111732520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773876-A-G

http://identifiers.org/hco/3/GRCh38#111732769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45773671-C-A

111732769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773671-C-T

111732793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-A

111732793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-C

111732793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-T

111732921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773517-G-A

111733076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773359-T-C

111733359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773126-T-G

111733384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773101-G-C

111733391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773094-C-G

111733391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773094-C-T

111733396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773086-C-G

111733622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772860-G-A

111733816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772683-A-G

111733825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772674-C-T

111733938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772558-G-A

111734083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772412-A-G

111734120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772376-T-C

http://identifiers.org/hco/3/GRCh38#111734124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45772372-A-C

111734124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772372-A-G

111734166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772344-G-T

111734218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772288-G-T

111734247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772259-G-A

111734247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772259-G-C

111734274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772245-T-C

http://identifiers.org/hco/3/GRCh38#111734567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45772129-A-C

111734567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772129-A-G

111734645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772062-G-T

111734680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772026-A-G

111734802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771891-A-G

111734982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771688-G-A

111735050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771632-T-C

111735099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771582-C-T

111735412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771069-A-G

111735485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770896-A-G

111735680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770701-C-G

111735695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770684-A-G

111735913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770467-G-C

111735937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770443-C-T

111735969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770411-A-G

111736016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770366-T-A

111736130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770256-C-T

111736157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770229-T-C

111736348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770058-G-A

111736521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769868-T-C

111736521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769868-T-G

111736619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769739-C-G

http://identifiers.org/hco/3/GRCh38#111736754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45769612-A-C

111736834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769539-T-G

111736876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769508-G-A

111737513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769226-C-T

111737780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768927-T-C

111737909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768799-A-G

111737961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768747-A-T

111738121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768591-G-A

http://identifiers.org/hco/3/GRCh38#111738167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45768554-A-C

111738376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768376-C-T

111738382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768370-G-A

111738563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768185-T-A

111738563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768185-T-G

111738620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768103-G-A

111739740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765553-G-A

http://identifiers.org/hco/3/GRCh38#111739827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45765457-C-A

111739829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765455-C-T

111740013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765275-A-G

111740042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765238-A-G

111740042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765238-A-T

111740065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45764177-C-T

111740493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763861-G-A

111740532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763823-C-T

111740606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763752-A-G

111741254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763362-C-T

http://identifiers.org/hco/3/GRCh38#111741293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45763330-C-A

111741386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763238-T-C

111741789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763123-T-A

111741837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763075-T-C

111742179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762743-C-G

111742954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762485-T-C

111743017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762428-G-A

111743102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762345-A-G

111743135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762312-G-C

111743260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762197-G-C

111743331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762102-G-A

http://identifiers.org/hco/3/GRCh38#111743382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45762051-A-C

111743455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761979-T-G

111743514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761924-G-T

111743535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761906-A-T

111743594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761850-A-G

111743629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761821-T-C

111743775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761674-T-C

111743803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761647-G-C

111744082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761364-T-C

111747139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760147-T-C

111747825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759424-T-C

http://identifiers.org/hco/3/GRCh38#111747837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45759412-C-A

111747933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759340-T-G

111747993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759270-G-C

111748226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759053-T-C

111748427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758747-A-G

111748774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758381-G-A

111748774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758381-G-T

111748946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758317-C-T

111749022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758243-T-C

111749066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758199-T-A

111749066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758199-T-C

111749405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757698-G-A

http://identifiers.org/hco/3/GRCh38#111749467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45757636-C-A

111749549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757554-T-C

111749763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757335-T-C

111749880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757219-A-T

111749881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757218-T-C

111750378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756730-T-C

111750418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756697-G-T

111750967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756125-T-A

111751158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755869-G-C

111751199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755835-G-A

111751446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755600-C-T

111751500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45755545-A-G

111752212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755143-G-A

http://identifiers.org/hco/3/GRCh38#111752218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45755137-A-C

111752246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755109-G-A

111752248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755107-C-G

111752250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755105-G-C

111752449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45754186-G-T

111758874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753823-G-T

http://identifiers.org/hco/3/GRCh38#111758916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45753774-C-A

111758947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753749-C-T

111758965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753731-A-G

111758974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753722-C-T

111759551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753068-C-T

111759568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753051-T-A

111759774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752871-C-T

111759775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752870-A-G

111759822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752823-C-G

111760072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751888-G-C

111760365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751618-G-C

111760365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751618-G-T

111760803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751229-G-A

111760844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751200-G-C

111761288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45751091-G-T

111761338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751039-G-T

111761394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750983-C-G

111761501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750879-A-G

111761638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750753-T-C

111761676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750715-C-T

111761796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750614-A-G

111761915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750493-A-G

111761984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750326-G-C

http://identifiers.org/hco/3/GRCh38#111761989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45750321-A-C

111761989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750321-A-G

http://identifiers.org/hco/3/GRCh38#111762049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45750285-C-A

111762049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750285-C-G

111762226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750106-A-G

111762417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749938-G-A

111762475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749880-C-T

111763306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749045-A-G

111763779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45748614-C-T

http://identifiers.org/hco/3/GRCh38#111764321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45748099-C-A

111764411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45748003-G-A

http://identifiers.org/hco/3/GRCh38#111764596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45747809-C-A

