 | a0001c0001 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2322C>T | p.Ser774Ser | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/24 | 2425/13150 | 2322/3867 | 774/1288 | chr9 | 39109203 | ||
chr9:39118111 | C | T | 2 | a0001c0001a0002c0003 | 2 | HG02109.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.2229G>A | p.Arg743Arg | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/24 | 2332/13150 | 2229/3867 | 743/1288 | chr9 | 39118111 | ||
chr9:39118210 | A | G | 2 | a0001c0001a0004c0002 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.2130T>C | p.Thr710Thr | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/24 | 2233/13150 | 2130/3867 | 710/1288 | chr9 | 39118210 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:39064889 | C | T | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9001G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 9001 | chr9 | 39064889 | |||||
chr9:39065050 | G | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8840C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 8840 | chr9 | 39065050 | |||||
chr9:39065217 | T | C | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8673A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 8673 | chr9 | 39065217 | |||||
chr9:39065485 | T | C | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8405A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 8405 | chr9 | 39065485 | |||||
chr9:39065516 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8374G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 8374 | chr9 | 39065516 | |||||
chr9:39066552 | T | C | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7338A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 7338 | chr9 | 39066552 | |||||
chr9:39066916 | T | C | 2 | a0001c0001t0003a0002c0003t0004 | 2 | HG02109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6974A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 6974 | chr9 | 39066916 | |||||
chr9:39067490 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6400G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 6400 | chr9 | 39067490 | |||||
chr9:39067498 | T | C | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6392A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 6392 | chr9 | 39067498 | |||||
chr9:39067863 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6027G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 6027 | chr9 | 39067863 | |||||
chr9:39067973 | A | G | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5917T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5917 | chr9 | 39067973 | |||||
chr9:39068243 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5634_*5646dupTTTT others(9): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5646 | chr9 | 39068243 | |||||
chr9:39068277 | A | G | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5613T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5613 | chr9 | 39068277 | |||||
chr9:39068432 | T | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5458A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5458 | chr9 | 39068432 | |||||
chr9:39068620 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5270G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5270 | chr9 | 39068620 | |||||
chr9:39068764 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5126G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 5126 | chr9 | 39068764 | |||||
chr9:39068906 | G | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4984C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4984 | chr9 | 39068906 | |||||
chr9:39069240 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4650A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4650 | chr9 | 39069240 | |||||
chr9:39069298 | G | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4592C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4592 | chr9 | 39069298 | |||||
chr9:39069474 | A | G | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4416T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4416 | chr9 | 39069474 | |||||
chr9:39069555 | A | G | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4335T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4335 | chr9 | 39069555 | |||||
chr9:39069649 | G | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4241 | chr9 | 39069649 | |||||
chr9:39069835 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4055G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 4055 | chr9 | 39069835 | |||||
chr9:39069940 | C | A | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3950G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3950 | chr9 | 39069940 | |||||
chr9:39070088 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3802A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3802 | chr9 | 39070088 | |||||
chr9:39070169 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3721A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3721 | chr9 | 39070169 | |||||
chr9:39070385 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3505A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3505 | chr9 | 39070385 | |||||
chr9:39070474 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3416A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 3416 | chr9 | 39070474 | |||||
chr9:39071272 | G | C | 2 | a0001c0001t0003a0002c0003t0004 | 2 | HG02109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2618C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 2618 | chr9 | 39071272 | |||||
chr9:39071322 | T | G | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2568A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 2568 | chr9 | 39071322 | |||||
chr9:39071356 | G | A | 1 | a0002c0003t0004 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2534C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 2534 | chr9 | 39071356 | |||||
chr9:39071706 | T | C | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2184A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 2184 | chr9 | 39071706 | |||||
chr9:39072240 | GAATTTCC others(3): Show |
G | 2 | a0001c0001t0003a0002c0003t0004 | 2 | HG02109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1640_*1649delTATG others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 1640 | chr9 | 39072240 | |||||
chr9:39072252 | C | G | 2 | a0001c0001t0003a0002c0003t0004 | 2 | HG02109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1638G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 1638 | chr9 | 39072252 | |||||
chr9:39072460 | C | T | 1 | a0001c0001t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1430G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 1430 | chr9 | 39072460 | |||||
chr9:39072669 | T | C | 2 | a0001c0001t0003a0002c0003t0004 | 2 | HG02109.hp1 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1221A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 24/24 | 1221 | chr9 | 39072669 | |||||
chr9:39288167 | C | T | 1 | a0004c0002t0001 | 1 | homoSapiens_chm13v2.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/24 | 103 | chr9 | 39288167 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:39074386 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-375A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39074386 | ||||||
chr9:39074417 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-406T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39074417 | ||||||
chr9:39074742 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3746-731A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39074742 | ||||||
chr9:39074912 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-901C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39074912 | ||||||
chr9:39075019 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-1008G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39075019 | ||||||
chr9:39076026 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-2015G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076026 | ||||||
chr9:39076074 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3746-2063C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076074 | ||||||
chr9:39076402 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3745+1983G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076402 | ||||||
chr9:39076634 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3745+1751T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076634 | ||||||
chr9:39076690 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3745+1695G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076690 | ||||||
chr9:39076726 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3745+1659A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076726 | ||||||
chr9:39076954 | T | TCAAA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3745+1427_3745+143 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39076954 | ||||||
chr9:39077325 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3745+1060C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39077325 | ||||||
chr9:39077414 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3745+971T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39077414 | ||||||
chr9:39077479 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3745+906G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39077479 | ||||||
chr9:39077559 | AAAACAAA others(9): Show |
A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3745+810_3745+825d others(18): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 23/23 | chr9 | 39077559 | ||||||
chr9:39078963 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3443-43T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39078963 | ||||||
chr9:39078978 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3443-58G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39078978 | ||||||
chr9:39079353 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3443-433C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079353 | ||||||
chr9:39079614 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3443-694T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079614 | ||||||
chr9:39079676 | C | CAT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-757_3443-756i others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079676 | ||||||
chr9:39079677 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-757A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079677 | ||||||
chr9:39079684 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-764G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079684 | ||||||
chr9:39079699 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-779C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079699 | ||||||
chr9:39079738 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-818C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079738 | ||||||
chr9:39079784 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3443-864C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079784 | ||||||
chr9:39079808 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3443-888T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39079808 | ||||||
chr9:39080311 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1391C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080311 | ||||||
chr9:39080505 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1585A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080505 | ||||||
chr9:39080617 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1697T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080617 | ||||||
chr9:39080621 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1701A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080621 | ||||||
chr9:39080722 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1802G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080722 | ||||||
chr9:39080755 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1835T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080755 | ||||||
chr9:39080869 | T | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1949A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080869 | ||||||
chr9:39080916 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-1996G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39080916 | ||||||
chr9:39081030 | G | GAGT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2111_3443-211 others(7): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081030 | ||||||
chr9:39081120 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2200T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081120 | ||||||
chr9:39081197 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2277T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081197 | ||||||
chr9:39081438 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3443-2518T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081438 | ||||||
chr9:39081483 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2563G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081483 | ||||||
chr9:39081489 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2569G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081489 | ||||||
chr9:39081588 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2668G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081588 | ||||||
chr9:39081848 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2928C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081848 | ||||||
chr9:39081849 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2929A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081849 | ||||||
chr9:39081853 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2933G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081853 | ||||||
chr9:39081863 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2943C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081863 | ||||||
chr9:39081894 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2974G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081894 | ||||||
chr9:39081906 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2986T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081906 | ||||||
chr9:39081914 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-2994A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081914 | ||||||
chr9:39081943 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3443-3023G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081943 | ||||||
chr9:39081953 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3443-3033C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39081953 | ||||||
chr9:39082076 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-3156T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082076 | ||||||
chr9:39082099 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-3179G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082099 | ||||||
chr9:39082201 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-3281T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082201 | ||||||
chr9:39082203 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-3283A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082203 | ||||||
chr9:39082305 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3443-3385A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082305 | ||||||
chr9:39082461 | G | GA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+3274dupT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082461 | ||||||
chr9:39082700 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+3036G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082700 | ||||||
chr9:39082860 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2876G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082860 | ||||||
chr9:39082885 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2851C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39082885 | ||||||
chr9:39083060 | TA | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2675delT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083060 | ||||||
chr9:39083134 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2602A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083134 | ||||||
chr9:39083501 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2235G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083501 | ||||||
chr9:39083531 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+2205A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083531 | ||||||
