6909331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 36739858-A-G

6909381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5 prime UTR variant
orthologous variants: 36739820-G-C

6909381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5 prime UTR variant
orthologous variants: 36739820-G-T

http://identifiers.org/hco/4/GRCh38#6909453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36739749-C-A

http://identifiers.org/hco/4/GRCh38#6909514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36739688-C-A

6909514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739688-C-T

http://identifiers.org/hco/4/GRCh38#6909517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36739685-C-A

6909517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739685-C-T

6909524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739679-G-A

6909572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739632-C-T

6909577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739627-C-G

6909577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739627-C-T

6909583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739621-G-A

6909583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739621-G-T

6909590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739614-T-C

6909634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739572-G-A

6909634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739572-G-T

6909687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739504-G-C

6909762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36739293-G-T

http://identifiers.org/hco/4/GRCh38#6909785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36739199-C-A

6909785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739199-C-G

6909785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739199-C-T

6909789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739195-G-A

6909789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36739195-G-T

6909816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36739158-G-A

6909816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36739158-G-T

6909822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36739152-G-A

6909844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36739133-C-G

6909844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36739133-C-T

6909865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36739114-T-A

6909891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36739088-G-A

6909989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738991-G-A

6909989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738991-G-T

6910045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738946-G-T

6910055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738938-G-A

6910055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738938-G-T

6910219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36738625-C-G

6910219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36738625-C-T

6910228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36738595-G-A

6910228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36738595-G-T

6910269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738550-G-A

6910290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738517-G-A

http://identifiers.org/hco/4/GRCh38#6910296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738511-C-A

http://identifiers.org/hco/4/GRCh38#6910299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738508-C-A

6910345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738450-T-C

http://identifiers.org/hco/4/GRCh38#6910379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738392-C-A

6910379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36738392-C-T

http://identifiers.org/hco/4/GRCh38#6910409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738364-C-A

http://identifiers.org/hco/4/GRCh38#6910441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738331-C-A

6910441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738331-C-G

6910442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738330-T-C

http://identifiers.org/hco/4/GRCh38#6910464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738272-C-A

http://identifiers.org/hco/4/GRCh38#6910472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738264-C-A

6910472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738264-C-G

6910472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738264-C-T

6910473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36738263-T-A

6910473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36738263-T-C

6910478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36738258-C-T

http://identifiers.org/hco/4/GRCh38#6910525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738226-C-A

6910525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738226-C-G

6910525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36738226-C-T

http://identifiers.org/hco/4/GRCh38#6910736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738026-C-A

6910736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738026-C-G

6910736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36738026-C-T

http://identifiers.org/hco/4/GRCh38#6910747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36738009-C-A

6910747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36738009-C-T

6910829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737918-G-C

6910857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737890-C-T

6911112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737656-G-A

6911112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737656-G-C

6911461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737268-C-T

6911698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737094-T-C

6911698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737094-T-G

6911777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36737022-C-T

6912457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736814-T-C

6912457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736814-T-G

6912708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736593-C-T

6912709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736592-A-G

6912710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736591-C-T

6912762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736540-T-C

6912813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36736489-T-A

6914343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36735012-C-T

6914374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36734983-A-G

6914519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36734869-G-A

6916278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36734103-T-G

6916370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36734007-A-G

6916382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36733995-C-T

6916398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36733979-C-T

6916403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36733974-T-G

6916826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36733554-G-T

6917123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36733304-C-G

6917148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36733280-T-G

6917239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36733197-A-G

6917255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36733181-T-A

6917759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36732775-G-A

6917759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36732775-G-C

6917812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36732726-A-G

6917842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36732696-T-C

6917854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36732684-A-G

6917899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36732629-C-T

6918400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731814-G-T

6918409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731805-T-G

6918521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731723-T-G

6919055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731250-G-A

6919267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731234-T-C

6919531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36731096-T-C

6920773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36730582-C-T

6922280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36730449-T-A

6922355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36730384-C-T

6922730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729942-C-T

6922820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729763-G-A

6923280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729486-T-C

6923280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729486-T-G

http://identifiers.org/hco/4/GRCh38#6923288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36729478-A-C

6923288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729478-A-G

http://identifiers.org/hco/4/GRCh38#6923290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36729476-C-A

6923290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729476-C-G

6923290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729476-C-T

6923315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729447-G-A

6923315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36729447-G-T

6923498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36729254-G-A

6923522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36729227-G-C

6923705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36729044-G-A

6923705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36729044-G-C

http://identifiers.org/hco/4/GRCh38#6923741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36729008-A-C