111764607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747798-C-T

111764714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747720-A-T

111764719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747716-A-G

http://identifiers.org/hco/3/GRCh38#111764832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45747635-C-A

111764931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747532-T-C

111764944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747519-T-A

111765168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45747315-C-T

111765614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746938-T-C

http://identifiers.org/hco/3/GRCh38#111765760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45746802-A-C

111765845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746713-T-G

111766084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746360-T-A

111767252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746194-G-T

111767609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745859-A-G

111767617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745846-A-G

111767678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745806-A-G

111767976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745551-G-A

111768171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745358-T-G

111768288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745248-A-G

http://identifiers.org/hco/3/GRCh38#111768322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45745214-A-C

111768798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744741-T-C

111768864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744676-T-C

111768867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744673-T-A

111769366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744167-A-G

111769379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744154-C-T

111769736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743819-C-G

111769828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743721-A-G

111769945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743334-A-G

111770439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742824-A-G

111770479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742787-G-A

111770941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742602-C-T

http://identifiers.org/hco/3/GRCh38#111770980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45742550-C-A

111771062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742487-T-C

111771086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742469-T-C

111771135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742421-A-T

111771151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742405-T-C

http://identifiers.org/hco/3/GRCh38#111771349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45742138-A-C

111771349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742138-A-T

111771715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45741718-G-A

111772087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740706-T-C

111772110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740684-T-C

111772156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740642-C-T

111772205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740592-T-C

111772493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740250-C-T

111772509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740234-C-T

111772673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740073-G-T

111772821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739970-G-C

111772873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739950-A-G

111772924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739902-C-T

111772977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739851-A-G

111772977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739851-A-T

http://identifiers.org/hco/3/GRCh38#111773047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45739792-A-C

111773117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739727-T-C

111773523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738752-C-T

http://identifiers.org/hco/3/GRCh38#111773617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45738657-C-A

111773817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738493-T-C

111773845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738454-C-G

111774131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738183-G-A

111774131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738183-G-T

111774535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737806-C-T

111774551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737790-G-C

111774794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737534-T-C

111774836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737492-G-A

111775264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737129-G-T

111775694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736370-A-G

111775800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736246-C-T

111775829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736217-T-C

http://identifiers.org/hco/3/GRCh38#111775841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45736205-A-C

111776293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735752-G-A

111776478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735668-C-T

111776643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735528-G-C

111776812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735362-T-A

111777443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734831-A-G

111777484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734788-A-G

111777484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734788-A-T

http://identifiers.org/hco/3/GRCh38#111779936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45732613-C-A

111779985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45732564-T-A

111779985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45732564-T-C

111779985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45732564-T-G

http://identifiers.org/hco/3/GRCh38#111780006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45732543-C-A

http://identifiers.org/hco/3/GRCh38#111781244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45731820-A-C

111781244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731820-A-G

111781344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731735-C-G

111781458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731631-A-G

111781683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731419-A-G

http://identifiers.org/hco/3/GRCh38#111781707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45731395-C-A

111781717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731385-C-T

111781798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45731302-G-T

111781933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45731164-G-A

111781966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45731142-A-G

http://identifiers.org/hco/3/GRCh38#111784047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45730090-C-A

111784248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45729887-T-G

111784450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45729674-T-C

111786850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725413-T-A

111786920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725343-G-A

111786930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725331-G-A

111786986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725275-A-G

111787318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45722075-C-T

111787595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721840-G-A

111787595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721840-G-T

111787722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721713-A-G

http://identifiers.org/hco/3/GRCh38#111788213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45721232-A-C

111788213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721232-A-G

http://identifiers.org/hco/3/GRCh38#111788292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45721154-C-A

111788293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721153-T-C

111788297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721149-T-C

111788447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720991-A-G

111788800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720723-G-T

111788890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 45720626-C-T

http://identifiers.org/hco/3/GRCh38#111789080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45720465-C-A

111789473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720064-A-T

111789506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720014-C-T

111789526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719999-A-G

111789526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719999-A-T

111789722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719835-T-G

111790133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719397-C-T

111790236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719295-A-G

111790281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719249-G-A

111790462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719059-C-G

111790486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719035-G-A

111790530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718991-C-G

111790530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718991-C-T

111791094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718215-A-G

111791094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718215-A-T

111791138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718163-G-A

http://identifiers.org/hco/3/GRCh38#111791280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45718069-C-A

111791324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718034-T-C

111791349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718009-T-A

http://identifiers.org/hco/3/GRCh38#111792248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45717808-C-A

111792372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717633-G-A

111792817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

111794592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45717432-T-C

111794771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717279-T-C

111795373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716776-C-T

111801682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45715148-C-T

111801862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714966-C-T

http://identifiers.org/hco/3/GRCh38#111801934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45714917-A-C

111801939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714912-T-G

111802205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714680-C-T

111802250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714635-C-T

111802294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714585-C-T

111802358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714541-C-G

http://identifiers.org/hco/3/GRCh38#111803036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45713825-A-C

111803241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45713655-A-G

http://identifiers.org/hco/3/GRCh38#111807154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45711875-A-C

111807866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45711581-G-C

111808486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710978-T-C

111808717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710904-C-G

111809144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45710436-T-G

111810439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708441-C-T

111810481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708371-G-T

111810530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708270-C-T

111810567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708195-T-C

111811235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707079-C-T

111811359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706954-G-A

111811402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706912-G-A

111811430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706884-G-T

111811640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706694-C-T

111811653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706681-C-T

http://identifiers.org/hco/3/GRCh38#111811665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45706669-C-A

