72281035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89822784-T-C

72281348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89823098-G-A

72281348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89823098-G-T

http://identifiers.org/hco/4/GRCh38#72281958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89824010-C-A

72282243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824250-T-C

72282248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824255-G-A

72282248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824255-G-T

72282318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824314-G-A

72282318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824314-G-T

72282320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824316-T-A

72282320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824316-T-C

http://identifiers.org/hco/4/GRCh38#72282321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89824317-C-A

72282341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824337-T-A

72282650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824616-A-G

http://identifiers.org/hco/4/GRCh38#72282875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89824913-C-A

72282875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89824913-C-T

72282942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89825027-G-A

72282942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89825027-G-C

72282942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89825027-G-T

72283017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 3 prime UTR variant
orthologous variants: 89825102-T-G

72283200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89825290-G-A

http://identifiers.org/hco/4/GRCh38#72283352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89825436-A-C

72283352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89825436-A-G

http://identifiers.org/hco/4/GRCh38#72283361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89825445-C-A

72283364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89825448-G-A

72283416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89825497-T-C

72283577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89825658-T-C

72283580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89825661-T-C

72283688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89825769-T-C

72283732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89825813-A-G

72283754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89825827-T-A

72283785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89825852-G-C

72283785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89825852-G-T

72283905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826215-T-C

72283965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826276-T-G

http://identifiers.org/hco/4/GRCh38#72283985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89826302-C-A

72284031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826338-G-T

72284064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826367-A-G

72284131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826436-C-G

http://identifiers.org/hco/4/GRCh38#72284464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89826721-C-A

72284464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826721-C-T

72284468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89826725-A-T

72285226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827125-T-C

72285254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827148-G-A

72285295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827187-T-A

72285568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827430-A-T

72285627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827480-T-C

72285768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827591-G-A

72285768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827591-G-C

72285768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827591-G-T

http://identifiers.org/hco/4/GRCh38#72285875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89827661-A-C

72285876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827662-C-G

72285876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89827662-C-T

72288613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89830869-A-G

http://identifiers.org/hco/4/GRCh38#72288697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89830947-C-A

72288697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89830947-C-T

72288731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89830981-T-C

http://identifiers.org/hco/4/GRCh38#72288732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89830982-C-A

72288740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89830990-G-A

72288740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89830990-G-T

http://identifiers.org/hco/4/GRCh38#72288909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89831159-C-A

72288909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831159-C-T

http://identifiers.org/hco/4/GRCh38#72288914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89831164-C-A

72288914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831164-C-G

http://identifiers.org/hco/4/GRCh38#72288926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89831176-A-C

72288926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831176-A-G

72288926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831176-A-T

http://identifiers.org/hco/4/GRCh38#72288963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89831210-C-A

72288963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831210-C-G

72288963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831210-C-T

72288966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831213-A-T

72289011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831262-G-A

72290103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831565-C-T

72290309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831747-C-G

72290332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831770-A-G

72290332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89831770-A-T

72290671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89832084-T-C

72290882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89832198-T-C

72290896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89832212-C-T

72290996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89832312-A-G

72290996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89832312-A-T

72291041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89832357-T-A

72291041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89832357-T-C

72291041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89832357-T-G

72292602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89832777-A-G

72295302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834309-T-C

72295345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834342-T-G

http://identifiers.org/hco/4/GRCh38#72295369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89834375-A-C

72295474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834476-A-G

72295515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834516-A-G

72295812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834788-G-A

72295812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89834788-G-T

72296094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89835078-T-C

72296135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89835118-C-T

72296137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89835119-C-T

http://identifiers.org/hco/4/GRCh38#72296285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89835270-C-A

72296285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89835270-C-T

72296402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835382-C-T

72296446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835397-T-C

72296542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835508-G-T

72296655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835585-C-T

72297031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835898-A-G

72297075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835941-G-A

72297084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89835951-C-T

72297365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836203-T-C

72297636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836479-G-C

72297654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836497-G-A

72297711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836656-C-T

72297762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836748-G-C

http://identifiers.org/hco/4/GRCh38#72297775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89836762-C-A

72297794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836781-G-C

72297851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836837-A-G

72297925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836913-A-G

72298009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89836986-G-A

72298293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89839175-G-A

http://identifiers.org/hco/4/GRCh38#72298425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89839307-A-C

http://identifiers.org/hco/4/GRCh38#72298510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89839389-A-C

72298518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89839397-G-C

http://identifiers.org/hco/4/GRCh38#72298549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89839430-C-A

72298549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89839430-C-G

72298549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89839430-C-T

72298571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89839446-T-A

72303767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89840760-T-A

72303767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89840760-T-G

72303894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89840879-C-G

http://identifiers.org/hco/4/GRCh38#72304145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89841121-A-C

72304153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89841129-T-A

http://identifiers.org/hco/4/GRCh38#72304205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89841188-C-A

http://identifiers.org/hco/4/GRCh38#72304255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89841238-C-A

72304256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89841239-A-G

72304256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89841239-A-T

72304304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89841284-T-C

http://identifiers.org/hco/4/GRCh38#72304580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89841501-A-C

