http://identifiers.org/hco/19/GRCh38#17601543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72079610-C-A

17601789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079789-C-T

17601798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079799-T-A

17601798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079799-T-C

17601846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079843-C-G

17601846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079843-C-T

17601894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079888-G-T

17601932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72079922-C-T

http://identifiers.org/hco/19/GRCh38#17601933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72079923-C-A

http://identifiers.org/hco/19/GRCh38#17602474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72080331-C-A

17602474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080331-C-T

17602492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080347-G-C

17602492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080347-G-T

http://identifiers.org/hco/19/GRCh38#17602827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72080663-C-A

17602949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080781-G-T

17602992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080822-G-A

17602992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080822-G-T

17603018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080849-A-G

17603067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080901-T-C

17603090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080924-G-T

17603181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72080999-T-C

17603238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72081056-G-A

17603238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72081056-G-T

http://identifiers.org/hco/19/GRCh38#17603244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72081062-C-A

http://identifiers.org/hco/19/GRCh38#17603312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#72081102-C-A

http://identifiers.org/hco/19/GRCh38#17603330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72081119-C-A

17603449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72081221-C-T

17603646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72081396-G-C

17605042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72081552-C-G

17605882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 3 prime UTR variant
orthologous variants: 72082033-A-G

17606171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: 72082184-G-A

17606171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: 72082184-G-T

http://identifiers.org/hco/19/GRCh38#17606174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#72082187-C-A

17606174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: 72082187-C-T

http://identifiers.org/hco/19/GRCh38#17606440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#72082436-C-A

17606440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72082436-C-T

17606529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72082525-T-G

17606536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72082532-G-T

17609444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72082733-C-G

17609448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72082737-G-A

17609877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72083126-G-T

http://identifiers.org/hco/19/GRCh38#17609999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72083219-C-A

17610131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72083347-A-G

17611611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72083468-G-C

17611611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72083468-G-T

17611974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72083795-G-A

17611974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72083795-G-T

http://identifiers.org/hco/19/GRCh38#17614292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72084854-C-A

17614292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72084854-C-T

http://identifiers.org/hco/19/GRCh38#17614296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72084859-C-A

17614296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72084859-C-T

17614362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72084922-A-G

http://identifiers.org/hco/19/GRCh38#17614521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72085085-C-A

http://identifiers.org/hco/19/GRCh38#17614527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72085091-A-C

17614527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085091-A-G

17614530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085094-C-T

http://identifiers.org/hco/19/GRCh38#17614531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72085100-C-A

17614531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085100-C-T

17615087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085562-G-A

17616087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085810-G-A

17616087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085810-G-C

17616172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085904-T-C

17616292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085973-C-G

17616292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72085973-C-T

17616359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086038-G-A

17616359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086038-G-T

http://identifiers.org/hco/19/GRCh38#17616381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72086060-C-A

17616381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086060-C-T

http://identifiers.org/hco/19/GRCh38#17616504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72086181-A-C

17616504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086181-A-G

17616504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086181-A-T

17616533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086210-T-C

17616533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086210-T-G

17616613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086302-A-T

17616878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086527-C-T

17617363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72086939-T-C

17617535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087066-C-T

17617715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72087174-C-T

17618550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087654-T-C

http://identifiers.org/hco/19/GRCh38#17618821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72087798-C-A

17618821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087798-C-T

17618829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72087806-C-T

http://identifiers.org/hco/19/GRCh38#17619187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72088102-C-A

17619187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72088102-C-T

17619267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72088193-T-C

17620045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72088566-C-T

http://identifiers.org/hco/19/GRCh38#17620401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72088907-A-C

17620402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72088908-C-T

http://identifiers.org/hco/19/GRCh38#17620513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72089018-A-C