111811665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706669-C-T

111811666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706668-G-A

111811702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706574-C-T

111811874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706425-T-A

111811939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706385-C-T

111812062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706285-G-C

111812075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706272-T-A

111812116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706221-G-C

111812116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706221-G-T

111812193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706125-T-C

111812317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706003-T-A

111812374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705950-C-T

111812570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704964-C-T

111812776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704762-A-G

111812817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704720-G-A

111812945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704594-C-G

111812945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704594-C-T

111813434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703493-T-C

http://identifiers.org/hco/3/GRCh38#111813664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45703277-A-C

http://identifiers.org/hco/3/GRCh38#111813779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45703176-C-A

111813779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703176-C-T

111819568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703019-T-C

111821191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701719-C-T

111821198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701712-C-T

111821204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701706-T-C

111821502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701355-G-A

111821567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701317-A-G

111821646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701241-A-G

http://identifiers.org/hco/3/GRCh38#111821801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45701105-C-A

111821801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701105-C-T

111822978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699078-G-C

111823410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698669-T-G

111823594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698490-A-G

111823883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698199-T-C

111823899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698180-G-T

111824731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696654-T-C

111824918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696515-T-C

111824973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696464-A-G

111825239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695898-A-T

111825255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695884-T-G

111825313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695834-G-C

111826774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693966-G-T

111826793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693947-A-T

111826857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693882-G-A

111827970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692054-G-A

111828063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691968-G-A

http://identifiers.org/hco/3/GRCh38#111828615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45691474-C-A

111828615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691474-C-G

111828934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691335-C-T

111829120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691154-C-T

111829121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691153-A-G

111829252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691036-G-A

111829993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690613-A-T

111830426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690204-T-C

111831249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689905-A-G

111831389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689761-A-T

111831390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689760-T-C

111831429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689721-A-G

http://identifiers.org/hco/3/GRCh38#111831539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45689603-A-C

111831539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689603-A-G

111831690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689453-C-T

111832174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688940-C-T

111832304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688851-T-C

111832318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688837-A-G

111832322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688833-C-T

111834633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687986-T-G

111834676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687943-G-C

111834731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687876-T-C

111834760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687850-A-G

111834761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687849-C-T

http://identifiers.org/hco/3/GRCh38#111834838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45687770-C-A

111834838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687770-C-T

111834997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687657-A-G

111835112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687479-C-T

111835214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687405-T-C

111835247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687372-G-A

111835364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687282-A-G

111835568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687107-C-G

111835734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686963-T-A

111835837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686891-G-A

111835837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686891-G-C

111835845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686883-G-C

111836045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686705-T-C

111837221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686550-G-A

http://identifiers.org/hco/3/GRCh38#111837241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45686534-A-C

111837252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686523-G-A

http://identifiers.org/hco/3/GRCh38#111837293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45686479-A-C

111837293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686479-A-T

111837360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686418-A-G

111837431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686350-T-A

111838692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685952-T-G

111838891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685816-C-T

111839207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685509-A-T

http://identifiers.org/hco/3/GRCh38#111839303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45685442-A-C

111839421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685343-T-A

http://identifiers.org/hco/3/GRCh38#111844450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45683137-A-C

111844450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45683137-A-T

111844542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682856-C-T

111844590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682775-C-T

111844641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682739-C-T

111844750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682629-T-C

111845479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682259-T-A

111845479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682259-T-G

111845664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45680975-G-A

111845718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45680911-G-A

111845836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45680782-A-G

111845885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45680733-C-T

http://identifiers.org/hco/3/GRCh38#111845985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45680640-C-A

111845985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45680640-C-T

111845993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45680628-T-C

111846262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679941-G-A

111846262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679941-G-T

http://identifiers.org/hco/3/GRCh38#111846287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679916-C-A

http://identifiers.org/hco/3/GRCh38#111846288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679915-A-C

111846412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679792-T-C

http://identifiers.org/hco/3/GRCh38#111846567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679665-C-A

111846567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45679665-C-T

111846691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45679541-G-A

http://identifiers.org/hco/3/GRCh38#111846788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679438-C-A

111846975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45679253-T-C

111847045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45679198-A-G

111847246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678996-A-G

111847386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678865-G-A

111847454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678801-G-C

111847461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678794-T-C

111847523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678732-G-T

111847958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45678157-T-A

111847992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45678124-G-A

111848033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45678091-G-A

111848097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45678027-C-T

111848106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45678018-A-G

111848140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45677986-T-C

http://identifiers.org/hco/3/GRCh38#111848160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45677967-A-C

111848187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45677941-T-C

111848308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677812-C-T

111848309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677811-G-A

111848309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677811-G-C

111848363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677766-G-A

111848549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677574-A-G

111848549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677574-A-T

111848559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677564-G-C

http://identifiers.org/hco/3/GRCh38#111848596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45677530-A-C

111848625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677506-A-G

111848641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45677490-T-C

111849428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45677234-C-T

111849520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45677142-G-A

111851413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45676258-G-A

111851630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45676060-T-A

111851651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45676039-T-C

http://identifiers.org/hco/3/GRCh38#111851976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45675723-A-C