72305162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842008-C-T

72305163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842009-T-C

72305222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842068-T-C

72305322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842136-A-G

72305521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842304-G-A

72305847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842482-T-C

72305849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842484-C-T

http://identifiers.org/hco/4/GRCh38#72305855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89842490-C-A

72305855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842490-C-G

72305855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842490-C-T

72305864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842499-A-G

72305866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842501-G-A

72305866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842501-G-T

72305873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842508-C-T

http://identifiers.org/hco/4/GRCh38#72305970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89842592-C-A

72305970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842592-C-T

72306093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842715-G-A

http://identifiers.org/hco/4/GRCh38#72306153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89842773-C-A

72306437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89842983-G-C

72306703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843170-G-A

72307053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843493-A-G

72307218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843644-C-T

72307242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843668-T-G

72307259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89843684-G-A

72307635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844088-A-G

72307893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844348-T-C

72308353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89844862-G-A

http://identifiers.org/hco/4/GRCh38#72308514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89845135-C-A

72308514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845135-C-T

72308515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845136-G-A

72308544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845269-G-A

72308629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845352-T-C

72308744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845444-T-C

72309027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845762-C-T

72309247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89845940-A-T

72309349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846016-T-A

72309443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89846109-G-A

http://identifiers.org/hco/4/GRCh38#72309538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89846204-C-A

72309538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846204-C-T

72309542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846208-T-C

72309544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846210-T-C

http://identifiers.org/hco/4/GRCh38#72309608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89846267-C-A

72309611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846270-G-A

72309611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846270-G-T

http://identifiers.org/hco/4/GRCh38#72309645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89846280-C-A

72309645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846280-C-T

72309880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846526-T-C

72310137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846786-A-G

72310156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846805-C-T

72310193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846842-C-T

72310306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89846939-G-A

72310505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89847598-A-G

72310508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89847601-G-A

72310609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89847694-A-G

72311015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89848233-T-C

72311096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89848314-G-A

72311325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89848536-T-A

72311981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89849207-A-G

72312008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89849233-T-C

http://identifiers.org/hco/4/GRCh38#72312021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849246-C-A

72312021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89849246-C-T

http://identifiers.org/hco/4/GRCh38#72312034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849260-C-A

72312066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89849265-T-C

72312073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89849272-G-T

http://identifiers.org/hco/4/GRCh38#72312111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849314-C-A

http://identifiers.org/hco/4/GRCh38#72312194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849398-C-A

72312194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89849398-C-G

http://identifiers.org/hco/4/GRCh38#72312195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849399-C-A

72312202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89849410-G-C

72312203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89849411-G-T

72312224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89849432-G-A

72312224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89849432-G-C

72312224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89849432-G-T

http://identifiers.org/hco/4/GRCh38#72312278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849486-C-A

72312278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89849486-C-T

72312551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89849757-G-T

72312578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89849783-A-G

http://identifiers.org/hco/4/GRCh38#72312590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849795-C-A

72312590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89849795-C-G

http://identifiers.org/hco/4/GRCh38#72312597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849802-C-A

72312597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89849802-C-T

http://identifiers.org/hco/4/GRCh38#72312617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89849822-A-C

72312617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89849822-A-G

72312625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89849831-C-G

72312774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89849958-T-A

72312919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850099-C-T

72312952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850133-G-A

72313017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850189-G-T

72313022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850193-T-C

72313096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850264-C-T

72313183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850335-G-A

72313335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850478-T-C

http://identifiers.org/hco/4/GRCh38#72313584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89850699-A-C

72313584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850699-A-G

72313584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850699-A-T

http://identifiers.org/hco/4/GRCh38#72313715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89850831-A-C

72313715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89850831-A-G

72313715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89850831-A-T

72313724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89850840-T-A

72313724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89850840-T-C

72313834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850950-G-A

72313834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89850950-G-T

http://identifiers.org/hco/4/GRCh38#72313964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89851060-C-A

72313964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851060-C-G

72314003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851099-G-T

72314130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851435-T-C

72314137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851442-T-C

72314353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851643-T-C

72314387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851678-G-A

72314547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851852-C-T

72314550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851855-C-T

72314551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89851856-G-A

http://identifiers.org/hco/4/GRCh38#72314965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89852245-C-A

http://identifiers.org/hco/4/GRCh38#72315176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89852457-A-C

72315307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852593-C-T

72315315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852601-A-T

http://identifiers.org/hco/4/GRCh38#72315495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89852768-A-C

72315503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852782-G-A

72315546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852789-T-C

72315708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852925-A-G

72315748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852965-T-A

72315748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852965-T-C

72315761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89852971-A-T

72315813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853009-A-T

72315815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853011-G-T

http://identifiers.org/hco/4/GRCh38#72315819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89853015-C-A

72315819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853015-C-T

72315836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853027-T-C

72315954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous_variant, undefined
orthologous variants: 89853146-T-C

72315954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous_variant, undefined
orthologous variants: 89853146-T-G