chr9:39083793 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+1943G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083793 | ||||||
chr9:39083837 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+1899A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083837 | ||||||
chr9:39083998 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+1738T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39083998 | ||||||
chr9:39084278 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+1458G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084278 | ||||||
chr9:39084337 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+1399G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084337 | ||||||
chr9:39084385 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+1351C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084385 | ||||||
chr9:39084474 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3442+1262C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084474 | ||||||
chr9:39084743 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3442+993T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084743 | ||||||
chr9:39084854 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+882T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084854 | ||||||
chr9:39084976 | G | GT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+759dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39084976 | ||||||
chr9:39085043 | TTAAAG | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+688_3442+692d others(7): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085043 | ||||||
chr9:39085085 | GTTT | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+648_3442+650d others(5): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085085 | ||||||
chr9:39085156 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+580T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085156 | ||||||
chr9:39085204 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+532C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085204 | ||||||
chr9:39085208 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+528G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085208 | ||||||
chr9:39085466 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+270T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085466 | ||||||
chr9:39085480 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+256C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085480 | ||||||
chr9:39085561 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+175A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085561 | ||||||
chr9:39085566 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3442+170G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085566 | ||||||
chr9:39085570 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+166C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085570 | ||||||
chr9:39085706 | A | AGATTT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3442+29_3442+30ins others(5): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 21/23 | chr9 | 39085706 | ||||||
chr9:39086245 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3355-422A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086245 | ||||||
chr9:39086375 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3354+341C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086375 | ||||||
chr9:39086452 | T | TAA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3354+263_3354+264i others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086452 | ||||||
chr9:39086634 | A | ATATT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3354+78_3354+81dup others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086634 | ||||||
chr9:39086690 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3354+26A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086690 | ||||||
chr9:39086698 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3354+18A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 20/23 | chr9 | 39086698 | ||||||
chr9:39086943 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3221-94G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39086943 | ||||||
chr9:39087060 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3221-211C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087060 | ||||||
chr9:39087272 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3221-423G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087272 | ||||||
chr9:39087489 | T | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3221-640A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087489 | ||||||
chr9:39087501 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3221-652C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087501 | ||||||
chr9:39087732 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+691A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087732 | ||||||
chr9:39087737 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3220+686A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087737 | ||||||
chr9:39087778 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+645T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087778 | ||||||
chr9:39087788 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+635G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087788 | ||||||
chr9:39087860 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3220+563A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087860 | ||||||
chr9:39087877 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+546T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087877 | ||||||
chr9:39087916 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+507A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39087916 | ||||||
chr9:39088266 | AC | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3220+156delG | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 19/23 | chr9 | 39088266 | ||||||
chr9:39088728 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-81T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39088728 | ||||||
chr9:39088862 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-215T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39088862 | ||||||
chr9:39088865 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2996-218A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39088865 | ||||||
chr9:39089188 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-541T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39089188 | ||||||
chr9:39089261 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-614G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39089261 | ||||||
chr9:39089387 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-740A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39089387 | ||||||
chr9:39089393 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-746C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39089393 | ||||||
chr9:39090113 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2996-1466C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090113 | ||||||
chr9:39090310 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-1663G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090310 | ||||||
chr9:39090376 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-1729C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090376 | ||||||
chr9:39090387 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-1740C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090387 | ||||||
chr9:39090523 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-1876A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090523 | ||||||
chr9:39090556 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-1909A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090556 | ||||||
chr9:39090746 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-2099T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090746 | ||||||
chr9:39090908 | A | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-2261T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090908 | ||||||
chr9:39090964 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-2317G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39090964 | ||||||
chr9:39091171 | C | CT | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2996-2525dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39091171 | ||||||
chr9:39091968 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-3321A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39091968 | ||||||
chr9:39092368 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-3721C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092368 | ||||||
chr9:39092439 | A | ATGT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-3795_2996-379 others(7): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092439 | ||||||
chr9:39092545 | TTA | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-3900_2996-389 others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092545 | ||||||
chr9:39092556 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-3909A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092556 | ||||||
chr9:39092785 | T | TTATTC | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4139_2996-413 others(9): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092785 | ||||||
chr9:39092798 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4151A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092798 | ||||||
chr9:39092938 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4291C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092938 | ||||||
chr9:39092956 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2996-4309A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092956 | ||||||
chr9:39092969 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4322C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39092969 | ||||||
chr9:39093183 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2996-4536C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093183 | ||||||
chr9:39093194 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4547C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093194 | ||||||
chr9:39093202 | TTTAATA | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4561_2996-455 others(10): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093202 | ||||||
chr9:39093394 | TG | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4748delC | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093394 | ||||||
chr9:39093429 | C | CATTA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4786_2996-478 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093429 | ||||||
chr9:39093572 | C | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-4925G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093572 | ||||||
chr9:39093705 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2996-5058G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093705 | ||||||
chr9:39093921 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-5274G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39093921 | ||||||
chr9:39094035 | TTTTA | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2996-5392_2996-538 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39094035 | ||||||
chr9:39094505 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+5406T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39094505 | ||||||
chr9:39094572 | CT | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+5338delA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39094572 | ||||||
chr9:39094928 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4983A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39094928 | ||||||
chr9:39094987 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4924A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39094987 | ||||||
chr9:39095041 | GTCTT | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4866_2995+486 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095041 | ||||||
chr9:39095441 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4470T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095441 | ||||||
chr9:39095461 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4450C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095461 | ||||||
chr9:39095476 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4435C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095476 | ||||||
chr9:39095496 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2995+4415G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095496 | ||||||
chr9:39095564 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+4347G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095564 | ||||||
chr9:39095617 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4294C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095617 | ||||||
chr9:39095682 | C | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4229G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095682 | ||||||
chr9:39095698 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4213A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095698 | ||||||
chr9:39095710 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4201A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095710 | ||||||
chr9:39095795 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+4116A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095795 | ||||||
chr9:39095966 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3945A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39095966 | ||||||
chr9:39096009 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3902A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096009 | ||||||
chr9:39096070 | CTCCTCTG others(218): Show |
C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3616_2995+384 others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096070 | ||||||
chr9:39096362 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3549C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096362 | ||||||
chr9:39096372 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3539A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096372 | ||||||
chr9:39096525 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3386G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096525 | ||||||
chr9:39096579 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3332C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096579 | ||||||
chr9:39096631 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+3280G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096631 | ||||||
chr9:39096645 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3266G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096645 | ||||||
chr9:39096679 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3232T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096679 | ||||||
chr9:39096714 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3197A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096714 | ||||||
chr9:39096890 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+3021A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096890 | ||||||
chr9:39096929 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2982C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096929 | ||||||
chr9:39096985 | GTATTTTC others(9): Show |
G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2910_2995+292 others(20): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39096985 | ||||||
chr9:39097182 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2729T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097182 | ||||||
chr9:39097322 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2589C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097322 | ||||||
chr9:39097402 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+2509C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097402 | ||||||
chr9:39097523 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2388G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097523 | ||||||
chr9:39097694 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2217G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097694 | ||||||
chr9:39097761 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2150A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097761 | ||||||