111851976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45675723-A-T

111852064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675641-A-G

111852087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675617-T-C

111852094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675610-G-A

http://identifiers.org/hco/3/GRCh38#111852189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45675458-C-A

111852189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675458-C-T

111852781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675134-C-T

111852783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675132-T-C

111852785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45675130-C-T

http://identifiers.org/hco/3/GRCh38#111853092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45674619-C-A

111853511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45674186-G-T

111853512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45674185-C-T

111855286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45670331-C-G

111855288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45670329-C-G

111855304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45670309-A-G

111855319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45670291-G-A

111855330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45670280-T-C

111856108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45669696-A-G

111856164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45669638-T-C

111856269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45669565-T-C

111856279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45669555-A-G

111856822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45669049-T-C

111858612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665850-G-T

111858859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665613-G-A

111859065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665438-G-A

111859065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665438-G-C

111859065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665438-G-T

111859099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665403-G-A

111859099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665403-G-C

111859100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665402-A-G

111859127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665375-G-A

111859164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665342-C-T

111859175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665329-T-A

111859175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45665329-T-C

111859207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665300-A-G

111859207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665300-A-T

111859275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665188-T-C

http://identifiers.org/hco/3/GRCh38#111859305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45665158-A-C

111859334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665129-A-G

111859361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665101-C-T

111859416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665049-G-A

111859416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665049-G-T

111859426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665039-T-C

111859454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45665012-C-T

http://identifiers.org/hco/3/GRCh38#111859557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45664920-C-A

111859592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664884-T-G

111859593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664883-G-T

111859617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664858-G-A

111859683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664792-C-T

111859721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664755-A-G

111859721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664755-A-T

111859750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664727-C-T

111859781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664696-G-A

111859781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664696-G-T

111859783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664694-G-T

http://identifiers.org/hco/3/GRCh38#111859800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45664649-C-A

111859807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664642-G-A

111859807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664642-G-T

111859836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664613-G-A

111859836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45664613-G-T

http://identifiers.org/hco/3/GRCh38#111859960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45664486-C-A

111859960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664486-C-T

http://identifiers.org/hco/3/GRCh38#111860006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45664445-C-A

111860006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664445-C-T

111860007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664444-A-G

111860007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664444-A-T

111860204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664279-G-T

111860223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664260-T-C

111860272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664227-C-T

http://identifiers.org/hco/3/GRCh38#111860506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45663985-C-A

111860506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45663985-C-T

111860838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45663669-G-C

111860912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45663598-T-C

111861890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662681-G-A

111861914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662655-T-C

111862253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662528-G-T

http://identifiers.org/hco/3/GRCh38#111862439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45662366-C-A

111862474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662332-A-G

111862475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662331-A-T

111862666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45662130-G-A

111862822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661983-G-A

111862909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661909-C-T

111863001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661821-G-C

111863202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661626-C-T

111863305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661525-T-A

111863448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661411-G-T

111863534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45661332-C-G

111863886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45659868-C-G

111863905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45659849-A-G

111864155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45659619-G-A

111864543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45659234-A-G

111864603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45659171-G-A

111864920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45658854-A-G

111864922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45658852-A-G

111864947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45658829-A-G

111865037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45658738-A-G

111865106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45658671-G-C

111865189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45658598-G-A

111865244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45658543-G-A

111865254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45658533-C-T

http://identifiers.org/hco/3/GRCh38#111865589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45658196-A-C

111865654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45658125-G-A

http://identifiers.org/hco/3/GRCh38#111865984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45657370-C-A

111866463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656777-A-G

111866475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656765-G-A

111866475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656765-G-T

111866696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656549-T-A

111866778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656451-C-G

111866778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656451-C-T

111866838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656377-G-A

111866838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45656377-G-T

111867347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45655092-A-G

111867376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45655062-T-C

111867385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45655053-T-C

111868670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45653128-T-C

111868897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652917-G-A

111868947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652865-A-G

111869075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652738-G-A

111869152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652665-G-C

111869179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652653-A-G

111869319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652517-T-A

111869376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652473-T-A

111869443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652412-A-T

111869556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45652312-C-T

111870112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651769-A-T

111870184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651705-G-C

111870256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651645-G-A

111870256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651645-G-C

111870258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651643-T-C

111870730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651165-G-A

111870807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45651093-A-G

111871020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650870-G-T

111871132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650782-G-A

111871719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650560-C-G

111871829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650451-T-G

111871975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650305-A-T

111872046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650229-G-A

111872046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650229-G-C

111872279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45650006-A-G

111872327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649958-A-G

111872423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649881-C-G

http://identifiers.org/hco/3/GRCh38#111872530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45649767-A-C

111872534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649763-A-T

111872620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649686-C-G

111872819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649494-G-A

111872850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45649462-T-C

111882077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648229-T-C

111882097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648210-A-G

111882119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648188-T-C

111882165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648148-T-C

111882175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648138-A-G

111882186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45648126-C-G

111882580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45647747-A-G

111882846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45647466-C-G

111883252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45647136-A-G

111883509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45646852-T-C

111884074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 45646446-G-A

111884157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45646363-T-C

111884195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45646325-C-G

111884341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: synonymous variant
orthologous variants: 45646179-C-T