72315992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853184-T-C

72315993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853185-T-C

72315993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853185-T-G

72316011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853203-T-C

http://identifiers.org/hco/4/GRCh38#72316043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89853235-C-A

72316043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853235-C-G

http://identifiers.org/hco/4/GRCh38#72316044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89853236-A-C

72316046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853238-T-A

72316097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89853317-T-C

http://identifiers.org/hco/4/GRCh38#72318421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89854361-C-A

http://identifiers.org/hco/4/GRCh38#72318451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89854389-A-C

72318467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854404-T-C

72318467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854404-T-G

http://identifiers.org/hco/4/GRCh38#72318568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89854505-A-C

72318568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854505-A-G

72318595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89854532-C-T

72318641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89854578-A-T

72318665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89854602-A-G

http://identifiers.org/hco/4/GRCh38#72318668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89854605-A-C

72318668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89854605-A-G

72318668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89854605-A-T

72318756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854686-T-C

72318756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854686-T-G

72318787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854718-T-A

72318787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854718-T-C

http://identifiers.org/hco/4/GRCh38#72318821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89854750-C-A

72318821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854750-C-T

72318911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854833-A-G

72318917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854839-G-C

72318917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854839-G-T

72318940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854862-C-G

72318940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854862-C-T

72318941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854863-G-A

72319005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89854916-G-T

72319087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855005-G-A

72319095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855008-T-G

http://identifiers.org/hco/4/GRCh38#72319188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855099-C-A

72319188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855099-C-T

72319201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855112-G-A

72319201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855112-G-T

72319315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855147-T-C

72319427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855259-A-G

72319427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855259-A-T

72319436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855268-A-G

http://identifiers.org/hco/4/GRCh38#72319457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855289-A-C

72319457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855289-A-G

72319482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89855314-C-T

http://identifiers.org/hco/4/GRCh38#72319484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855316-C-A

72319532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855365-T-A

72319564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855393-G-A

72319564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855393-G-C

72319564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855393-G-T

http://identifiers.org/hco/4/GRCh38#72319620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855452-C-A

72319620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855452-C-T

http://identifiers.org/hco/4/GRCh38#72319621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855453-A-C

72319662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855498-C-T

72319669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855505-A-G

http://identifiers.org/hco/4/GRCh38#72319744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855580-C-A

72319744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855580-C-T

72319759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855594-G-T

72319785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855621-G-A

72319785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855621-G-T

72319847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89855650-C-T

72319947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855750-G-A

72319950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89855753-G-A

http://identifiers.org/hco/4/GRCh38#72319983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855786-C-A

72319983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855786-C-G

72320008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855841-C-T

http://identifiers.org/hco/4/GRCh38#72320059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855892-C-A

72320059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855892-C-G

72320061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855894-T-C

http://identifiers.org/hco/4/GRCh38#72320080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89855913-A-C

72320225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89855995-G-A

72320478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856218-C-G

72320478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856218-C-T

72320595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856354-G-T

72320605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856365-G-A

72320605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856365-G-T

http://identifiers.org/hco/4/GRCh38#72320615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89856375-A-C

72320615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856375-A-T

72320625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856384-A-G

72320775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89856531-A-G

72320778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89856534-G-T

72320922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856654-C-T

72320923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856655-G-A

72320923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856655-G-C

72320923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856655-G-T

http://identifiers.org/hco/4/GRCh38#72321524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89856875-C-A

72321554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89856906-A-G

72322017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89857399-A-G

http://identifiers.org/hco/4/GRCh38#72322184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89857561-C-A

72322226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89857628-T-C

72322286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89857691-G-A

72322485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89857902-T-C

72322512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89857927-C-T

72322702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89858095-C-G

72323193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858702-T-A

72323193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858702-T-C

72323216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858727-T-C

72323223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858732-G-C

72323223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858732-G-T

72323273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858782-G-A

72323273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858782-G-T

72323335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858843-A-G

72323397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858931-C-T

72323415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89858951-A-G

72323524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859050-G-C

72323528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859054-C-G

72323952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859481-G-A

72324053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859603-G-T

72324112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859665-C-T

72324282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859816-T-G

72324402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859932-C-G

72324402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859932-C-T

http://identifiers.org/hco/4/GRCh38#72324700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89860223-C-A

72324903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89860417-A-G

72326153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89861875-T-C

http://identifiers.org/hco/4/GRCh38#72326286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89862010-A-C

72326286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862010-A-G

72326299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862024-G-T

72326433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862161-T-C

72326466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862189-T-C

72326472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862195-T-C

72326491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862214-G-A

72326522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862244-G-A

72326574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862300-A-G

72326586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862312-C-T

72326640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862368-T-C

72326682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862406-T-C

72326684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862408-C-T

72326755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862439-T-C

72326919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862628-G-A

72327147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89862849-C-T

72327352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863029-G-T

72327991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863425-G-A

72327999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863433-T-C

72328343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863753-G-A

http://identifiers.org/hco/4/GRCh38#72328685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89864087-C-A