chr9:39097852 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+2059G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39097852 | ||||||
chr9:39098017 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1894A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098017 | ||||||
chr9:39098076 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+1835G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098076 | ||||||
chr9:39098151 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1760C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098151 | ||||||
chr9:39098213 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1698T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098213 | ||||||
chr9:39098255 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1656T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098255 | ||||||
chr9:39098308 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+1603G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098308 | ||||||
chr9:39098336 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1575G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098336 | ||||||
chr9:39098701 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+1210C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39098701 | ||||||
chr9:39099535 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2995+376C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39099535 | ||||||
chr9:39099613 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2995+298T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 18/23 | chr9 | 39099613 | ||||||
chr9:39100341 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2756-191G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39100341 | ||||||
chr9:39100480 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2756-330G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39100480 | ||||||
chr9:39100609 | T | TA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2756-460dupT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39100609 | ||||||
chr9:39100691 | A | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2756-541T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39100691 | ||||||
chr9:39101043 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2756-893G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101043 | ||||||
chr9:39101113 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2756-963A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101113 | ||||||
chr9:39101261 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2756-1111T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101261 | ||||||
chr9:39101327 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2755+1170C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101327 | ||||||
chr9:39101461 | T | TAGCAAAA others(16): Show |
2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+1035_2755+103 others(27): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101461 | ||||||
chr9:39101569 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+928T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101569 | ||||||
chr9:39101845 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+652C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101845 | ||||||
chr9:39101924 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+573A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39101924 | ||||||
chr9:39102061 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+436A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39102061 | ||||||
chr9:39102077 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2755+420G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39102077 | ||||||
chr9:39102205 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2755+292C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39102205 | ||||||
chr9:39102254 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2755+243A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 17/23 | chr9 | 39102254 | ||||||
chr9:39102897 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2537-182C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39102897 | ||||||
chr9:39102998 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2537-283A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39102998 | ||||||
chr9:39103056 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2537-341G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39103056 | ||||||
chr9:39103268 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2536+476G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39103268 | ||||||
chr9:39103303 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2536+441A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39103303 | ||||||
chr9:39103347 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2536+397G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39103347 | ||||||
chr9:39103386 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2536+358T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 16/23 | chr9 | 39103386 | ||||||
chr9:39104339 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-425G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39104339 | ||||||
chr9:39104477 | T | TAC | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2366-565_2366-564d others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39104477 | ||||||
chr9:39104477 | T | TACACATA others(3): Show |
1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-564_2366-563i others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39104477 | ||||||
chr9:39104550 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-636T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39104550 | ||||||
chr9:39105382 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-1468T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39105382 | ||||||
chr9:39105440 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2366-1526G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39105440 | ||||||
chr9:39108524 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2365+636G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 15/23 | chr9 | 39108524 | ||||||
chr9:39110268 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2238-981G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39110268 | ||||||
chr9:39112045 | T | TTCTC | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2238-2759_2238-275 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39112045 | ||||||
chr9:39112967 | T | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2238-3680A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39112967 | ||||||
chr9:39114023 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+4080A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114023 | ||||||
chr9:39114029 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+4074G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114029 | ||||||
chr9:39114033 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+4070A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114033 | ||||||
chr9:39114035 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+4068A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114035 | ||||||
chr9:39114055 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+4048G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114055 | ||||||
chr9:39114057 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2237+4046A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114057 | ||||||
chr9:39114069 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2237+4034G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114069 | ||||||
chr9:39114079 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2237+4024A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39114079 | ||||||
chr9:39116585 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2237+1518C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39116585 | ||||||
chr9:39116719 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+1384C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39116719 | ||||||
chr9:39117970 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2237+133T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 14/23 | chr9 | 39117970 | ||||||
chr9:39118937 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-678G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39118937 | ||||||
chr9:39119176 | G | C | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2081-917C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39119176 | ||||||
chr9:39119176 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-917C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39119176 | ||||||
chr9:39120385 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2081-2126G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39120385 | ||||||
chr9:39120507 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-2248A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39120507 | ||||||
chr9:39120737 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2081-2478C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39120737 | ||||||
chr9:39121444 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2081-3185C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39121444 | ||||||
chr9:39121526 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-3267G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39121526 | ||||||
chr9:39122121 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-3862C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39122121 | ||||||
chr9:39122597 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2081-4338C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39122597 | ||||||
chr9:39122890 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-4631A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39122890 | ||||||
chr9:39123012 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-4753G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123012 | ||||||
chr9:39123059 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-4800T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123059 | ||||||
chr9:39123091 | AT | A | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2081-4833delA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123091 | ||||||
chr9:39123447 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-5188G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123447 | ||||||
chr9:39123672 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-5413G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123672 | ||||||
chr9:39123815 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-5556T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39123815 | ||||||
chr9:39124722 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2081-6463C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39124722 | ||||||
chr9:39125626 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+7306T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39125626 | ||||||
chr9:39125759 | G | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+7173C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39125759 | ||||||
chr9:39126277 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+6655T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39126277 | ||||||
chr9:39126691 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+6241G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39126691 | ||||||
chr9:39126712 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+6220G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39126712 | ||||||
chr9:39128225 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+4707A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39128225 | ||||||
chr9:39128726 | C | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+4206G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39128726 | ||||||
chr9:39128880 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+4052C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39128880 | ||||||
chr9:39129186 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+3746T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39129186 | ||||||
chr9:39130098 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+2834T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39130098 | ||||||
chr9:39130597 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2080+2335A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39130597 | ||||||
chr9:39130706 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2080+2226T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39130706 | ||||||
chr9:39131292 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+1640T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39131292 | ||||||
chr9:39131871 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2080+1061T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39131871 | ||||||
chr9:39131903 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+1029G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39131903 | ||||||
chr9:39131976 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+956T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39131976 | ||||||
chr9:39132001 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2080+931G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39132001 | ||||||
chr9:39132129 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+803A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39132129 | ||||||
chr9:39132250 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2080+682T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39132250 | ||||||
chr9:39132602 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+330A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39132602 | ||||||
chr9:39132743 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080+189G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 13/23 | chr9 | 39132743 | ||||||
chr9:39133171 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1877-36T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39133171 | ||||||
chr9:39133494 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1877-359A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39133494 | ||||||
chr9:39135025 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1877-1890G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39135025 | ||||||
chr9:39135286 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1877-2151A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39135286 | ||||||
chr9:39135427 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1877-2292T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39135427 | ||||||
chr9:39135447 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1877-2312A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39135447 | ||||||
chr9:39137187 | T | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+3332A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39137187 | ||||||
chr9:39137377 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+3142A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39137377 | ||||||
chr9:39138073 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+2446A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138073 | ||||||
chr9:39138403 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+2116G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138403 | ||||||
chr9:39138480 | G | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+2039C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138480 | ||||||
chr9:39138554 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+1965G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138554 | ||||||
chr9:39138570 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1876+1949A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138570 | ||||||
chr9:39138734 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1876+1785T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39138734 | ||||||
chr9:39139786 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1876+733A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39139786 | ||||||
chr9:39139876 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1876+643G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39139876 | ||||||
chr9:39140230 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1876+289A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 12/23 | chr9 | 39140230 | ||||||