111884504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45646019-T-C

111884634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45645889-G-A

111884661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45645862-G-C

111884761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: synonymous variant
orthologous variants: 45645762-G-A

111884840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45645683-T-C

111885083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: stop gained
orthologous variants: 45645440-C-T

111885309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45645223-A-G

111885309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45645223-A-T

111885527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45645010-G-A

111885527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45645010-G-T

111885782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45644649-C-G

111885836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45644609-G-A

111885876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45644569-G-A

111886031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45644405-A-G

111886311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45644100-A-G

111886818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45643849-T-A

111886832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45643833-T-C

111887325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45643356-C-T

111890404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45641393-T-G

111890415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45641382-T-C

111890517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45641324-C-G

http://identifiers.org/hco/3/GRCh38#111890612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45641230-A-C

111890778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45641089-T-C

http://identifiers.org/hco/3/GRCh38#111890801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45641069-C-A

http://identifiers.org/hco/3/GRCh38#111890882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45641004-C-A

111891146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45640759-A-G

111892211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45640280-T-C

111892324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45640160-C-T

111892373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45640111-A-G

111892410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45640080-T-C

111892854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638908-G-A

111892882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638880-A-G

111892882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638880-A-T

111892989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638784-G-A

111893089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638671-T-C

111893100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638657-C-G

111893557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638208-C-G

111893600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638170-G-A

111893600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638170-G-T

http://identifiers.org/hco/3/GRCh38#111893631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45638142-A-C

111893631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638142-A-T

111893646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638129-T-A

111893699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45638072-G-T

111894824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45637679-C-G

111894840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45637663-G-C

111894861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45637645-T-G

111894972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45637567-A-G

http://identifiers.org/hco/3/GRCh38#111895045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45637494-A-C

111895045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45637494-A-G

111895215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45637303-G-A

111895320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45637182-T-C

111895328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45637175-G-A

111895545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45636967-C-T

111895575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45636938-T-C

111896687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45636767-C-T

111896753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45636701-T-A

111901614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45636143-T-A

111901789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45635981-G-T

111901883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45635900-A-G

111901949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45635841-T-C

111902031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45635737-C-T

111902070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45635701-C-T

111903387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634971-C-T

111906404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634847-G-A

111906426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634824-C-G

111906582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634687-T-C

111906632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634644-G-A

111906634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634642-T-C

111906702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634576-T-C

111906871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634384-C-T

111906874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45634366-A-G

111907239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633958-A-G

111907301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633898-G-T

http://identifiers.org/hco/3/GRCh38#111907394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45633817-A-C

111907446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633765-G-A

111907489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633731-T-C

111907499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633712-T-G

111907509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633702-T-C

111907566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633651-G-T

111907821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633458-G-C

http://identifiers.org/hco/3/GRCh38#111907914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45633376-A-C

111908456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633132-A-G

111908543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45633038-T-A

111908748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632844-T-C

111908748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632844-T-G

111908752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632840-A-G

111908768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632823-A-G

111908894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632683-T-C

111909648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632515-T-A

111909895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632297-T-C

111910036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632174-C-T

111910056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45632144-A-G

http://identifiers.org/hco/3/GRCh38#111910212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45631951-C-A

111910225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631938-C-T

111910461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631768-C-T

111910496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631741-G-A

111910612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631714-G-A

111910773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631565-C-T

111911055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45631284-C-T

111911248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631087-T-A

111911298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631048-G-C

111911339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45631004-G-A

111911507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45630841-A-T

http://identifiers.org/hco/3/GRCh38#111911564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45630786-C-A

111911790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45630582-G-T

111911819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45630554-A-G

111912190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45630214-T-C

111912574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45629601-A-G

111912711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45629473-G-T

111912918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45629276-G-A

111913080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45629066-A-G

http://identifiers.org/hco/3/GRCh38#111913290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45628897-C-A

111913364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45628825-A-G

111913364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45628825-A-T

http://identifiers.org/hco/3/GRCh38#111913386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45628800-C-A

111913397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45628789-A-G

111913538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45628648-T-G

111913717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45628476-G-A

111913717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45628476-G-T

111913736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45628457-A-G

111913762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45628431-G-A

http://identifiers.org/hco/3/GRCh38#111913798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45628406-A-C

111913798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45628406-A-T

111915760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45627476-T-G

111915783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45627451-G-T

111915798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45627436-G-T

111915801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45627433-C-T

111915895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626985-A-G

http://identifiers.org/hco/3/GRCh38#111915905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45626975-C-A

111915921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626961-T-C

111915937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626945-G-T

111915947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626940-T-C

111915955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626932-A-G

http://identifiers.org/hco/3/GRCh38#111915968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45626919-C-A

111916011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626879-T-C

111916042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626845-G-A

111916042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626845-G-T

111916211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626700-T-A

111916211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626700-T-C

111916275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626648-A-G

111916293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626634-A-G

111916301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45626626-T-C

111916663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626291-G-A

http://identifiers.org/hco/3/GRCh38#111916673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45626273-A-C

111916700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626246-G-A

111916740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626184-C-T

111916741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626183-T-C

111916773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626164-A-G

111916800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626130-A-G

111916928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45626004-T-C

111916996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45625905-T-C

http://identifiers.org/hco/3/GRCh38#111917038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45625859-C-A

111917080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45625817-G-T

http://identifiers.org/hco/3/GRCh38#111917100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45625794-C-A