72328721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89864122-C-T

72328723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89864124-A-G

72328846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89864222-G-T

72328954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89864319-T-C

72329092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89864464-T-C

72331726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89865396-T-G

72331875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89865532-T-C

72332068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89865714-G-T

http://identifiers.org/hco/4/GRCh38#72332194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89865838-A-C

72332329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89865948-T-C

72338487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868563-A-T

72338594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868681-G-A

72338709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868766-G-A

72338734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868791-A-G

72338734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868791-A-T

72338742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89868799-A-T

72339198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869229-A-G

http://identifiers.org/hco/4/GRCh38#72339378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89869406-C-A

72339378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869406-C-T

http://identifiers.org/hco/4/GRCh38#72339396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89869424-C-A

72339396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869424-C-T

http://identifiers.org/hco/4/GRCh38#72339410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89869430-C-A

72339718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869738-G-A

72339718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869738-G-C

http://identifiers.org/hco/4/GRCh38#72339838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89869856-A-C

72339838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869856-A-G

http://identifiers.org/hco/4/GRCh38#72339861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89869879-C-A

72339861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869879-C-G

72339861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89869879-C-T

72340954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89870763-G-A

72341360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89871161-A-G

72341623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89871420-C-T

72341685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89871475-G-A

72341879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89871658-G-A

72344278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875177-T-A

72344327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875227-C-T

72344498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875384-A-G

http://identifiers.org/hco/4/GRCh38#72344560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89875443-C-A

72344636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875519-T-A

72344659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875582-G-C

72344677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875600-G-A

72344854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875742-C-T

72344920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875805-T-G

72345020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89875902-T-C

72345154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89876043-T-C

72345352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89876242-G-A

72345352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89876242-G-C

72345794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89876668-G-A

72346226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89877111-T-C

72346537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89877543-C-G

http://identifiers.org/hco/4/GRCh38#72346690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89877695-C-A

http://identifiers.org/hco/4/GRCh38#72346828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89877827-A-C

72347233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89877880-T-C

72347263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89877907-A-T

http://identifiers.org/hco/4/GRCh38#72347303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89877927-C-A

72347303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89877927-C-T

72347517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878112-G-A

72347549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878139-G-T

72347585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878177-C-T

72347748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878342-T-C

72347973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878547-G-A

72348092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878653-C-G

72348208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878763-C-T

72348280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878834-G-A

72348392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89878946-T-C

72350462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89880647-T-C

72350547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89880733-T-A

72350689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89880871-C-T

72350715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89880897-G-A

72350850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89880998-T-C

72350951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881093-C-G

72350991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881127-T-C

72351060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881200-A-G

72351074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881214-G-A

72351133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881282-C-T

72351395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881532-G-A

72351404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881541-T-C

72351681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881776-G-A

http://identifiers.org/hco/4/GRCh38#72351761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89881859-C-A

72351818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881910-G-C

72351856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881940-T-C

72351879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89881963-G-A

http://identifiers.org/hco/4/GRCh38#72351938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89882015-C-A

72351938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89882015-C-T

72352124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89882182-A-T

72353987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89882973-T-C

72353987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89882973-T-G

72354267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883230-C-G

72354398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883421-A-G

72354502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883508-G-A

72354540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883548-T-G

72354667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883661-T-C

72354705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883687-A-G

72355008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89883964-C-G

72355054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89884010-C-T

72365074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89885901-C-T

72365079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89885907-A-G

72365249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89886100-T-C

72365312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89886158-T-C

72365313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89886159-G-A

72365583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89888768-T-C

72366092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89889240-G-A

72366156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89889277-T-C

72366340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89889392-T-C

72366436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89889493-G-T

72374095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89895222-T-G

72374285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89895614-A-T

72374358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89895682-C-G

72374358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89895682-C-T

72374932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89896271-T-C

72374941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89896280-T-C

72374954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89896293-T-C

72375175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89896528-C-T

72375188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89896541-C-T

72375220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89896566-T-C

http://identifiers.org/hco/4/GRCh38#72375650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89896984-A-C

72375650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89896984-A-G

72375718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897052-A-G

http://identifiers.org/hco/4/GRCh38#72375946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89897267-C-A

http://identifiers.org/hco/4/GRCh38#72375995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89897313-C-A

72376095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897462-G-A

72376172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897537-C-T

72376185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897549-A-G

72376241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897603-G-A

72376327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89897694-G-T

72378477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900286-G-T

72378525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900316-C-T

72378604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900405-T-A

72378930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900706-G-A

http://identifiers.org/hco/4/GRCh38#72378974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89900753-A-C

72378985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900764-A-G

72379228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89900979-T-C

72379415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901170-T-G

72379433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901186-G-A

72379433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901186-G-T

http://identifiers.org/hco/4/GRCh38#72379628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89901363-A-C

72379628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901363-A-G

72379657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901392-T-C

72379867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89901551-T-G

72380387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89902050-C-T

72380447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89902110-A-G

72380470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89902131-A-G

72383366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89903328-C-T

http://identifiers.org/hco/4/GRCh38#72383416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89903377-A-C