chr9:39140803 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1757-165A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39140803 | ||||||
chr9:39141078 | C | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1757-440G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39141078 | ||||||
chr9:39141161 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1757-523T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39141161 | ||||||
chr9:39142014 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1757-1376T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39142014 | ||||||
chr9:39142276 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1757-1638C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39142276 | ||||||
chr9:39142564 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1756+1676G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39142564 | ||||||
chr9:39142650 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1756+1590G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39142650 | ||||||
chr9:39142752 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1756+1488T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39142752 | ||||||
chr9:39143169 | T | TCA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1756+1069_1756+107 others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39143169 | ||||||
chr9:39143217 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1756+1023C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39143217 | ||||||
chr9:39143218 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1756+1022C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39143218 | ||||||
chr9:39143330 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1756+910G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 11/23 | chr9 | 39143330 | ||||||
chr9:39144860 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1650-514G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39144860 | ||||||
chr9:39145021 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1650-675A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145021 | ||||||
chr9:39145457 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1111G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145457 | ||||||
chr9:39145558 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1650-1212C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145558 | ||||||
chr9:39145565 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1650-1219C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145565 | ||||||
chr9:39145670 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1324G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145670 | ||||||
chr9:39145696 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1350C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145696 | ||||||
chr9:39145755 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1409G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145755 | ||||||
chr9:39145817 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1471G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145817 | ||||||
chr9:39145826 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1480A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145826 | ||||||
chr9:39145905 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1559G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145905 | ||||||
chr9:39145905 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1650-1559G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145905 | ||||||
chr9:39145913 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1650-1567A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39145913 | ||||||
chr9:39146013 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1650-1667T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39146013 | ||||||
chr9:39146034 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1650-1688G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39146034 | ||||||
chr9:39146127 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1781C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39146127 | ||||||
chr9:39146293 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-1947C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39146293 | ||||||
chr9:39146411 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-2065G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39146411 | ||||||
chr9:39147048 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1650-2702C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147048 | ||||||
chr9:39147108 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1649+2698C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147108 | ||||||
chr9:39147266 | T | TTTTG | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1649+2536_1649+253 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147266 | ||||||
chr9:39147535 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+2271C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147535 | ||||||
chr9:39147697 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1649+2109G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147697 | ||||||
chr9:39147718 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1649+2088A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39147718 | ||||||
chr9:39148165 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1649+1641T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39148165 | ||||||
chr9:39148526 | CT | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1649+1279delA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39148526 | ||||||
chr9:39148761 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+1045T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39148761 | ||||||
chr9:39148772 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+1034A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39148772 | ||||||
chr9:39148820 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1649+986C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39148820 | ||||||
chr9:39149212 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1649+594C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39149212 | ||||||
chr9:39149372 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1649+434G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39149372 | ||||||
chr9:39149532 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1649+274T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39149532 | ||||||
chr9:39149602 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1649+204T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 10/23 | chr9 | 39149602 | ||||||
chr9:39150261 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-284C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39150261 | ||||||
chr9:39150994 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-1017G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39150994 | ||||||
chr9:39151008 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-1031C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39151008 | ||||||
chr9:39151339 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-1362G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39151339 | ||||||
chr9:39151566 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-1589T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39151566 | ||||||
chr9:39151739 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-1762G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39151739 | ||||||
chr9:39151839 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-1862G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39151839 | ||||||
chr9:39152018 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1478-2041G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39152018 | ||||||
chr9:39152162 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-2185T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39152162 | ||||||
chr9:39152694 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-2717G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39152694 | ||||||
chr9:39153035 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1478-3058T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39153035 | ||||||
chr9:39153661 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-3684G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39153661 | ||||||
chr9:39153904 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-3927A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39153904 | ||||||
chr9:39154602 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-4625A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39154602 | ||||||
chr9:39154810 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1478-4833G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39154810 | ||||||
chr9:39155011 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1478-5034A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39155011 | ||||||
chr9:39156173 | C | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1478-6196G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39156173 | ||||||
chr9:39156278 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-6301C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39156278 | ||||||
chr9:39156673 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-6696A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39156673 | ||||||
chr9:39157558 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-7581G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39157558 | ||||||
chr9:39157574 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1478-7597A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39157574 | ||||||
chr9:39158145 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7788G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39158145 | ||||||
chr9:39158214 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7719T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39158214 | ||||||
chr9:39158239 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7694C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39158239 | ||||||
chr9:39158334 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1477+7599G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39158334 | ||||||
chr9:39158455 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+7478T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39158455 | ||||||
chr9:39159097 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1477+6836C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159097 | ||||||
chr9:39159330 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6603G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159330 | ||||||
chr9:39159479 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6454A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159479 | ||||||
chr9:39159512 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6421A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159512 | ||||||
chr9:39159633 | TAGATAGA others(7): Show |
T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6286_1477+629 others(18): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159633 | ||||||
chr9:39159651 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6282C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159651 | ||||||
chr9:39159655 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6278C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159655 | ||||||
chr9:39159663 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6270C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159663 | ||||||
chr9:39159667 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6266C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159667 | ||||||
chr9:39159671 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6262C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159671 | ||||||
chr9:39159907 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+6026G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39159907 | ||||||
chr9:39162015 | A | AG | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1477+3917dupC | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39162015 | ||||||
chr9:39162151 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+3782C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39162151 | ||||||
chr9:39163460 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+2473T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39163460 | ||||||
chr9:39163556 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+2377C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39163556 | ||||||
chr9:39163812 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1477+2121C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39163812 | ||||||
chr9:39164646 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+1287C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39164646 | ||||||
chr9:39164748 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1477+1185T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 9/23 | chr9 | 39164748 | ||||||
chr9:39167027 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-951T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39167027 | ||||||
chr9:39167221 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-1145T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39167221 | ||||||
chr9:39167597 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-1521T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39167597 | ||||||
chr9:39168006 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1334-1930C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39168006 | ||||||
chr9:39168016 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-1940C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39168016 | ||||||
chr9:39168022 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1334-1946C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39168022 | ||||||
chr9:39169030 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+2339T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39169030 | ||||||
chr9:39169081 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+2288C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39169081 | ||||||
chr9:39169176 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+2193G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39169176 | ||||||
chr9:39169424 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+1945C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39169424 | ||||||
chr9:39169730 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+1639G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39169730 | ||||||
chr9:39170185 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+1184A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39170185 | ||||||
chr9:39170999 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1333+370C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 8/23 | chr9 | 39170999 | ||||||
chr9:39173092 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072-1462G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39173092 | ||||||
chr9:39173193 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1072-1563C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39173193 | ||||||
chr9:39173316 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1072-1686T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39173316 | ||||||
chr9:39173586 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1072-1956A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39173586 | ||||||
chr9:39173927 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+2022A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39173927 | ||||||
chr9:39174028 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+1921C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39174028 | ||||||
chr9:39174793 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+1156C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39174793 | ||||||
chr9:39175011 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+938G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39175011 | ||||||
chr9:39175135 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1071+814C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39175135 | ||||||
