73571569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90747921-A-T

73571720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748056-A-G

73571955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748293-C-T

73572167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748482-T-C

http://identifiers.org/hco/4/GRCh38#73572186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90748507-C-A

http://identifiers.org/hco/4/GRCh38#73572219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90748543-C-A

http://identifiers.org/hco/4/GRCh38#73572283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90748597-C-A

73572299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748611-A-G

73572334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748638-G-A

73572335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748639-T-C

73572396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748672-T-C

73572432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748692-G-T

73572561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748808-T-C

73572774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90748967-T-C

73572844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749027-T-C

73572845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749028-G-A

http://identifiers.org/hco/4/GRCh38#73573696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749381-C-A

73573819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749462-G-A

73573819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749462-G-T

73573860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 90749495-T-C

http://identifiers.org/hco/4/GRCh38#73573932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749563-C-A

73573932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749563-C-G

73573932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749563-C-T

73573994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749611-A-G

73573995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749612-G-T

73573998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749615-G-A

73574021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749638-T-C

http://identifiers.org/hco/4/GRCh38#73574038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749655-C-A

73574038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749655-C-G

73574038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749655-C-T

http://identifiers.org/hco/4/GRCh38#73574055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749676-C-A

73574055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749676-C-G

73574055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749676-C-T

73574069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749690-G-T

73574085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749706-G-A

http://identifiers.org/hco/4/GRCh38#73574106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749725-C-A

73574106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749725-C-G

73574106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749725-C-T

73574133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749751-G-A

73574158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749776-G-T

http://identifiers.org/hco/4/GRCh38#73574168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749786-C-A

73574624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749890-A-G

73574668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90749930-A-T

http://identifiers.org/hco/4/GRCh38#73574712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90749972-C-A

73574761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750020-A-G

73574909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750259-T-G

73575018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750365-G-A

73575025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750372-T-C

http://identifiers.org/hco/4/GRCh38#73575069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90750425-C-A

73575075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750431-T-C

73575184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750509-A-G

73575185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750510-G-A

http://identifiers.org/hco/4/GRCh38#73575220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90750544-A-C

http://identifiers.org/hco/4/GRCh38#73575372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90750665-A-C

73575372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750665-A-T

73575454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750738-T-C

73575461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750745-G-T

73575479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750777-G-A

http://identifiers.org/hco/4/GRCh38#73575494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90750797-C-A

73575548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90750851-T-A

73575626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751060-G-A

73575626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751060-G-T

73575628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751062-G-T

http://identifiers.org/hco/4/GRCh38#73575809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90751333-A-C

73575815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751339-T-C

73576107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751630-G-A

73576107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3 prime UTR variant
orthologous variants: 90751630-G-T

73576251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 90751748-G-T

73576535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90752007-A-G

73576596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90752088-G-T

73576670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: synonymous variant
orthologous variants: 90752162-A-G

http://identifiers.org/hco/4/GRCh38#73576981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90753017-C-A

73577269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90753273-A-G

73577305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90753295-C-G

73577458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90753435-A-G

73577460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90753437-C-T

73577609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90753516-T-C

http://identifiers.org/hco/4/GRCh38#73577729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90753625-C-A

73581667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754049-G-C

73581667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754049-G-T

73581734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754207-G-A

73581734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754207-G-T

73581741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754214-G-A

73581741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754214-G-T

http://identifiers.org/hco/4/GRCh38#73581763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90754236-C-A

73581763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754236-C-T

73582052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754491-A-G

73582079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754525-T-C

http://identifiers.org/hco/4/GRCh38#73582081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90754527-C-A

73582081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754527-C-T

73582115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754560-G-A

73582115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754560-G-T

73582153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754598-A-G

73582169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754615-A-G

http://identifiers.org/hco/4/GRCh38#73582224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#90754670-C-A

73582224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, missense_variant
orthologous variants: 90754670-C-T

73582311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754760-T-A

73582311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754760-T-C

73582341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754789-T-C

http://identifiers.org/hco/4/GRCh38#73582347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90754795-A-C

73582347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90754795-A-G

73584395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755150-C-T

73584694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755418-G-A

73584741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755457-T-A

http://identifiers.org/hco/4/GRCh38#73584754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90755466-A-C

73584754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755466-A-G

73584775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755485-T-C

73584783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755493-A-G

73584783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755493-A-T

73584797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 90755506-T-C

73584879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90755590-G-C

73584955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90755656-G-A

73584998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90755700-T-A

73585078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756568-G-A

73585078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756568-G-T

http://identifiers.org/hco/4/GRCh38#73585090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90756580-A-C

73585090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756580-A-G

73585090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756580-A-T

73585135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756622-G-A

73585135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756622-G-C

73585135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756622-G-T

73585165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756647-T-C

73585312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: synonymous variant
orthologous variants: 90756802-T-A

73585312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: synonymous variant
orthologous variants: 90756802-T-C

73585429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756916-T-A

73585429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756916-T-G

73585434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756921-T-C

73585490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90756969-A-G

http://identifiers.org/hco/4/GRCh38#73585618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90757076-C-A