72385984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89905593-T-C

72386003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89905613-T-G

72386181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89905844-C-T

72386588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89906253-G-A

72386712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89906390-A-G

72386772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89906429-C-T

72386853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89906500-G-A

72387003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89906641-A-T

72387523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907260-C-T

72387605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907331-T-C

72387606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907332-G-A

72387627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907353-A-G

72387761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907484-G-A

72387767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89907490-G-A

72392216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89909891-C-T

72392226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89909901-A-T

72392428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910133-C-T

72392471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910171-T-C

http://identifiers.org/hco/4/GRCh38#72392538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89910238-C-A

72392805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910435-G-C

72392887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910532-G-A

72393442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910939-G-T

72393520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89910990-C-G

72393531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89911001-G-A

72393531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89911001-G-T

72393646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89911102-A-G

http://identifiers.org/hco/4/GRCh38#72394547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89911954-C-A

72394650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89912057-G-A

72394693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89912104-C-T

72395701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89913559-A-T

72401733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89914455-A-G

72402344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89915029-G-A

72402847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89915494-G-A

72403142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89915782-G-T

http://identifiers.org/hco/4/GRCh38#72403166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89915806-C-A

72406950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89917422-C-T

72407306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89917782-T-C

72407310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89917786-A-G

72409701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89918144-T-C

72409759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89918210-G-T

72410030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89918473-A-T

http://identifiers.org/hco/4/GRCh38#72410247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89918677-C-A

72410570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89918990-T-C

http://identifiers.org/hco/4/GRCh38#72410877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89919306-C-A

72411676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89919855-G-T

72411858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89920010-C-T

72413130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89922626-G-A

72413130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89922626-G-C

72414807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89923136-A-G

72414807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 89923136-A-T

http://identifiers.org/hco/4/GRCh38#72414827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89923156-A-C

72414827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89923156-A-G

72414827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89923156-A-T

72414828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89923157-G-A

http://identifiers.org/hco/4/GRCh38#72414851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89923180-C-A

72414851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89923180-C-T

http://identifiers.org/hco/4/GRCh38#72414852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89923181-C-A

72414852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: synonymous variant
orthologous variants: 89923181-C-T

72414853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89923182-T-C

72414881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense variant
orthologous variants: 89923210-C-T

72417426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89925059-T-C

72417427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89925060-G-A

72417538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89925169-G-C

72418034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89926177-C-T

72418042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89926186-T-C

72418072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89926208-T-C

72418188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89926304-T-C

72418651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89926685-T-C

http://identifiers.org/hco/4/GRCh38#72418708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89926742-C-A

72418708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: 89926742-C-G

http://identifiers.org/hco/4/GRCh38#72418823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#89926845-C-A

72419111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89927046-T-C

http://identifiers.org/hco/4/GRCh38#72419113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89927048-C-A

72419220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89927143-T-A

72419336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89927259-G-T

72419435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89927426-G-C

72420122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89927849-G-A

72420448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89928119-C-T

72420556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89928218-C-T

72420628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89928313-T-C

72421000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89928735-G-A

72421000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89928735-G-C

http://identifiers.org/hco/4/GRCh38#72421377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89928972-A-C

72421492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929067-T-C

72421550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929125-G-A

http://identifiers.org/hco/4/GRCh38#72421770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89929314-C-A

http://identifiers.org/hco/4/GRCh38#72422001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89929566-C-A

72422049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929616-T-A

72422216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929804-T-A

72422221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929809-G-A

72422255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929837-T-G

72422380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89929920-A-G

http://identifiers.org/hco/4/GRCh38#72422527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89930056-C-A

72422539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89930068-G-T

72422841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89930346-A-G

72423427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89930881-T-C

72423983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931246-T-C

72424228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931358-G-A

72424480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931577-A-G

72424570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931652-C-T

72424629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931715-T-C

72424881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89931949-T-C

72424908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89932030-T-C

72424949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89932126-T-C

72424950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89932127-A-G

72427275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89932902-C-T

72427478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89933072-T-C

72427761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89934543-T-C

http://identifiers.org/hco/4/GRCh38#72428018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89934746-A-C

72428034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89934762-C-G

72428076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89934801-T-C

http://identifiers.org/hco/4/GRCh38#72428077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89934802-C-A

72428131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89934839-G-C

72428660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89935402-G-T

72428679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89935421-G-T

http://identifiers.org/hco/4/GRCh38#72428989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89935731-C-A

72429098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89935839-T-A

72429098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89935839-T-C

72429143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89935883-T-C

http://identifiers.org/hco/4/GRCh38#72429151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89935891-C-A

http://identifiers.org/hco/4/GRCh38#72429165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89935904-C-A

72429308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89936105-A-G

72429421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89936217-C-T

72432929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89937955-C-G

72432929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89937955-C-T

72433321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89938253-T-A

http://identifiers.org/hco/4/GRCh38#72433588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89938914-C-A

72433634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89938960-T-C

72437146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89940376-T-C

72437871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89941113-G-A

72438882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89941306-T-C

72438911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89941336-T-C

72439656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942069-C-T

72439888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942474-T-C

72439894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942480-C-T

72440023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942780-C-T

http://identifiers.org/hco/4/GRCh38#72440077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89942836-C-A

