http://identifiers.org/hco/14/GRCh38#96392184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105672450-C-A

96392184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105672450-C-G

96392184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105672450-C-T

96392322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672578-G-A

96392322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672578-G-T

96397440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675928-G-A

96397966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676299-G-A

96397966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676299-G-T

96398057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676386-A-G

96398086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105676415-C-T

96398104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105676433-G-A

96398104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105676433-G-C

96398122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105676451-G-A

96398122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105676451-G-C

96398217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105676549-C-G

96398341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676672-T-A

96398341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676672-T-C

96398349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676680-G-A

http://identifiers.org/hco/14/GRCh38#96398356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105676688-C-A

96398356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676688-C-T

96398364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676696-T-C

96398378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676717-G-A

96398378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105676717-G-T

96398461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105677394-T-C

96398506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105677439-C-G

96404638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679666-G-A

96404638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679666-G-T

96404647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679675-G-A

96404647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679675-G-T

96404652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679680-A-T

96404671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679700-G-A

96404671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679700-G-T

96404728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679733-T-C

http://identifiers.org/hco/14/GRCh38#96404759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105679764-C-A

96404759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 105679764-C-T

http://identifiers.org/hco/14/GRCh38#96404762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105679767-C-A

96404795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105679800-G-A

96404822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105679827-T-C

96404864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 105679869-T-C

96404864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 105679869-T-G

96404894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679928-G-A

96404894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679928-G-T

http://identifiers.org/hco/14/GRCh38#96404911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105679946-C-A

96404911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679946-C-T

96404912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679947-T-A

96404912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679947-T-C

96404946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105679978-A-G

96404977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105680016-G-A

96404977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105680016-G-T

96404984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105680023-A-G

http://identifiers.org/hco/14/GRCh38#96407099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105680918-A-C

96407100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105680919-G-C

96407254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105681067-C-T

96407255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105681068-T-C

96408838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682235-G-A

http://identifiers.org/hco/14/GRCh38#96408843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105682240-A-C

96408843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105682240-A-G

96409031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682362-T-C

96409032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682363-G-A

http://identifiers.org/hco/14/GRCh38#96409041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105682372-C-A

http://identifiers.org/hco/14/GRCh38#96409042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105682373-A-C

96409042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682373-A-G

96409048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682379-G-A

http://identifiers.org/hco/14/GRCh38#96409053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105682384-C-A

96409053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105682384-C-T

96415962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105686000-G-A

96416404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105686463-T-A

96416459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105686497-A-G

96416486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105686524-A-G

96416715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105686922-G-C

96416783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105687004-C-G

96417001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105687169-G-T

96417278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105687505-A-G

96418012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105689214-T-G

96420819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105692443-T-A

96420819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105692443-T-C

96420824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 105692448-G-A

96420830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105692454-T-C

96420942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105692576-G-A

96420990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105692713-G-A

96420990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105692713-G-T

96421276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105692960-G-A

96421360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105693191-T-C

96421379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105693210-C-T

96421415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 105693246-A-G

96421445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105693277-A-G

96421537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105693370-C-T

http://identifiers.org/hco/14/GRCh38#96421583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105693403-C-A

96421583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105693403-C-G

96421591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105693411-T-C

http://identifiers.org/hco/14/GRCh38#96437734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105699576-C-A

96437734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105699576-C-T

96437754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105699596-A-G

96437819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105699675-G-A

96437819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105699675-G-C

96437819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105699675-G-T

96437904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105699761-A-G

96442762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105701181-A-G

96442833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701252-A-G

96442836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701255-G-C

http://identifiers.org/hco/14/GRCh38#96442847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105701266-C-A

96442861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701274-A-G

96442861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701274-A-T

96442954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701307-T-C

96443024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701320-C-T

96443063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105701361-C-T

http://identifiers.org/hco/14/GRCh38#96443173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105701456-C-A

96446315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704642-A-G

96446443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704768-G-A

96446443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704768-G-T

96446450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704775-G-T

96446507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704823-G-A

96446509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105704825-G-A

96446509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105704825-G-T

96446541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105704857-C-T

96446651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105704961-G-C

96449786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707252-G-A

96449786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707252-G-T

http://identifiers.org/hco/14/GRCh38#96449911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105707379-C-A

96449911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707379-C-G

96449911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707379-C-T

96450245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707620-T-C

http://identifiers.org/hco/14/GRCh38#96450262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105707663-C-A

96450280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707696-G-T

http://identifiers.org/hco/14/GRCh38#96450422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105707814-A-C

96450422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707814-A-T

96450433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105707825-A-T

96451292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708381-G-T

96451293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708382-G-T

96451310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708397-G-A

96451360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708446-T-C

96451361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708447-G-C

96451361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708447-G-T

96451366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708452-G-C

96451366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708452-G-T

96451441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105708515-A-G

http://identifiers.org/hco/14/GRCh38#96451447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105708521-C-A

96451456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105708530-A-G

96451499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105708573-G-A

96451499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105708573-G-C

96451531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105708605-C-T

96451557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105708631-G-A

96451575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708649-C-T

96451596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708672-A-G

96451656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708732-G-T

http://identifiers.org/hco/14/GRCh38#96451667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105708739-C-A

96451667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708739-C-T

96451687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708759-A-G

http://identifiers.org/hco/14/GRCh38#96451712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105708782-C-A