73585618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757076-C-T

73585624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757082-T-C

73586100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757337-G-A

73586113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757350-T-C

73587711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757474-A-G

73587749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757503-G-T

http://identifiers.org/hco/4/GRCh38#73587820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90757554-A-C

73587845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: missense variant
orthologous variants: 90757579-T-C

http://identifiers.org/hco/4/GRCh38#73587970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90757708-C-A

73587970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757708-C-T

73587975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757713-A-T

http://identifiers.org/hco/4/GRCh38#73587997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90757721-C-A

73587997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757721-C-T

73588015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757739-T-C

73588015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757739-T-G

73588030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757752-G-A

73588030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90757752-G-T

73588552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90758244-C-T

73588607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90758304-T-A

http://identifiers.org/hco/4/GRCh38#73589072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90758854-C-A

73589072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90758854-C-G

73589115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90758895-A-G

73589315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759112-T-G

73589443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759237-C-T

73589694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759532-T-A

73589725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759563-G-A

73589781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759618-C-T

73589861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759691-G-A

http://identifiers.org/hco/4/GRCh38#73589893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90759723-C-A

73589908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759738-A-T

73590149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90759994-G-T

73590325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760165-T-C

73590367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760203-G-A

73590380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760227-A-G

73590382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760229-A-G

73590438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760274-A-G

73590527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90760367-T-C

73590602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90760443-C-T

73591540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762058-C-T

73591586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762094-A-G

73591833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762330-C-T

73591895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762454-T-A

73591990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762548-A-T

73592160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762715-T-A

http://identifiers.org/hco/4/GRCh38#73592163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90762718-C-A

73592163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762718-C-T

73592222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762774-T-C

73592409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90762957-G-A

73592587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763094-G-T

73592696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763203-T-C

73592864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763363-G-A

http://identifiers.org/hco/4/GRCh38#73592888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90763387-C-A

73592888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763387-C-T

73592922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763419-A-G

73592945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763442-T-C

73593010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763504-G-A

73593015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90763509-T-G

73593227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763539-G-C

73593393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763602-A-G

http://identifiers.org/hco/4/GRCh38#73593409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90763618-A-C

73593426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763632-A-G

73593426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763632-A-T

http://identifiers.org/hco/4/GRCh38#73593440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90763643-A-C

http://identifiers.org/hco/4/GRCh38#73593614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90763813-C-A

73593614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763813-C-G

73593614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763813-C-T

73593630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763834-T-C

73593649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763854-A-G

73593649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763854-A-T

73593650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763855-T-C

73593652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763857-T-C

73593666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763872-T-A

73593666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763872-T-G

73593716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763920-G-A

73593716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763920-G-T

73593719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763924-G-T

73593736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763941-T-C

73593740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763945-T-C

73593768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90763973-T-C

73593952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90764151-C-T

73594072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90764264-G-A

73598200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765060-C-T

73598216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765076-T-A

http://identifiers.org/hco/4/GRCh38#73598284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90765141-C-A

73598418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765252-C-T

http://identifiers.org/hco/4/GRCh38#73598562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90765467-C-A

73598562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765467-C-G

73598572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765487-G-A

73598758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765693-T-A

73598758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90765693-T-C

73599571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, undefined
orthologous variants: 90766193-C-G

73599846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90766375-A-G

73599869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90766399-C-G

73599988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90766503-G-T

73600012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90766525-G-A

73600179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767371-A-G

73600209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767403-T-G

73600279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767472-G-A

73600383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767572-T-A

73600569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767743-T-C

73600612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767790-A-G

73600655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90767830-C-T

73600886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768053-A-G

http://identifiers.org/hco/4/GRCh38#73601124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90768240-C-A

73601162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768272-A-G

73601788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768411-G-T

73601946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768587-T-C

http://identifiers.org/hco/4/GRCh38#73601998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90768626-C-A

73602075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768686-T-C

73602167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768749-G-A

73602232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768802-C-T

http://identifiers.org/hco/4/GRCh38#73602295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90768864-A-C

73602300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768869-G-A

73602300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90768869-G-C

73602487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769024-C-T

73602553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769079-G-C

73602596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769108-C-T

73602599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769111-G-A

73602675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769178-G-A

73603121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769338-T-G

73603199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769410-G-A

73603359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769573-T-C

73603578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, undefined
orthologous variants: 90769796-A-G

73603613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769830-A-G

73603623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769840-G-A

73603705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90769908-A-G

73603851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90770055-T-A

73603851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron variant
orthologous variants: 90770055-T-C

http://identifiers.org/hco/4/GRCh38#73604627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90770442-C-A