chr9:39175265 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+684C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39175265 | ||||||
chr9:39175370 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+579T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39175370 | ||||||
chr9:39175391 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1071+558C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 7/23 | chr9 | 39175391 | ||||||
chr9:39177641 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.743-139G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 5/23 | chr9 | 39177641 | ||||||
chr9:39177736 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.743-234T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 5/23 | chr9 | 39177736 | ||||||
chr9:39177833 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.742+324A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 5/23 | chr9 | 39177833 | ||||||
chr9:39177949 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.742+208A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 5/23 | chr9 | 39177949 | ||||||
chr9:39178379 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-19C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39178379 | ||||||
chr9:39178417 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-57G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39178417 | ||||||
chr9:39178560 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-200C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39178560 | ||||||
chr9:39178562 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-202T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39178562 | ||||||
chr9:39179286 | T | TACACACA others(5): Show |
1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.539-938_539-927dup others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179286 | ||||||
chr9:39179286 | TACACACA others(4): Show |
T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-937_539-927del others(11): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179286 | ||||||
chr9:39179286 | TACACACA others(5): Show |
T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.539-938_539-927del others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179286 | ||||||
chr9:39179299 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-939T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179299 | ||||||
chr9:39179302 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-942G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179302 | ||||||
chr9:39179492 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-1132A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39179492 | ||||||
chr9:39180163 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-1803A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39180163 | ||||||
chr9:39181117 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-2757A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39181117 | ||||||
chr9:39181123 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-2763T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39181123 | ||||||
chr9:39181516 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.539-3156G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39181516 | ||||||
chr9:39181838 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.539-3478G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39181838 | ||||||
chr9:39181958 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-3598C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39181958 | ||||||
chr9:39182027 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.539-3667A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39182027 | ||||||
chr9:39182157 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-3797A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39182157 | ||||||
chr9:39182455 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-4095T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39182455 | ||||||
chr9:39182477 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-4117G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39182477 | ||||||
chr9:39182492 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-4132G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39182492 | ||||||
chr9:39183456 | G | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.539-5096C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39183456 | ||||||
chr9:39183686 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-5326G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39183686 | ||||||
chr9:39184068 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.539-5708T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184068 | ||||||
chr9:39184217 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-5857G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184217 | ||||||
chr9:39184386 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6026T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184386 | ||||||
chr9:39184893 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6533T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184893 | ||||||
chr9:39184894 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6534C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184894 | ||||||
chr9:39184946 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6586C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184946 | ||||||
chr9:39184952 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6592A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39184952 | ||||||
chr9:39185024 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6664A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39185024 | ||||||
chr9:39185033 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6673C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39185033 | ||||||
chr9:39185070 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.539-6710G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39185070 | ||||||
chr9:39185139 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-6779C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39185139 | ||||||
chr9:39186437 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+6691G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39186437 | ||||||
chr9:39186507 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+6621T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39186507 | ||||||
chr9:39186596 | T | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+6532A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39186596 | ||||||
chr9:39186634 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+6494A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39186634 | ||||||
chr9:39188600 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+4528C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39188600 | ||||||
chr9:39188650 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+4478G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39188650 | ||||||
chr9:39188950 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+4178C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39188950 | ||||||
chr9:39189598 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+3530G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39189598 | ||||||
chr9:39189703 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+3425C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39189703 | ||||||
chr9:39189774 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+3354C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39189774 | ||||||
chr9:39189779 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+3349G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39189779 | ||||||
chr9:39190120 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+3008C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190120 | ||||||
chr9:39190216 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+2912G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190216 | ||||||
chr9:39190274 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+2854C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190274 | ||||||
chr9:39190336 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+2792G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190336 | ||||||
chr9:39190354 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+2774G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190354 | ||||||
chr9:39190423 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+2705G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39190423 | ||||||
chr9:39191089 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.538+2039C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39191089 | ||||||
chr9:39191438 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+1690C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39191438 | ||||||
chr9:39191766 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+1362A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39191766 | ||||||
chr9:39192791 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.538+337T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 4/23 | chr9 | 39192791 | ||||||
chr9:39194435 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-1160G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39194435 | ||||||
chr9:39194542 | CAA | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-1269_391-1268d others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39194542 | ||||||
chr9:39194781 | C | CTTTTTTT others(3): Show |
1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-1516_391-1507d others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39194781 | ||||||
chr9:39194781 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-1518_391-1507d others(14): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39194781 | ||||||
chr9:39195534 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-2259A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39195534 | ||||||
chr9:39196054 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-2779A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39196054 | ||||||
chr9:39196169 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-2894G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39196169 | ||||||
chr9:39196380 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-3105A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39196380 | ||||||
chr9:39197606 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-4331T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39197606 | ||||||
chr9:39197671 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-4396G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39197671 | ||||||
chr9:39198036 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-4761C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39198036 | ||||||
chr9:39198083 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-4808G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39198083 | ||||||
chr9:39198218 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-4943A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39198218 | ||||||
chr9:39198727 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-5452T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39198727 | ||||||
chr9:39200260 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-6985G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39200260 | ||||||
chr9:39200352 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-7077G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39200352 | ||||||
chr9:39200511 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-7236C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39200511 | ||||||
chr9:39201454 | C | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-8179G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39201454 | ||||||
chr9:39201719 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-8444T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39201719 | ||||||
chr9:39201869 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-8594G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39201869 | ||||||
chr9:39202109 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-8834G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202109 | ||||||
chr9:39202308 | T | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-9033A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202308 | ||||||
chr9:39202339 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-9064G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202339 | ||||||
chr9:39202355 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9080T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202355 | ||||||
chr9:39202588 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-9313T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202588 | ||||||
chr9:39202677 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9402G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202677 | ||||||
chr9:39202966 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9691C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202966 | ||||||
chr9:39202972 | G | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-9697C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39202972 | ||||||
chr9:39203011 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-9736C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39203011 | ||||||
chr9:39203164 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-9889T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39203164 | ||||||
chr9:39203773 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-10498C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39203773 | ||||||
chr9:39203961 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-10686G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39203961 | ||||||
chr9:39204043 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-10768C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39204043 | ||||||
chr9:39204852 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-11577C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39204852 | ||||||
chr9:39204967 | AATCATCA others(8): Show |
A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-11707_391-1169 others(19): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39204967 | ||||||
chr9:39205083 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-11808A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205083 | ||||||
chr9:39205169 | CT | C | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-11895delA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205169 | ||||||
chr9:39205428 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-12153C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205428 | ||||||
chr9:39205462 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-12187T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205462 | ||||||
chr9:39205755 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-12480T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205755 | ||||||
chr9:39205853 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-12578A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205853 | ||||||
chr9:39205881 | A | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-12606T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39205881 | ||||||
chr9:39206544 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-13269C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39206544 | ||||||
chr9:39206588 | CAG | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-13315_391-1331 others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39206588 | ||||||
chr9:39207596 | A | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-14321T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39207596 | ||||||
chr9:39208335 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15060A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39208335 | ||||||
chr9:39208373 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15098T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39208373 | ||||||
chr9:39208543 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15268G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39208543 | ||||||
chr9:39208744 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-15469A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39208744 | ||||||