17620546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089047-G-A

17620546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089047-G-C

17620546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089047-G-T

17620564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089065-G-T

17620603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089102-G-A

17620603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089102-G-C

17620603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089102-G-T

17620771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72089260-G-T

17621651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72090253-T-C

17621802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72090386-A-G

17621908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72090508-G-A

17622075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72090755-G-C

17622075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72090755-G-T

17622562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091205-A-T

17622632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091265-T-A

17622866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091391-A-G

17622939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091444-T-A

17622968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091465-T-C

17622978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091475-G-A

17622978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091475-G-T

17623028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091506-G-A

17623028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091506-G-C

17623028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091506-G-T

17623041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091519-G-A

17623041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091519-G-C

17623041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091519-G-T

17623183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091578-A-G

17623282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091652-G-A

17623282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091652-G-T

17623315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72091678-C-T

17623481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72091787-T-A

17623481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72091787-T-C

17624744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092267-C-G

17624744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092267-C-T

17624762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092285-C-T

http://identifiers.org/hco/19/GRCh38#17624764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72092287-A-C

17624847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72092362-C-G

17624847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72092362-C-T

17624856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72092371-G-A

17624982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092497-G-A

17624997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092511-A-T

17625071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092566-G-T

17625089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092575-G-C

17625089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092575-G-T

17625190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092599-C-T

17625485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72092844-C-T

http://identifiers.org/hco/19/GRCh38#17625511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72092870-C-A

17625668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093060-T-A

17625669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093061-C-T

17625703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093076-T-C

17625716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093089-T-C

17625747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093120-T-A

http://identifiers.org/hco/19/GRCh38#17625828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093188-C-A

17625842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093202-C-T

17625897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093257-T-A

17625897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093257-T-C

17625952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093312-G-T

17625966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093326-C-T

17626016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093368-A-G

17626021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093373-T-G

17626080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093432-T-A

http://identifiers.org/hco/19/GRCh38#17626174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093510-C-A

17626195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093532-T-A

17626199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093536-T-A

17626199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093536-T-G

http://identifiers.org/hco/19/GRCh38#17626200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093537-C-A

17626200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093537-C-T

http://identifiers.org/hco/19/GRCh38#17626203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093540-A-C

17626207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093544-T-C

http://identifiers.org/hco/19/GRCh38#17626212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093549-C-A

17626212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093549-C-T

17626215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093552-G-A

17626215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093552-G-C

17626215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093552-G-T

http://identifiers.org/hco/19/GRCh38#17626228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093565-A-C

17626228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093565-A-G

17626235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093572-T-C

17626257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093594-T-A

17626259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093596-T-C

17626268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093605-A-T

17626269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093606-C-T

17626278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093615-A-G

17626278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72093615-A-T

http://identifiers.org/hco/19/GRCh38#17626281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093618-C-A

17626292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093629-T-G

17626328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093656-T-A

17626328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093656-T-C

17626328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093656-T-G

17626330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093658-T-G

http://identifiers.org/hco/19/GRCh38#17626348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093673-C-A

17626348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093673-C-T

17626356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093681-T-A

17626356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093681-T-C

http://identifiers.org/hco/19/GRCh38#17626381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093706-C-A

17626381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093706-C-T

http://identifiers.org/hco/19/GRCh38#17626394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093719-C-A

17626394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093719-C-T

http://identifiers.org/hco/19/GRCh38#17626452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72093774-C-A

17626452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093774-C-T

17626488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093808-T-C

17626519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093841-T-C

17626571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093898-G-A

17626571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72093898-G-T

http://identifiers.org/hco/19/GRCh38#17627074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72094236-C-A

17627122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094277-C-T

17627129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094280-G-A

http://identifiers.org/hco/19/GRCh38#17627159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72094299-C-A

17627159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094299-C-G

17627159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094299-C-T

17627319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094349-C-T

17627620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094593-A-G

17627667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094625-G-T

17627680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094638-G-A

17627680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094638-G-C

17627680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094638-G-T

17627692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094648-G-A

17627692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094648-G-T

17627700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094657-G-A

17627700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72094657-G-T

17628114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72094953-T-A

17628133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72094972-T-C

17628133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72094972-T-G

17628186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72095014-G-A

17628186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72095014-G-C

17628186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 72095014-G-T

http://identifiers.org/hco/19/GRCh38#17628364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72095156-A-C

http://identifiers.org/hco/19/GRCh38#17628365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72095157-C-A

http://identifiers.org/hco/19/GRCh38#17628423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72095200-C-A