73604704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770522-A-G

73605185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770890-C-T

73606577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90772809-T-C

73606728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90772976-G-A

73606734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90772982-T-A

73606747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90772995-G-A

73606747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90772995-G-T

73606777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773019-T-C

73606882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90773136-T-A

73606883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90773137-C-T

73606888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90773142-C-T

73606981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773220-G-A

73607007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90773243-T-G

73607067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773290-A-G

73607067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773290-A-T

73607076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773298-T-C

73607100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773329-C-T

73607106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773335-G-A

73607106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773335-G-C

73607165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773371-T-C

73607259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773461-G-A

73607297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773500-A-G

73607299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773502-C-T

73607318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90773521-T-A

http://identifiers.org/hco/4/GRCh38#73607778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90774063-C-A

73607778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774063-C-G

73608092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774146-G-A

73608137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774191-A-G

73608184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774293-T-C

73608184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774293-T-G

73608230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774339-C-G

73608636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90774744-G-T

73608973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775088-T-A

73609373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775449-C-G

73609519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775586-C-T

73609639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775732-T-C

73609648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775741-C-T

73609685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775775-C-T

73609792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90775878-C-T

73609972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90776049-A-G

73609990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90776066-T-A

73610545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90778136-A-G

73610604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90778197-G-A

73611357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90778896-A-G

73611525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779114-T-A

73611578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779146-G-A

http://identifiers.org/hco/4/GRCh38#73611592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90779160-C-A

73611592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779160-C-T

73611614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779180-A-G

73611673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779239-G-A

73611673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90779239-G-T

73611678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779244-T-C

73611721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779357-G-T

73611847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779484-A-G

73611847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779484-A-T

73611901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779538-G-A

73611901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779538-G-T

73611922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779559-G-T

73612245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779701-T-C

73612345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779801-A-G

73612432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779885-A-T

73612496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779939-A-T

73612562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779991-G-A

73612562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90779991-G-T

73612628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780052-G-C

73612939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780704-T-C

73612972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780737-A-T

73613006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780769-A-G

73613024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780780-C-G

73613024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90780780-C-T

73613578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781295-T-C

73613602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781319-C-T

http://identifiers.org/hco/4/GRCh38#73613910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90781604-C-A

73613910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781604-C-T

73613911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781605-G-A

73613911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781605-G-T

73613915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781609-C-G

73614075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781770-A-G

73614490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90781908-C-G

73614644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782053-C-T

73614658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782065-A-G

73614851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782217-C-G

73614853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782219-G-A

73615268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782399-C-T

http://identifiers.org/hco/4/GRCh38#73615285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90782413-C-A

73615285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782413-C-G

73615599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782739-G-T

73615642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90782783-T-C

73615782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90782916-A-G

http://identifiers.org/hco/4/GRCh38#73615794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90782928-C-A

73615794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90782928-C-T

73615822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90782956-A-G

73615835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90782994-G-T

http://identifiers.org/hco/4/GRCh38#73615842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90783001-C-A

73615842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783001-C-T

73615846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783005-C-T

73615850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783009-G-A

73615850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783009-G-T

73615892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 90783051-A-G

73615925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783083-A-G

73615957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783115-T-C

73615961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783119-T-C

http://identifiers.org/hco/4/GRCh38#73615962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90783120-C-A

73615962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783120-C-G

73615962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783120-C-T

73615979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783133-T-C

73615981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783135-C-T

73615985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90783138-T-A

73616350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90783396-T-A

73616665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90783684-C-G

73616665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90783684-C-T

73616675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90783696-A-G

73617077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784111-T-C

73617237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784284-A-T

73617256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784292-T-C

73617313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784341-A-G

73617376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784403-T-G

73617441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784445-A-G

73617463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784461-G-A

73617494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784492-C-T

73617541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784540-G-A

73617545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784544-C-T

73617715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784702-G-A

73617715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784702-G-T

73617781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90784736-A-G

73617950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786297-C-T

73618139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786469-C-T

73618367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786613-T-C

73618498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786739-T-C

73618579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786800-T-C

73618618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786831-C-T

73618662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90786875-G-A

73618921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787036-A-G

73618993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787108-G-A

73619060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787163-T-A

73619152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787255-C-G

73619341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787429-C-T

73619399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787470-C-G

73619503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787577-T-C

73619677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787757-C-G

http://identifiers.org/hco/4/GRCh38#73619693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90787773-C-A

73619693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787773-C-T

73619725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787804-G-C

73619789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787862-C-T

73619809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787882-G-C

73619809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90787882-G-T

73620047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788052-C-T

73620083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788076-T-C

73620237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788228-T-C

73620257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788271-G-T

73620267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788281-T-A

73620267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788281-T-C

73620273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90788287-A-G

73620294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788307-T-C

http://identifiers.org/hco/4/GRCh38#73620325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90788337-C-A

73620325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788337-C-G

73620325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788337-C-T

73620383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788377-G-A

73620383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788377-G-T

73620405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788401-T-C

73620413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788409-G-A

73620413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90788409-G-T

73620501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788499-G-A

73620501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788499-G-C

73620501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788499-G-T

http://identifiers.org/hco/4/GRCh38#73620503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90788501-C-A

73620503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788501-C-T

73620578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788548-T-C

73620578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20796
most severe consequence: 5 prime UTR variant
orthologous variants: 90788548-T-G