111917195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45625523-G-A

111917195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45625523-G-T

111917292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45625424-A-G

http://identifiers.org/hco/3/GRCh38#111917313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45625404-C-A

111917313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45625404-C-T

http://identifiers.org/hco/3/GRCh38#111917477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45625253-C-A

111917479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45625251-G-T

111917517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45625213-C-G

111917947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45624464-G-A

111917994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45624418-G-A

111918202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45624216-G-A

111918208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45624210-C-T

http://identifiers.org/hco/3/GRCh38#111918253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45624171-A-C

111918353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45624069-C-T

111918456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623964-C-G

111918636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623769-A-G

111918733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623620-A-T

111918932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623428-G-A

111918932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623428-G-C

111918932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623428-G-T

http://identifiers.org/hco/3/GRCh38#111918962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45623309-C-A

111918962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623309-C-T

http://identifiers.org/hco/3/GRCh38#111918963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45623308-A-C

111918963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623308-A-G

111918963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623308-A-T

111918967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623304-G-A

111918967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623304-G-C

111918967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623304-G-T

http://identifiers.org/hco/3/GRCh38#111918969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45623302-A-C

111918969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623302-A-G

111918969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623302-A-T

http://identifiers.org/hco/3/GRCh38#111918986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45623288-C-A

111919015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623257-T-G

111919023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623249-T-C

111919043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45623229-T-A

111919150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense variant
orthologous variants: 45623122-A-T

111919222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45623030-T-C

111919297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622901-A-G

111919297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622901-A-T

http://identifiers.org/hco/3/GRCh38#111919300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45622899-C-A

111919318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622881-A-G

111919318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622881-A-T

111919344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622855-T-C

111919354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622845-A-G

111919354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622845-A-T

111919356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622843-A-G

111919356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622843-A-T

111919738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45622487-G-C

111920198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622065-G-A

http://identifiers.org/hco/3/GRCh38#111920199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45622064-C-A

111920199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622064-C-T

http://identifiers.org/hco/3/GRCh38#111920214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45622049-C-A

111920254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45622018-A-T

111920444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621830-C-G

111920505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621764-G-A

111920505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621764-G-T

111920573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621692-T-G

111920784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621481-G-A

111921160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621159-G-A

111921218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45621101-C-T

111921554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45620772-T-A

111921586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45620740-G-A

111921586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45620740-G-T

111922110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45620086-T-C

111922294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45619942-C-T

111923281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45619074-G-A

http://identifiers.org/hco/3/GRCh38#111923491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45618408-A-C

111923491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45618408-A-G

111923491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45618408-A-T

111923638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45618274-C-T

111923700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45618209-T-C

111923824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45618110-T-A

111923925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45617981-A-G

111924043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617855-T-C

111924204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617702-C-G

111924204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617702-C-T

111924210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617696-G-T

111924351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617562-T-C

111924351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617562-T-G

111924417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617499-T-G

111924421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45617495-T-C

111924605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45617305-T-C

111924605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45617305-T-G

111924732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45617178-T-C

111924733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45617177-A-G

111925247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45616570-A-G

111925247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45616570-A-T

111925668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45615972-A-G

111926082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45615538-T-A

111926082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45615538-T-C

111926108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45615526-A-G

111926468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45615163-T-C

111926564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45615062-A-G

111927558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45614816-T-C

111927630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45614741-G-A

111927933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613879-T-C

111928110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613698-A-G

111928449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613113-T-C

111928449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613113-T-G

111928473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613089-A-G

111928507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613057-T-C

111928545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45613001-A-G

http://identifiers.org/hco/3/GRCh38#111928752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45612487-A-C

111928752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45612487-A-G

111928779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45612460-G-T

111928798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45612441-C-T

111929283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45612248-A-G

111929615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611947-G-C

111930202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611652-T-C

111930217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611637-T-G

http://identifiers.org/hco/3/GRCh38#111930293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45611560-C-A

111930688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611195-G-A

111930688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611195-G-T

111930855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45611056-G-T

111931075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610821-A-G

111931077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610819-G-A

111931093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610809-A-G

111931211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610732-T-C

111931300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610657-A-G

111931519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610265-C-T

111931523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610261-C-T

111931681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45610068-C-T

111931753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609979-G-A

111931810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609928-C-T

111931937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609798-C-T

111932196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609553-A-G

111932236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609514-T-C

http://identifiers.org/hco/3/GRCh38#111932541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45609212-C-A

111932541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609212-C-T

111932559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45609193-T-C

111932871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45608946-T-G

111933594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607947-T-A

111933858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607687-C-T

http://identifiers.org/hco/3/GRCh38#111933865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45607680-C-A

111934124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607442-C-T

http://identifiers.org/hco/3/GRCh38#111934379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45607236-A-C

111934506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607140-A-G

111934506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607140-A-T

111934507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45607139-A-G

111936513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45605174-A-G

111936542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45605153-T-C

111936698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45605011-C-T

111936836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45604886-A-G

111936890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45604823-G-C

111936980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45604744-T-C

111936986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45604738-G-A

111937180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45604347-C-T

111937240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, undefined
orthologous variants: 45604290-A-G