96451714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708783-A-T

96451719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105708788-T-G

96453937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709056-T-G

96453967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709064-G-A

96454155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709179-C-T

96454553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709526-C-G

96454608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709575-C-T

96454609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105709576-A-G

96456256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105711389-A-G

96456256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105711389-A-T

96456278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105711411-A-G

96456373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105711489-C-T

96457942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713315-G-A

96457942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713315-G-T

http://identifiers.org/hco/14/GRCh38#96457944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105713317-A-C

http://identifiers.org/hco/14/GRCh38#96457961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105713334-C-A

96457961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713334-C-T

http://identifiers.org/hco/14/GRCh38#96458011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105713376-C-A

96458011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713376-C-T

96458106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105713468-T-A

96458106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105713468-T-C

96458128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105713490-G-A

96458128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105713490-G-T

http://identifiers.org/hco/14/GRCh38#96458130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105713492-C-A

96458130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105713492-C-G

96458130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105713492-C-T

96458208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105713570-T-C

96458239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713611-G-A

96458239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713611-G-T

http://identifiers.org/hco/14/GRCh38#96458273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105713637-C-A

96458273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105713637-C-T

96460685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105714697-C-G

96460792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105718991-G-T

http://identifiers.org/hco/14/GRCh38#96462319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105720150-A-C

96462400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, undefined
orthologous variants: 105720248-T-G

96462477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105720321-G-A

96462522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, undefined
orthologous variants: 105720367-C-T

96468824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105720631-C-T

96468997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105722605-C-G

96469732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105723549-G-A

96469788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105723601-G-C

96469960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105723788-G-A

96470376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105724085-A-G

96470391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105724098-A-G

http://identifiers.org/hco/14/GRCh38#96470433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105724137-C-A

96470433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105724137-C-T

96471363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727610-G-A

96471363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727610-G-C

96471363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727610-G-T

96471373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727620-A-G

96471373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727620-A-T

96471430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727679-G-A

96471430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727679-G-T

http://identifiers.org/hco/14/GRCh38#96471447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105727701-A-C

96471650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105727903-T-C

http://identifiers.org/hco/14/GRCh38#96472572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105729608-C-A

96472572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105729608-C-G

96472572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105729608-C-T

96472591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105729627-A-G

96472591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105729627-A-T

http://identifiers.org/hco/14/GRCh38#96472670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105730195-A-C

96472725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, missense_variant
orthologous variants: 105730250-A-G

96478222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732614-A-G

http://identifiers.org/hco/14/GRCh38#96478319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105732687-C-A

96478319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732687-C-T

96478362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732716-A-G

96478407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732772-A-G

96478447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732793-G-A

96478447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732793-G-C

96478456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105732802-T-C

96478734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733063-A-T

96478737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733066-G-T

96478769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733097-A-G

96478771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733101-G-A

96478771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733101-G-T

96479539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105733377-C-T

96482833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105734640-G-A

96482833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105734640-G-T

96482873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105734680-A-G

96482916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105734713-A-T

96482921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105734718-A-G

96482983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, missense_variant
orthologous variants: 105734773-C-T

96483078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: synonymous variant
orthologous variants: 105734868-T-C

96483163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105734953-C-T

96483164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105734954-G-A

96483164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: missense variant
orthologous variants: 105734954-G-T

96483380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105735086-T-A

96486767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105746953-T-C

http://identifiers.org/hco/14/GRCh38#96486835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747013-C-A

96486835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747013-C-T

96486836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747014-T-A

96486836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747014-T-C

96486836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747014-T-G

http://identifiers.org/hco/14/GRCh38#96486851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747061-C-A

http://identifiers.org/hco/14/GRCh38#96486859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747069-C-A

96486859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747069-C-T

http://identifiers.org/hco/14/GRCh38#96486864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747074-C-A

96486864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747074-C-T

96486873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747083-T-C

http://identifiers.org/hco/14/GRCh38#96486889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747097-C-A

96486889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747097-C-T

http://identifiers.org/hco/14/GRCh38#96486891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747099-A-C

96486891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105747099-A-G

96486891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105747099-A-T

96486904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: stop gained
orthologous variants: 105747115-C-T

96487104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747323-G-A

96487104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747323-G-T

http://identifiers.org/hco/14/GRCh38#96487114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747338-C-A

96487114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747338-C-G

96487114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747338-C-T

96487143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747365-G-A

96487143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747365-G-T

http://identifiers.org/hco/14/GRCh38#96487178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747404-C-A

96487486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747635-G-A

96487585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747726-C-T

http://identifiers.org/hco/14/GRCh38#96487586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747727-C-A

96487586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747727-C-T

96487590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: intron variant
orthologous variants: 105747731-G-A

96488307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 105747932-A-G

http://identifiers.org/hco/14/GRCh38#96488352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747977-A-C

96488366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105747991-C-T

http://identifiers.org/hco/14/GRCh38#96488369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105747994-C-A

http://identifiers.org/hco/14/GRCh38#96488375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105748000-C-A

96488375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748000-C-T

96488444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748064-T-A

96488473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748122-A-G

96488534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748189-T-C

96488534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748189-T-G

96488543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20091
most severe consequence: 3 prime UTR variant
orthologous variants: 105748195-A-G