17628423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095200-C-T

17629224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095720-G-A

17629288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72095784-G-A

17629288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72095784-G-T

17629345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095837-G-A

17629345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095837-G-C

17629345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095837-G-T

17629374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095867-G-A

http://identifiers.org/hco/19/GRCh38#17629379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72095872-A-C

http://identifiers.org/hco/19/GRCh38#17629386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72095881-C-A

17629386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72095881-C-T

http://identifiers.org/hco/19/GRCh38#17630012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72097082-C-A

http://identifiers.org/hco/19/GRCh38#17630044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72097109-A-C

http://identifiers.org/hco/19/GRCh38#17630069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72097134-C-A

17630069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72097134-C-T

17630422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72097384-A-G

http://identifiers.org/hco/19/GRCh38#17630423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72097385-C-A

17630506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72097450-G-T

17630508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72097452-T-C

17630657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72097520-A-G

http://identifiers.org/hco/19/GRCh38#17636016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72100537-C-A

17636155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 72100676-G-A

17636155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 72100676-G-T

17639113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72101572-T-C

17639663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102345-G-A

17639663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102345-G-C

17639663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102345-G-T

http://identifiers.org/hco/19/GRCh38#17639675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72102357-C-A

17639675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102357-C-T

17639716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102387-T-C

17639716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102387-T-G

17639779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102444-T-C

http://identifiers.org/hco/19/GRCh38#17640004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72102684-C-A

17640004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102684-C-T

http://identifiers.org/hco/19/GRCh38#17640036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72102692-A-C

17640036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102692-A-G

17640036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102692-A-T

17640290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72102982-C-T

17640318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103009-C-T

17640383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103090-A-G

http://identifiers.org/hco/19/GRCh38#17640410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72103116-C-A

17640410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103116-C-T

http://identifiers.org/hco/19/GRCh38#17640437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72103137-A-C

17640670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103330-A-G

17640847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103434-T-C

http://identifiers.org/hco/19/GRCh38#17641309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72103695-C-A

17641309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72103695-C-G

17641467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72103842-G-A

17641503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72103878-T-C

17642242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72104045-A-G

17642306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72104109-T-C

17642339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72104146-C-G

17642720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72104508-A-G

17642890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72104642-C-T

17642899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72104651-G-T

17642950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72104702-A-G

17642972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72104730-A-G

17645882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72105086-G-A

17646157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72105344-G-T

17646183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72105370-A-G

17647302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72106069-G-A

http://identifiers.org/hco/19/GRCh38#17647326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72106093-C-A

17647347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72106114-C-T

17647407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72106174-C-G

17647407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72106174-C-T

17647449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72106216-T-C

17647505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106277-G-A

17647505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106277-G-C

17647505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106277-G-T

17647539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106319-T-C

17647539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106319-T-G

http://identifiers.org/hco/19/GRCh38#17647555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72106335-C-A

17647555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106335-C-G

17647555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106335-C-T

17647597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106366-T-C

17647608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106378-A-G

17647691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106489-C-T

17647996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106861-T-C

17648022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106887-T-A

17648022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106887-T-C

17648022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72106887-T-G

17648183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107165-C-G

http://identifiers.org/hco/19/GRCh38#17648201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107176-A-C

http://identifiers.org/hco/19/GRCh38#17648203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107177-A-C

17648204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107178-G-A

17648324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107320-C-T

17648329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107328-T-A

17648329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107328-T-C

17648329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107328-T-G

http://identifiers.org/hco/19/GRCh38#17648367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107379-C-A

17648367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107379-C-G

17648367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107379-C-T

17648405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107415-G-T

http://identifiers.org/hco/19/GRCh38#17648408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107418-C-A