72440097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942856-C-T

72440105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942864-A-T

72440179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942927-T-C

72440229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89942977-G-C

72440269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943014-A-G

72440311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943051-G-A

72440450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943162-T-C

72440460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943172-A-T

72440480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943190-G-A

72440489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943199-A-G

72440613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943312-C-T

72440641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943340-T-A

72440641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943340-T-C

72441196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron variant
orthologous variants: 89943826-A-G

72443272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89944374-C-T

72443457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89944675-A-G

72443616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89944832-T-C

72443634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89944851-T-C

72443781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89945196-T-G

72443792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89945207-C-T

72443795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89945210-G-A

http://identifiers.org/hco/4/GRCh38#72444129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89945520-C-A

72444129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89945520-C-G

72444409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89945774-G-C

72446403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946189-C-T

72446481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946258-A-G

72446506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946284-C-T

72446528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946306-G-A

72446964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946678-C-T

72447100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89946816-A-G

http://identifiers.org/hco/4/GRCh38#72447213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89946926-A-C

72447531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947226-T-C

72447674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947360-T-C

72447675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947361-C-T

72447686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947372-G-C

72447797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947451-A-G

72450708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947704-C-T

72450720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947716-A-G

72450724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947720-T-A

72450799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947774-C-G

72450842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947822-T-C

72450903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89947867-G-A

72451140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89948106-T-C

72451683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89948643-C-G

http://identifiers.org/hco/4/GRCh38#72452176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89948831-A-C

72452360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89949001-C-G

72452426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89949063-A-G

72454353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955073-A-T

72454654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955411-A-T

72454733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955487-C-G

72454974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955713-T-G

72455005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955747-G-C

72455013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955762-G-C

72455013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89955762-G-T

72456777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89956838-G-A

72456781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89956839-G-A

72456864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89956920-C-T

72458350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89957457-C-T

72458385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89957505-G-C

72458560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89957684-G-A

72458560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89957684-G-C

72458593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89957717-T-A

72460203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961486-C-T

72460219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961502-T-C

72460436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961698-A-G

http://identifiers.org/hco/4/GRCh38#72460442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89961704-C-A

72460442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961704-C-T

72460491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961748-G-T

http://identifiers.org/hco/4/GRCh38#72460501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89961758-A-C

http://identifiers.org/hco/4/GRCh38#72460613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89961862-C-A

72460615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89961864-T-C

72460867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962112-T-A

72460964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962204-G-A

72460979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962219-A-G

72460997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962237-A-T

72461032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962275-A-G

72461032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962275-A-T

72461227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962416-G-C

72461316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89962498-T-C

72463359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89963909-T-A

72463663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89964174-A-T

72463674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89964185-A-T

72463692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89964203-A-T

http://identifiers.org/hco/4/GRCh38#72463718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89964236-C-A

72463718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89964236-C-G

72463718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89964236-C-T

http://identifiers.org/hco/4/GRCh38#72464535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89965054-A-C

72464537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965056-T-C

72464724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965226-G-A

72464788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965296-T-C

72464851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965362-G-A

72465092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965569-T-C

72465148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89965626-T-C

http://identifiers.org/hco/4/GRCh38#72465333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89965788-A-C

72467016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89966622-A-G

72467162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89966748-T-A

72468381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89966943-T-C

72468710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89967234-A-T

http://identifiers.org/hco/4/GRCh38#72468942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89967437-A-C

72469035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89967525-C-T

72469041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89967531-T-C

72469276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89968810-T-G

72469367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89968858-G-A

72469562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89969047-T-C

72471743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970080-T-C

72472053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970386-G-C

72472163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970492-A-G

72472329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970656-C-G

72472412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970738-T-C

72472470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89970790-C-T

http://identifiers.org/hco/4/GRCh38#72472546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89970864-A-C

http://identifiers.org/hco/4/GRCh38#72472737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89971111-A-C

72472737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89971111-A-T

72472824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89971199-G-A

72483176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979200-G-A

72483215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979223-C-T

72483364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979338-T-C

72483386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979359-C-T

72483495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979488-G-C

72483496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979489-T-G

72483544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979537-C-G

72483597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979588-A-G

72483620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979613-C-G

72483722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89979703-A-G

http://identifiers.org/hco/4/GRCh38#72496143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89981455-C-A

72496375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89981611-T-C

72496405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89981640-G-A

72496417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89981652-C-T

72496437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89981663-T-A

72496519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89981743-G-A

72496536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89981764-T-C

http://identifiers.org/hco/4/GRCh38#72496846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89982051-C-A

72496867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89982073-C-T

72498324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89982748-T-C

72498335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89982759-G-A

72498381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89982804-A-G

72498495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89983038-T-C

72498668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89983177-C-T

72498671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89983180-A-G

72498673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89983182-A-G

http://identifiers.org/hco/4/GRCh38#72498992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89983421-A-C