111938051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45603861-G-T

111938466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602802-C-T

111938563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602717-A-T

111938605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602490-A-G

111938617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602471-G-T

111938638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602449-T-C

111938887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602267-C-T

http://identifiers.org/hco/3/GRCh38#111939093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45602140-C-A

111939131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602098-C-T

111939161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45602077-T-C

http://identifiers.org/hco/3/GRCh38#111939251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45602001-C-A

111939264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45601988-A-G

111939350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45601939-T-G

111939395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45601897-G-A

111939395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45601897-G-T

http://identifiers.org/hco/3/GRCh38#111939460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45601833-C-A

http://identifiers.org/hco/3/GRCh38#111939550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45601743-C-A

111939550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45601743-C-G

111939749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601506-T-A

111939756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601499-T-A

111939761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601494-T-C

111939779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601476-G-T

111939915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45601337-T-C

111940304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600949-A-G

111940338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600914-C-T

http://identifiers.org/hco/3/GRCh38#111940386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45600866-C-A

111940386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600866-C-T

111940450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600803-A-G

111940450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600803-A-T

111940714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600564-T-C

111940758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600498-G-C

111940760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600496-A-G

111940760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600496-A-T

111940783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600472-T-A

111940803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600452-C-G

111940811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600444-C-T

111940865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600398-T-C

111940865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600398-T-G

111940899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45600366-T-C

111943883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45599315-T-A

111943883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45599315-T-G

111944231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598999-A-G

111944510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598760-T-C

111944511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598759-A-G

http://identifiers.org/hco/3/GRCh38#111944512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45598758-A-C

111944628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598655-G-A

111944733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598539-T-C

111944733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598539-T-G

111944812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598476-A-G

111945120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598305-T-G

111945251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598180-G-A

111945251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45598180-G-T

111945319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45598112-G-A

111945319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45598112-G-C

111945399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45598030-A-G

111945399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45598030-A-T

111945506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45597932-A-G

111946477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45597723-A-G

111946708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45597500-A-G

111946842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45597367-T-C

111947318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45596908-G-A

http://identifiers.org/hco/3/GRCh38#111947454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45596812-C-A

111947623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45596641-A-G

111948197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45596043-G-T

111948231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45596006-T-C

http://identifiers.org/hco/3/GRCh38#111948442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45595865-A-C

111948484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45595822-G-A

111948484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45595822-G-T

http://identifiers.org/hco/3/GRCh38#111948858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45595522-C-A

111948858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45595522-C-T

111949010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45595370-G-A

111949269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45595128-A-T

111949599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594815-T-C

111949727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45594681-T-C

111949727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45594681-T-G

111949741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45594667-G-A

111949741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45594667-G-T

111949807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45594604-G-A

111949903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594513-T-C

http://identifiers.org/hco/3/GRCh38#111950035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45594391-C-A

111950171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594294-A-G

111950181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594284-G-A

111950197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594268-C-T

111950262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45594209-C-T

111951429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45593445-T-C

111952079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45593118-G-A

111952079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45593118-G-T

111952256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592935-T-G

http://identifiers.org/hco/3/GRCh38#111952333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45592861-C-A

111952461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592750-A-G

111952491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592713-A-G

111952491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592713-A-T

http://identifiers.org/hco/3/GRCh38#111952496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45592708-C-A

111952660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, missense_variant
orthologous variants: 45592548-C-T

111952746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592463-C-T

http://identifiers.org/hco/3/GRCh38#111952813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45592397-A-C

111952813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592397-A-G

111952820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592390-A-G

http://identifiers.org/hco/3/GRCh38#111952840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45592370-C-A

111952898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592315-G-A

111952980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592242-G-A

111952994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45592229-C-T

111953256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591974-C-T

111953543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591537-T-G

111953622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591456-C-T

111953626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591452-T-C

111953659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591420-C-T

111953749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron variant
orthologous variants: 45591328-G-T

111953858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45591210-G-C

111953858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45591210-G-T

111953880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45591189-G-A

111953880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45591189-G-T

111953978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45591084-C-T

111954052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45591016-G-A

111954060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45591008-C-T

111954163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590913-T-A

111954229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590827-C-T

111954361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590710-A-G

111955053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590043-C-G

111955053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590043-C-T

http://identifiers.org/hco/3/GRCh38#111955082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45590020-C-A

http://identifiers.org/hco/3/GRCh38#111955165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45589950-C-A

111956285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589167-C-T

http://identifiers.org/hco/3/GRCh38#111956651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45588856-A-C

111956783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588738-G-C

111956943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588583-T-G

http://identifiers.org/hco/3/GRCh38#111957039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45588482-C-A

111957129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588387-C-T

111957130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45588386-T-C

111957130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45588386-T-G

111957460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588047-G-A

http://identifiers.org/hco/3/GRCh38#111957506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45588002-C-A

111957506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588002-C-T

111957550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587959-G-T

111957578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587931-G-T

111957837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587689-C-T

111957972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587333-G-A

111957972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587333-G-T

111958039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587252-T-G

111958117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587176-A-G

111958136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587158-T-G

111958144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587150-G-A

http://identifiers.org/hco/3/GRCh38#111958164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45587136-C-A

111958164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587136-C-T

http://identifiers.org/hco/3/GRCh38#111958217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45587088-C-A

111958217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45587088-C-T

111958305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587008-G-A

111958305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45587008-G-T

http://identifiers.org/hco/3/GRCh38#111958311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45587003-C-A