chr9:39208822 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15547G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39208822 | ||||||
chr9:39209181 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-15906G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209181 | ||||||
chr9:39209215 | T | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-15940A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209215 | ||||||
chr9:39209337 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-16062G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209337 | ||||||
chr9:39209442 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-16167T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209442 | ||||||
chr9:39209599 | TTCCC | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-16328_391-1632 others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209599 | ||||||
chr9:39209690 | CCCTTCCT others(1): Show |
C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-16423_391-1641 others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209690 | ||||||
chr9:39209702 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-16427A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209702 | ||||||
chr9:39209747 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-16472C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209747 | ||||||
chr9:39209791 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-16516T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39209791 | ||||||
chr9:39210129 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-16854C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39210129 | ||||||
chr9:39210356 | G | A | 2 | a0001c0001t0003g0002a0004c0002t0001g0003 | 2 | HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-17081C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39210356 | ||||||
chr9:39210579 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-17304A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39210579 | ||||||
chr9:39211081 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-17806A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211081 | ||||||
chr9:39211103 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-17828A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211103 | ||||||
chr9:39211398 | T | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-18123A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211398 | ||||||
chr9:39211717 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-18442C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211717 | ||||||
chr9:39211863 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-18588A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211863 | ||||||
chr9:39211990 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-18715G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39211990 | ||||||
chr9:39212017 | CACT | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-18745_391-1874 others(7): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212017 | ||||||
chr9:39212104 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-18829C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212104 | ||||||
chr9:39212165 | A | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-18890T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212165 | ||||||
chr9:39212453 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-19178C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212453 | ||||||
chr9:39212713 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-19438G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212713 | ||||||
chr9:39212879 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-19604T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212879 | ||||||
chr9:39212909 | A | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-19634T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212909 | ||||||
chr9:39212949 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-19674C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39212949 | ||||||
chr9:39213186 | GAGAGGAG others(8): Show |
G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-19926_391-1991 others(19): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213186 | ||||||
chr9:39213191 | GAGAGAAG others(3): Show |
G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-19926_391-1991 others(14): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213191 | ||||||
chr9:39213191 | GAGAGAAG others(13): Show |
G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-19936_391-1991 others(24): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213191 | ||||||
chr9:39213293 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-20018A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213293 | ||||||
chr9:39213447 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-20172G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213447 | ||||||
chr9:39213689 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-20414C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213689 | ||||||
chr9:39213967 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-20692T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213967 | ||||||
chr9:39213998 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-20723A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39213998 | ||||||
chr9:39214544 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-21269A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39214544 | ||||||
chr9:39214695 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-21420C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39214695 | ||||||
chr9:39214891 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-21616A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39214891 | ||||||
chr9:39214979 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-21704C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39214979 | ||||||
chr9:39215213 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-21938G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39215213 | ||||||
chr9:39215220 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.391-21945A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39215220 | ||||||
chr9:39215581 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.391-22306T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39215581 | ||||||
chr9:39215924 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.391-22649A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39215924 | ||||||
chr9:39216582 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+22411C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39216582 | ||||||
chr9:39216822 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+22171G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39216822 | ||||||
chr9:39217270 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+21723G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217270 | ||||||
chr9:39217358 | GTATATAT others(17): Show |
G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+21611_390+2163 others(28): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217358 | ||||||
chr9:39217358 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+21609_390+2163 others(30): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217358 | ||||||
chr9:39217537 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+21456C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217537 | ||||||
chr9:39217673 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+21320A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217673 | ||||||
chr9:39217727 | A | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+21266T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217727 | ||||||
chr9:39217869 | A | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+21124T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39217869 | ||||||
chr9:39218078 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+20915T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218078 | ||||||
chr9:39218132 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+20861A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218132 | ||||||
chr9:39218151 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+20842T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218151 | ||||||
chr9:39218471 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+20522C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218471 | ||||||
chr9:39218577 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+20416T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218577 | ||||||
chr9:39218599 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+20394A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218599 | ||||||
chr9:39218672 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+20321T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218672 | ||||||
chr9:39218810 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+20183A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218810 | ||||||
chr9:39218854 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+20139T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218854 | ||||||
chr9:39218933 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+20060G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39218933 | ||||||
chr9:39219011 | C | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19982G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219011 | ||||||
chr9:39219284 | C | CT | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+19708dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219284 | ||||||
chr9:39219284 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19709G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219284 | ||||||
chr9:39219306 | C | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+19687G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219306 | ||||||
chr9:39219365 | A | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19628T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219365 | ||||||
chr9:39219408 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19585G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219408 | ||||||
chr9:39219433 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+19560C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39219433 | ||||||
chr9:39220400 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+18593T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39220400 | ||||||
chr9:39220438 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+18555A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39220438 | ||||||
chr9:39220898 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+18095C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39220898 | ||||||
chr9:39221109 | C | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+17884G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39221109 | ||||||
chr9:39221144 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+17849G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39221144 | ||||||
chr9:39221190 | G | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+17803C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39221190 | ||||||
chr9:39221602 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+17391A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39221602 | ||||||
chr9:39221639 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+17354T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39221639 | ||||||
chr9:39222018 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+16975C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222018 | ||||||
chr9:39222319 | A | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+16674T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222319 | ||||||
chr9:39222341 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+16652A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222341 | ||||||
chr9:39222361 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+16632G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222361 | ||||||
chr9:39222547 | G | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+16446C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222547 | ||||||
chr9:39222697 | A | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+16296T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222697 | ||||||
chr9:39222726 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+16267C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39222726 | ||||||
chr9:39223156 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+15837A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39223156 | ||||||
chr9:39224110 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14883A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39224110 | ||||||
chr9:39224136 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14857A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39224136 | ||||||
chr9:39224140 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14853A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39224140 | ||||||
chr9:39224250 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+14743G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39224250 | ||||||
chr9:39225243 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+13750A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39225243 | ||||||
chr9:39225829 | T | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390+13164A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39225829 | ||||||
chr9:39226934 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+12059T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226934 | ||||||
chr9:39226936 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+12057C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226936 | ||||||
chr9:39226938 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+12055C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226938 | ||||||
chr9:39226940 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+12053C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226940 | ||||||
chr9:39226951 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+12042A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226951 | ||||||
chr9:39226951 | T | TATATATA others(19): Show |
1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+12041_390+1204 others(30): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39226951 | ||||||
chr9:39227933 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+11060T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39227933 | ||||||
chr9:39228043 | T | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+10950A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39228043 | ||||||
chr9:39228544 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+10439_390+1044 others(14): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39228544 | ||||||
chr9:39229118 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+9875C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39229118 | ||||||
chr9:39229446 | TAC | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+9545_390+9546d others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39229446 | ||||||
chr9:39229786 | C | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+9207G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39229786 | ||||||
chr9:39229793 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+9200T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39229793 | ||||||
chr9:39230172 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+8821T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39230172 | ||||||
chr9:39230832 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+8161G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39230832 | ||||||
chr9:39231103 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+7890G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231103 | ||||||
chr9:39231574 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+7419G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231574 | ||||||
chr9:39231827 | G | GTTC | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+7163_390+7165d others(5): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231827 | ||||||
chr9:39231948 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+7045T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231948 | ||||||