72499209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89984094-A-G

72514074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89985273-C-T

72514482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89985652-G-A

72514534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89985703-T-C

72514553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89985717-T-A

72514642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89985786-T-C

72521582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89986141-T-A

72521674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89986230-C-T

72522636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89987163-T-A

http://identifiers.org/hco/4/GRCh38#72522823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89987353-A-C

72522856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89987386-A-G

72522869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89987390-A-T

http://identifiers.org/hco/4/GRCh38#72522953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89987465-C-A

72523389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989425-C-T

72523394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989430-T-C

72523412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989448-T-G

72523761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989781-C-T

72523774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989794-G-T

72523847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89989870-A-G

72524198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990312-G-T

72524219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990333-A-G

72524340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990434-G-C

72524340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990434-G-T

72524429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990503-T-C

72524886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89990910-C-T

72525010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89991040-A-T

72525062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89991080-T-C

72525885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89992150-G-A

72525922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89992187-T-G

72526231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89992480-G-A

72526358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89992604-G-A

72526358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89992604-G-T

72526945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89993175-T-C

http://identifiers.org/hco/4/GRCh38#72526947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89993177-C-A

http://identifiers.org/hco/4/GRCh38#72527188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89993665-C-A

72527419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89993959-C-T

http://identifiers.org/hco/4/GRCh38#72527492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89994035-A-C

72527913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89994487-G-A

72528014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89994553-T-C

72528240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89994776-T-A

72528309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89994836-T-C

http://identifiers.org/hco/4/GRCh38#72528751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89995061-C-A

72529008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89995299-T-C

72529032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89995319-T-A

72529365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89995617-A-T

http://identifiers.org/hco/4/GRCh38#72529504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89995726-C-A

72531206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996097-T-C

72531315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996197-G-A

72531315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996197-G-C

72531494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996393-G-A

72531524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996424-G-C

72531699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996596-A-G

http://identifiers.org/hco/4/GRCh38#72531915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89996810-A-C

72531934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996829-G-A

72532025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996918-T-A

72532025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89996918-T-C

72532121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997536-T-C

72532177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997588-G-C

72532375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997763-C-T

72532458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997843-G-A

http://identifiers.org/hco/4/GRCh38#72533670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89997907-C-A

72533670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997907-C-G

72533670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997907-C-T

http://identifiers.org/hco/4/GRCh38#72533672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89997909-C-A

72533672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997909-C-G

72533672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997909-C-T

72533674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997911-T-A

72533676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997913-T-G

http://identifiers.org/hco/4/GRCh38#72533680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89997917-C-A

72533680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997917-C-G

72533680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997917-C-T

http://identifiers.org/hco/4/GRCh38#72533683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89997920-A-C

http://identifiers.org/hco/4/GRCh38#72533684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#89997921-C-A

72533684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997921-C-G

72533684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997921-C-T

72533688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997925-T-A

72533688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997925-T-C

72533688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997925-T-G

72533721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89997947-C-T

72533811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89998041-A-G

72533847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89998077-G-C

72534843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89998968-T-A

72534843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89998968-T-C

72534963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999015-C-G

72534963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999015-C-T

72534969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999021-T-C

72534978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999030-G-A

72535323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999377-C-T

72535328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999382-A-G

72535563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999587-A-G

72535563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89999587-A-T

72535769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90000196-T-C

72535911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90000519-T-G

72536079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90000674-A-G

72536236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90000854-T-C

72536400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90001018-G-A

72536414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90001032-A-G

72545329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007105-G-A

72545509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007256-G-A

72545517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007264-G-A

72545730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007445-G-A

72545781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007498-G-A

http://identifiers.org/hco/4/GRCh38#72545878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90007598-A-C

72546277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90007957-C-T

http://identifiers.org/hco/4/GRCh38#72546442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90008148-C-A

72546742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90008443-G-T

72546916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90008608-T-C

72547022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90008686-C-T

http://identifiers.org/hco/4/GRCh38#72547184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90008838-C-A

72547184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90008838-C-T

72548598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90009278-T-C

72548609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90009289-T-C

72548632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90009312-G-A

72548632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90009312-G-C

72548739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90009419-G-A

72548962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009626-C-T

72548988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009647-T-A

72548988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009647-T-C

72548988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009647-T-G

72548995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009654-T-C

72549023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009686-T-A

72549023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009686-T-C

72549023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009686-T-G

http://identifiers.org/hco/4/GRCh38#72549046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90009709-C-A

72549094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009746-T-C

72549310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90009934-G-A

72549455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010084-G-T

72549623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010286-T-A

72549800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010447-C-T

72550129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010588-G-T

72550193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010645-A-G

72550573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90010979-T-C

72550661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011053-C-G

72550709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011082-T-C

72550714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011087-A-G

72550793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011159-G-A

72551459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011787-C-T

72551538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011870-G-A

72551549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90011881-C-T

72551814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90012104-C-T

72552117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90012353-A-G

72552222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90012452-A-G

72552986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015539-C-G

72553015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015548-A-G

http://identifiers.org/hco/4/GRCh38#72553028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90015561-A-C