111958323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586991-A-G

http://identifiers.org/hco/3/GRCh38#111958350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45586968-C-A

111958426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586892-T-C

111958427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586891-G-A

111958455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586863-T-C

111958491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586830-C-T

111958547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586774-T-C

111958578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586744-G-A

111958796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586552-A-G

111958805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586545-G-T

111958866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586484-G-A

http://identifiers.org/hco/3/GRCh38#111959037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45586325-C-A

111959072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586285-C-T

111959122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586246-C-G

111959220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45586157-T-C

111959368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585865-G-A

111959506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585744-C-T

111960193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585053-G-A

111960246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585001-T-A

111960246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45585001-T-C

111960310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584937-T-C

111960312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584935-T-C

111960356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584891-A-G

111960392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584859-A-G

111960556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584705-A-G

111960598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584665-A-T

111960694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584558-G-T

111960740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584515-T-G

111960762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584493-A-G

http://identifiers.org/hco/3/GRCh38#111960768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45584487-C-A

111961392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45584208-A-G

111961620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583962-T-C

111961702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583889-T-A

111961702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583889-T-C

111961767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583829-G-C

111961800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583800-T-C

111961863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583705-A-G

111961863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583705-A-T

http://identifiers.org/hco/3/GRCh38#111961888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45583679-C-A

111961912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583655-C-T

http://identifiers.org/hco/3/GRCh38#111961947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45583619-C-A

111961947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45583619-C-T

111962028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45583555-G-A

111962028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45583555-G-T

http://identifiers.org/hco/3/GRCh38#111962040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45583543-C-A

111962040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45583543-C-G

111962242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45583341-A-G

111962242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45583341-A-T

111962245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45583338-C-G

http://identifiers.org/hco/3/GRCh38#111962296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45583287-C-A

111962319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45583264-T-A

111962319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45583264-T-C

111962329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583254-G-T

http://identifiers.org/hco/3/GRCh38#111962413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45583192-A-C

111962413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583192-A-G

111962450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583162-G-T

111962457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583155-T-C

111962463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583149-T-C

111962647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45583021-G-A

111962700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582973-T-C

http://identifiers.org/hco/3/GRCh38#111963084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45582656-C-A

111963084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582656-C-T

111963189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582514-G-C

111963208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582497-C-G

111963227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45582480-C-T

111963902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45581392-T-A

111964217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580858-T-G

111964330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580747-A-G

111965319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45580567-C-T

111966250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579092-T-G

111966475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578869-T-A

111966475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578869-T-C

111966475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578869-T-G

111966483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578861-T-A

111966483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578861-T-C

111966483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578861-T-G

http://identifiers.org/hco/3/GRCh38#111966488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45578856-C-A

111966488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578856-C-T

111966502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578839-T-A

111966502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578839-T-C

111966502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578839-T-G

111966531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578776-T-A

111966531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578776-T-C

111966531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578776-T-G

111966544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578763-G-A

111966544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578763-G-C

111966544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578763-G-T

http://identifiers.org/hco/3/GRCh38#111966573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45578607-C-A

111966573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578607-C-G

111966709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578472-C-T

111966737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578445-A-G

http://identifiers.org/hco/3/GRCh38#111966767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45578411-A-C

111966767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578411-A-G

111966770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578408-A-G

111966785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578400-T-C

111966786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578399-T-A

111966795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578390-G-A

111966795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578390-G-C

111966795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578390-G-T

111967138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578079-A-G

111967345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577867-T-G

111967422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577827-T-C

111967640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577647-T-A

111967681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45577603-C-G

111967681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45577603-C-T

111967748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45577536-G-A

http://identifiers.org/hco/3/GRCh38#111967835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45577449-C-A

111967835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577449-C-T

111967881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577402-G-A

111967881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577402-G-T

111967898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577385-G-A

111967898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577385-G-T

http://identifiers.org/hco/3/GRCh38#111967939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45577364-C-A

111967939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577364-C-T

111967973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577332-T-A

111967973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45577332-T-G

111968020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577307-C-G

111968238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573321-C-T

111968377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573191-C-G

111968460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573111-T-A

111968481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573090-T-C

111968481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573090-T-G

111968497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573074-A-G

111968519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573057-A-G

111968681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572901-G-A

111968928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572669-C-T

111968992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572570-T-A

111968992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572570-T-C

111969076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572488-T-A

111969077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572487-C-T

111969495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572136-A-G

http://identifiers.org/hco/3/GRCh38#111969542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45572093-C-A

111969578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572065-T-C

111969932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571650-G-A

111970348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571227-T-C

111973595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569308-T-C

111973755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45569150-G-A

111973794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45569111-G-C

111973794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45569111-G-T

111973806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45569099-A-T

111973904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568811-G-T

111973937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568778-A-T

111973949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568761-A-G

111974382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568332-A-G

111974604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45568111-A-G

111974656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45568059-A-T

http://identifiers.org/hco/3/GRCh38#111974931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45567809-C-A

111974931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45567809-C-T

111975181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45567611-T-C

111975230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45567580-G-A

111975288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45567512-G-A

111975351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45567452-G-T

http://identifiers.org/hco/3/GRCh38#111975401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45567402-A-C

111976283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566523-G-T

111976293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566513-A-T

111976350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29573
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566455-A-G