chr9:39231954 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+7039C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231954 | ||||||
chr9:39231954 | G | GTGTGTGT others(13): Show |
2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+7038_390+7039i others(22): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231954 | ||||||
chr9:39231973 | A | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+7020T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231973 | ||||||
chr9:39231977 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+7016C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39231977 | ||||||
chr9:39232866 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+6127C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39232866 | ||||||
chr9:39232896 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+6097C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39232896 | ||||||
chr9:39233006 | T | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+5987A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39233006 | ||||||
chr9:39233028 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+5965C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39233028 | ||||||
chr9:39233667 | A | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+5326T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39233667 | ||||||
chr9:39233751 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+5242C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39233751 | ||||||
chr9:39233895 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+5098C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39233895 | ||||||
chr9:39234057 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+4936C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234057 | ||||||
chr9:39234118 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+4875G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234118 | ||||||
chr9:39234139 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+4854A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234139 | ||||||
chr9:39234156 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+4837G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234156 | ||||||
chr9:39234347 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+4646C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234347 | ||||||
chr9:39234408 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+4585G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39234408 | ||||||
chr9:39235069 | A | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+3924T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39235069 | ||||||
chr9:39236251 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+2742G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39236251 | ||||||
chr9:39236431 | T | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+2562A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39236431 | ||||||
chr9:39236518 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+2475A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39236518 | ||||||
chr9:39237077 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+1916T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39237077 | ||||||
chr9:39237315 | C | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+1678G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39237315 | ||||||
chr9:39237935 | C | CTTATTA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+1052_390+1057d others(8): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39237935 | ||||||
chr9:39238350 | CAAAA | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+639_390+642del others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238350 | ||||||
chr9:39238530 | AATAAAAA others(6): Show |
A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+450_390+462del others(13): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238530 | ||||||
chr9:39238532 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+461A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238532 | ||||||
chr9:39238539 | A | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+454T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238539 | ||||||
chr9:39238546 | A | AAAAC | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.390+443_390+446dup others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238546 | ||||||
chr9:39238550 | C | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+443G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238550 | ||||||
chr9:39238635 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+358T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238635 | ||||||
chr9:39238788 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+205T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238788 | ||||||
chr9:39238920 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.390+73T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 3/23 | chr9 | 39238920 | ||||||
chr9:39239375 | C | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-189G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39239375 | ||||||
chr9:39240105 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-919T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39240105 | ||||||
chr9:39240580 | A | AT | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-1395dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39240580 | ||||||
chr9:39240599 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-1413T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39240599 | ||||||
chr9:39240633 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-1447C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39240633 | ||||||
chr9:39241318 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-2132T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241318 | ||||||
chr9:39241485 | G | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-2299C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241485 | ||||||
chr9:39241676 | G | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-2490C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241676 | ||||||
chr9:39241681 | TG | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-2496delC | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241681 | ||||||
chr9:39241682 | G | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-2496C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241682 | ||||||
chr9:39241776 | CAA | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-2592_197-2591d others(4): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39241776 | ||||||
chr9:39242155 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-2969G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39242155 | ||||||
chr9:39242271 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-3085C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39242271 | ||||||
chr9:39242797 | C | CT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-3612dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39242797 | ||||||
chr9:39243210 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-4024A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39243210 | ||||||
chr9:39243376 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-4190C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39243376 | ||||||
chr9:39244191 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-5005T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39244191 | ||||||
chr9:39244405 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-5219T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39244405 | ||||||
chr9:39244543 | A | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-5357T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39244543 | ||||||
chr9:39244772 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-5586A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39244772 | ||||||
chr9:39244964 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-5778A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39244964 | ||||||
chr9:39245175 | A | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-5989T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39245175 | ||||||
chr9:39245866 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-6680A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39245866 | ||||||
chr9:39246192 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-7006G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39246192 | ||||||
chr9:39246210 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-7024A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39246210 | ||||||
chr9:39246576 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-7390G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39246576 | ||||||
chr9:39247004 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-7818T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39247004 | ||||||
chr9:39247143 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-7957G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39247143 | ||||||
chr9:39247571 | C | CTAT | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-8386_197-8385i others(5): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39247571 | ||||||
chr9:39247618 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-8432A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39247618 | ||||||
chr9:39247889 | C | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-8703G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39247889 | ||||||
chr9:39248368 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-9182G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248368 | ||||||
chr9:39248534 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-9348A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248534 | ||||||
chr9:39248556 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-9370G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248556 | ||||||
chr9:39248579 | C | CT | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-9394dupA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248579 | ||||||
chr9:39248838 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-9652G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248838 | ||||||
chr9:39248898 | G | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-9712C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248898 | ||||||
chr9:39248920 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-9734C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39248920 | ||||||
chr9:39249060 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-9874G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249060 | ||||||
chr9:39249285 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10099A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249285 | ||||||
chr9:39249409 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10223T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249409 | ||||||
chr9:39249575 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10389C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249575 | ||||||
chr9:39249579 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10393A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249579 | ||||||
chr9:39249619 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10433T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249619 | ||||||
chr9:39249692 | C | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10506G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249692 | ||||||
chr9:39249774 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-10588G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249774 | ||||||
chr9:39249926 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10740T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39249926 | ||||||
chr9:39250009 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10823A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250009 | ||||||
chr9:39250163 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-10977C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250163 | ||||||
chr9:39250228 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-11042A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250228 | ||||||
chr9:39250470 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-11284C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250470 | ||||||
chr9:39250775 | A | G | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-11589T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250775 | ||||||
chr9:39250829 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-11643T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250829 | ||||||
chr9:39250972 | T | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-11786A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39250972 | ||||||
chr9:39251039 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-11853C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251039 | ||||||
chr9:39251137 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-11951G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251137 | ||||||
chr9:39251183 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-11997C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251183 | ||||||
chr9:39251231 | G | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-12045C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251231 | ||||||
chr9:39251282 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-12096T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251282 | ||||||
chr9:39251528 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-12342G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251528 | ||||||
chr9:39251714 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-12528A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251714 | ||||||
chr9:39251975 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-12789C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39251975 | ||||||
chr9:39252379 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.197-13193A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39252379 | ||||||
chr9:39252491 | G | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-13305C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39252491 | ||||||
chr9:39252569 | T | A | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-13383A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39252569 | ||||||
chr9:39252935 | CAT | C | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-13751_197-1375 others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39252935 | ||||||
chr9:39253014 | TACACACA others(1): Show |
T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.197-13836_197-1382 others(12): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253014 | ||||||
chr9:39253145 | AAT | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+13749_196+1375 others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253145 | ||||||
chr9:39253163 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13733A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253163 | ||||||
chr9:39253165 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13731A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253165 | ||||||
chr9:39253167 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13729A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253167 | ||||||
chr9:39253255 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13641G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253255 | ||||||
chr9:39253548 | G | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13348C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253548 | ||||||
chr9:39253789 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+13107A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39253789 | ||||||
chr9:39254024 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+12872A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39254024 | ||||||
chr9:39254361 | G | GCACAGTC others(24): Show |
1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+12534_196+1253 others(35): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39254361 | ||||||
chr9:39254701 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+12195G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39254701 | ||||||