72553108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015632-T-C

http://identifiers.org/hco/4/GRCh38#72553148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90015671-C-A

72553148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015671-C-T

72553166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015689-G-A

72553166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015689-G-T

72553258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90015782-T-G

72553538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90016029-A-G

72553617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90016107-C-G

72553617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90016107-C-T

72553895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90016341-A-G

http://identifiers.org/hco/4/GRCh38#72553933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90016379-C-A

72554002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90016448-T-G

72554511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017357-T-C

72554511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017357-T-G

72554565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017395-T-G

72554666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017487-T-C

72554740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017563-G-C

72554758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017581-G-C

72554919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017753-G-T

72554923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017762-T-C

72554929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017768-T-A

72554947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017791-G-T

72555157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90017963-T-A

72556195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018452-G-A

http://identifiers.org/hco/4/GRCh38#72556249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90018486-C-A

72556493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018671-T-C

72556507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018685-A-G

72556598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018774-A-G

72556637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018813-G-A

72556753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018929-T-C

72556804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018962-C-G

72556804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018962-C-T

72556806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018964-T-C

72556853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90018990-T-C

72556919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019039-T-C

72556957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019077-C-G

72556957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019077-C-T

72557073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019192-T-C

72557108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019227-A-G

72557134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019256-T-C

72557225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019353-T-C

http://identifiers.org/hco/4/GRCh38#72557258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90019389-C-A

72557456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019574-T-C

72557471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019589-A-G

72557471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019589-A-T

72557497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90019613-T-C

72557990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020142-T-A

http://identifiers.org/hco/4/GRCh38#72558169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90020324-C-A

72558169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020324-C-G

72558169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020324-C-T

72558284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020487-G-A

72558313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020516-T-C

72558322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020524-C-T

72558340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020542-G-T

72558420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020643-T-A

72558637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90020837-A-G

72559087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90021058-G-A

72559397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90021552-T-G

72559409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90021564-C-T

72561871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90022437-G-A

72561873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90022439-G-A

72561973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90022538-G-A

72561973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90022538-G-C

72562544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023100-G-A

72562601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023197-T-C

72562602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023198-G-T

72562641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023290-T-A

72562810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023495-G-A

72562835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023525-G-A

72562998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023673-G-A

72563481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023903-T-C

72563495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90023917-C-T

72563602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90024010-T-G

72563821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90024226-T-C

72563914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90024297-G-A

72563994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90024403-G-C

72564189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90024567-C-T

72564685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90025032-G-C

72564706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90025045-G-T

72564883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90025229-T-C

72565382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026260-C-T

72565452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026315-G-A

72565614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026500-G-A

72565629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026512-G-A

72565629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026512-G-C

72565637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026520-C-T

72565938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90026832-A-G

72566652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90028696-C-T

72566940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90028975-G-A

72566940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90028975-G-T

72566959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90028994-C-T

72567178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029205-C-T

http://identifiers.org/hco/4/GRCh38#72567254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029277-C-A

72567255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029278-T-A

72567255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029278-T-C

http://identifiers.org/hco/4/GRCh38#72567257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029280-C-A

http://identifiers.org/hco/4/GRCh38#72567258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029281-A-C

72567258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029281-A-G

http://identifiers.org/hco/4/GRCh38#72567275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029294-C-A

72567275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029294-C-T

http://identifiers.org/hco/4/GRCh38#72567421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029443-C-A

72567462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029486-G-T

http://identifiers.org/hco/4/GRCh38#72567477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029500-C-A

72567477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029500-C-T

http://identifiers.org/hco/4/GRCh38#72567494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029517-A-C

72567528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029550-T-C

72567696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029728-T-C

72567715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029747-T-C

72567787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029815-C-T

72567824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90029850-G-A

http://identifiers.org/hco/4/GRCh38#72567927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90029952-C-A

72567927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90029952-C-T

72567930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90029955-T-A

72567995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90030019-G-A

72567995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90030019-G-T

http://identifiers.org/hco/4/GRCh38#72568090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90030117-C-A

72568090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030117-C-G

72568090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030117-C-T

72568092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030119-A-G

http://identifiers.org/hco/4/GRCh38#72568113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90030142-C-A

72568113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90030142-C-T

72568158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90030184-G-A

72568158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90030184-G-C

72568158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90030184-G-T

http://identifiers.org/hco/4/GRCh38#72568193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90030219-C-A

72568219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 90030245-C-T

72568287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030295-T-A

72568326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030314-G-A

72568388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030379-G-T

72568450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030441-G-A

72568469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030460-G-C

72568484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030477-G-A

72568595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030583-G-T

72568605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030595-G-A

72568605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 90030595-G-T

72568905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5 prime UTR variant
orthologous variants: 90030893-G-A

72568905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5 prime UTR variant
orthologous variants: 90030893-G-C

72568905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5 prime UTR variant
orthologous variants: 90030893-G-T

72569029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 90031014-G-A

72569029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 90031014-G-C

72569029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 90031014-G-T

http://identifiers.org/hco/4/GRCh38#72569075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 219
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90031056-C-A