17648408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107418-C-G

17648558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: 72107575-C-G

17648558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous_variant, undefined
orthologous variants: 72107575-C-T

17648576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72107593-T-C

17648758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107715-T-C

http://identifiers.org/hco/19/GRCh38#17648763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107720-C-A

17648763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107720-C-T

http://identifiers.org/hco/19/GRCh38#17648778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72107729-C-A

17649006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107864-A-G

17649099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72107961-T-G

17649327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108135-G-A

17649327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108135-G-T

17649413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108217-C-T

17649427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108231-T-A

17649427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108231-T-C

17649577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: 72108375-C-T

17649612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108410-G-C

17652559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108829-G-A

17652559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72108829-G-T

17652782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109046-C-T

17652905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109147-G-A

17652908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109150-C-T

17653928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109299-G-A

17654063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109465-G-A

17654110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72109518-A-G

17654891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72110284-T-C

17655158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: 72110524-G-T

17655175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: 72110541-G-A

17655175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: 72110541-G-T

http://identifiers.org/hco/19/GRCh38#17655214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#72110582-C-A

17655214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: 72110582-C-T

17655216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron_variant, undefined
orthologous variants: 72110584-T-G

http://identifiers.org/hco/19/GRCh38#17655328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#72110701-C-A

17655328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense_variant, undefined
orthologous variants: 72110701-C-G

http://identifiers.org/hco/19/GRCh38#17655343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72110716-C-A

17655343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72110716-C-T

http://identifiers.org/hco/19/GRCh38#17655903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72110920-C-A

17655903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72110920-C-T

http://identifiers.org/hco/19/GRCh38#17655963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72110980-C-A

17656329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72111376-G-A

17656329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: 72111376-G-C

17656329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: 72111376-G-T

17656414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72111458-A-T

17658073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72113097-T-A

17658306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72113328-A-G

http://identifiers.org/hco/19/GRCh38#17663465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72114426-C-A

17663465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72114426-C-T

http://identifiers.org/hco/19/GRCh38#17663637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72114523-C-A

17663657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72114543-A-T

17663663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72114549-T-C

17666559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115056-G-A

17666559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115056-G-T

http://identifiers.org/hco/19/GRCh38#17666579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72115071-A-C

17666579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115071-A-G

17666580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115072-G-A

17666580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115072-G-C

17666580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115072-G-T

http://identifiers.org/hco/19/GRCh38#17666636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72115111-C-A

17666636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115111-C-T

17666717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115192-A-G

17668212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115597-T-C

17669701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115950-T-C

17669702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115951-G-T

17669725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72115965-A-G

http://identifiers.org/hco/19/GRCh38#17669744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72116011-C-A

17669744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72116011-C-G

http://identifiers.org/hco/19/GRCh38#17669767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72116043-C-A

17669767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72116043-C-T

http://identifiers.org/hco/19/GRCh38#17672550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72116965-C-A

17672564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72116979-G-T

http://identifiers.org/hco/19/GRCh38#17672602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72117017-C-A

17672602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72117017-C-G

17674701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: synonymous variant
orthologous variants: 72118667-G-A

17674701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: missense variant
orthologous variants: 72118667-G-C

17675976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119237-A-G

17675976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119237-A-T

17676072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119345-G-A

17676072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119345-G-C

17676135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119385-G-A

17676135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119385-G-T

17676286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119473-G-A

17676286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119473-G-C

17676483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72119609-C-T

http://identifiers.org/hco/19/GRCh38#17686084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72122980-A-C

17686155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72123053-T-A

17686180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72123090-C-T

17687030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72123662-T-G

17687092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72123720-C-G

17687306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: 72123894-C-G

http://identifiers.org/hco/19/GRCh38#17687359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72123936-A-C

http://identifiers.org/hco/19/GRCh38#17688130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#72124244-C-A

17688235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 5 prime UTR variant
orthologous variants: 72124319-G-A

17688235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23150
most severe consequence: 5 prime UTR variant
orthologous variants: 72124319-G-T