chr9:39255074 | T | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+11822A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255074 | ||||||
chr9:39255110 | C | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+11786G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255110 | ||||||
chr9:39255223 | C | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+11673G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255223 | ||||||
chr9:39255261 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+11635G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255261 | ||||||
chr9:39255661 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+11235C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255661 | ||||||
chr9:39255839 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+11057C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39255839 | ||||||
chr9:39256003 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+10893G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256003 | ||||||
chr9:39256185 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+10711C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256185 | ||||||
chr9:39256403 | A | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+10493T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256403 | ||||||
chr9:39256479 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+10417C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256479 | ||||||
chr9:39256505 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+10391T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256505 | ||||||
chr9:39256880 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+10016T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39256880 | ||||||
chr9:39257113 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+9783C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39257113 | ||||||
chr9:39257286 | C | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+9610G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39257286 | ||||||
chr9:39257306 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+9590G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39257306 | ||||||
chr9:39257411 | T | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+9485A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39257411 | ||||||
chr9:39257555 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+9341T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39257555 | ||||||
chr9:39258151 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+8745G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39258151 | ||||||
chr9:39258295 | G | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+8601C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39258295 | ||||||
chr9:39258460 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+8436T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39258460 | ||||||
chr9:39258673 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+8223G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39258673 | ||||||
chr9:39259184 | G | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+7712C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39259184 | ||||||
chr9:39259195 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+7701A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39259195 | ||||||
chr9:39259374 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+7522T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39259374 | ||||||
chr9:39259698 | A | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+7198T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39259698 | ||||||
chr9:39260267 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+6629A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260267 | ||||||
chr9:39260271 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+6625A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260271 | ||||||
chr9:39260501 | A | G | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+6395T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260501 | ||||||
chr9:39260614 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+6282A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260614 | ||||||
chr9:39260678 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+6218C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260678 | ||||||
chr9:39260749 | AAAC | A | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+6144_196+6146d others(5): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39260749 | ||||||
chr9:39261143 | G | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+5753C>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39261143 | ||||||
chr9:39261340 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+5556C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39261340 | ||||||
chr9:39261353 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+5543G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39261353 | ||||||
chr9:39262028 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+4868T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39262028 | ||||||
chr9:39263987 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+2909G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39263987 | ||||||
chr9:39264214 | G | GATAA | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+2678_196+2681d others(6): Show |
CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39264214 | ||||||
chr9:39264537 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+2359C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39264537 | ||||||
chr9:39265572 | T | TA | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+1323dupT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39265572 | ||||||
chr9:39266204 | T | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+692A>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39266204 | ||||||
chr9:39266530 | T | TA | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.196+365dupT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39266530 | ||||||
chr9:39266632 | A | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.196+264T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39266632 | ||||||
chr9:39266780 | A | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+116T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 2/23 | chr9 | 39266780 | ||||||
chr9:39267193 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-187A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39267193 | ||||||
chr9:39267725 | C | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.86-719G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39267725 | ||||||
chr9:39268730 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-1724A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39268730 | ||||||
chr9:39269005 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-1999G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39269005 | ||||||
chr9:39269261 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-2255G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39269261 | ||||||
chr9:39269582 | TA | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-2577delT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39269582 | ||||||
chr9:39270364 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-3358C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39270364 | ||||||
chr9:39270717 | C | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-3711G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39270717 | ||||||
chr9:39270862 | C | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-3856G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39270862 | ||||||
chr9:39271692 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-4686C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39271692 | ||||||
chr9:39271758 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-4752A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39271758 | ||||||
chr9:39272051 | C | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-5045G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272051 | ||||||
chr9:39272361 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-5355T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272361 | ||||||
chr9:39272536 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-5530C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272536 | ||||||
chr9:39272668 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-5662C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272668 | ||||||
chr9:39272884 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-5878G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272884 | ||||||
chr9:39272966 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-5960G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39272966 | ||||||
chr9:39273056 | C | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-6050G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39273056 | ||||||
chr9:39273079 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-6073A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39273079 | ||||||
chr9:39274275 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-7269G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39274275 | ||||||
chr9:39274313 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-7307A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39274313 | ||||||
chr9:39275003 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-7997T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39275003 | ||||||
chr9:39275005 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-7999G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39275005 | ||||||
chr9:39275407 | A | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-8401T>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39275407 | ||||||
chr9:39275817 | G | A | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-8811C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39275817 | ||||||
chr9:39276013 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-9007G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39276013 | ||||||
chr9:39276025 | T | C | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-9019A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39276025 | ||||||
chr9:39276458 | C | T | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.86-9452G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39276458 | ||||||
chr9:39276629 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-9623C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39276629 | ||||||
chr9:39276681 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-9675A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39276681 | ||||||
chr9:39277173 | G | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-10167C>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39277173 | ||||||
chr9:39277849 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+10131G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39277849 | ||||||
chr9:39277887 | T | C | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+10093A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39277887 | ||||||
chr9:39277916 | C | T | 2 | a0002c0003t0004g0001a0004c0002t0001g0003 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+10064G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39277916 | ||||||
chr9:39278481 | C | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+9499G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39278481 | ||||||
chr9:39278690 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+9290A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39278690 | ||||||
chr9:39278973 | T | C | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+9007A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39278973 | ||||||
chr9:39279509 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+8471T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39279509 | ||||||
chr9:39279525 | A | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+8455T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39279525 | ||||||
chr9:39279910 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+8070C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39279910 | ||||||
chr9:39280109 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+7871A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39280109 | ||||||
chr9:39280344 | A | G | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+7636T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39280344 | ||||||
chr9:39280441 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+7539G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39280441 | ||||||
chr9:39280721 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+7259A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39280721 | ||||||
chr9:39281080 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+6900C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39281080 | ||||||
chr9:39281115 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+6865C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39281115 | ||||||
chr9:39281402 | T | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+6578A>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39281402 | ||||||
chr9:39283832 | GT | G | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+4147delA | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39283832 | ||||||
chr9:39284101 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+3879G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39284101 | ||||||
chr9:39285048 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2932A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285048 | ||||||
chr9:39285517 | A | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2463T>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285517 | ||||||
chr9:39285591 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+2389C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285591 | ||||||
chr9:39285742 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2238G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285742 | ||||||
chr9:39285869 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2111A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285869 | ||||||
chr9:39285897 | T | C | 1 | a0002c0003t0004g0001 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+2083A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285897 | ||||||
chr9:39285898 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2082G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285898 | ||||||
chr9:39285939 | A | T | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+2041T>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39285939 | ||||||
chr9:39286146 | C | T | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+1834G>A | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39286146 | ||||||
chr9:39286535 | G | A | 3 | a0001c0001t0003g0002a0002c0003t0004g0001a0004c0002t0001g0003 | 3 | HG02109.hp1 HG02109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.85+1445C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39286535 | ||||||
chr9:39286551 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+1429C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39286551 | ||||||
chr9:39286568 | G | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+1412C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39286568 | ||||||
chr9:39287101 | C | A | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+879G>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39287101 | ||||||
chr9:39287145 | T | C | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+835A>G | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39287145 | ||||||
chr9:39287247 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+733C>T | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39287247 | ||||||
chr9:39287676 | C | G | 1 | a0004c0002t0001g0003 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+304G>C | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39287676 | ||||||
chr9:39287914 | TA | T | 2 | a0001c0001t0003g0002a0002c0003t0004g0001 | 2 | HG02109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.85+65delT | CNTNAP3 | ENSG00000106714.18 | transcript | ENST00000297668.11 | protein_coding | 1/23 | chr9 | 39287914 |