6923741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36729008-A-G

6923774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36728975-A-G

6923774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36728975-A-T

http://identifiers.org/hco/4/GRCh38#6923783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36728966-A-C

6923783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36728966-A-G

6924040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36728709-G-A

6924040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36728709-G-C

6924041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36728708-G-T

6924148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728601-T-C

6924169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728581-T-A

http://identifiers.org/hco/4/GRCh38#6924174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36728572-C-A

6924174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728572-C-T

6924220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728529-G-A

6924220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728529-G-C

6924220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728529-G-T

http://identifiers.org/hco/4/GRCh38#6924224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36728525-C-A

6924224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728525-C-T

6924290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728459-G-A

6924427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728304-C-G

6924612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728137-G-A

6924656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728093-A-G

6924671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36728079-C-T

6924782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727955-A-G

6924834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727905-T-C

6925405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727672-C-T

6925408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727669-C-T

6925556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727532-A-G

6925743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727375-C-T

6925854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727268-C-G

6925854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727268-C-T

6926060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727063-C-T

6926094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36727028-G-A

6926129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36726998-T-C

6926137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36726991-G-A

http://identifiers.org/hco/4/GRCh38#6926245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36726881-A-C

6927320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725998-A-G

6927660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725697-G-C

6927742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725629-G-A

6927742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725629-G-T

6927919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725439-G-A

6927919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725439-G-T

6927922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725436-C-T

6928295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725247-G-C

6928388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36725153-A-G

6928834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723744-G-C

6928977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723611-A-T

6929083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723502-G-C

6929083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723502-G-T

6929114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723474-G-A

6929324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36723268-G-A

6936481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36722648-C-T

6936501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36722627-T-C

http://identifiers.org/hco/4/GRCh38#6936659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36722480-C-A

6936863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36722315-A-T

6937480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721515-G-A

6937487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721504-A-G

6937590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721400-T-C

6937963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721103-G-C

6938027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721039-C-G

6938027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36721039-C-T

6938166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36720914-A-G

6938680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36720388-G-A

6939054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36720053-C-G

6939054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36720053-C-T

6939214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36719900-C-T

6939255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36719854-G-A

6939259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36719850-C-T

6939579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36719547-A-G

6940164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36719076-C-T

6940373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36718861-C-T

6944354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36718116-A-G

http://identifiers.org/hco/4/GRCh38#6944399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36718093-C-A

6944399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36718093-C-T

6944658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36717821-T-C

6944944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36717430-G-A

6944950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36717424-T-G

http://identifiers.org/hco/4/GRCh38#6945182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36717224-C-A

6946256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36716385-G-A

6946757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36716220-T-A

6947680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36715665-T-A

6947962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36715437-G-A

6948562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36714839-C-T

6948607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36714789-G-A

6948607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36714789-G-T

http://identifiers.org/hco/4/GRCh38#6948727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36714610-A-C

6948727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36714610-A-G

6948727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36714610-A-T

http://identifiers.org/hco/4/GRCh38#6952771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36711760-C-A

6952805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36711726-T-C

6952928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36711598-A-G

6953949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36710900-C-T

6954081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36710751-T-C

6954156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36710680-T-A

6954210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36710636-G-A

6954210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36710636-G-C

6954210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36710636-G-T

6954406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36710453-C-T

http://identifiers.org/hco/4/GRCh38#6954436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36710418-C-A

6954436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36710418-C-T

6954446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36710408-T-G

6955766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36709755-T-C

6955904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36709653-C-G

6955904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36709653-C-T

6957215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707964-A-G

6957289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707906-A-T

6957439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707763-T-G

6957618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707592-A-G

6957662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707548-T-A

6958081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707483-A-G

6958093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707471-C-G

6958223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707358-C-T

6958234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36707347-A-G

6959444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706979-C-T

6959480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706943-G-A

6959480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706943-G-C

http://identifiers.org/hco/4/GRCh38#6959671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36706788-A-C

6959671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706788-A-G

6959705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706744-T-C

http://identifiers.org/hco/4/GRCh38#6959794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36706660-A-C

6960005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36706054-A-G

http://identifiers.org/hco/4/GRCh38#6960640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36705764-A-C

6960859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36705558-C-T

6960910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36705495-G-A

6961010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36705406-G-A

6961067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36705355-T-G

6961277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36705110-T-G

6961854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704518-G-A

6961953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704433-G-A

6961956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704429-C-T

6962139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704334-G-A

6962139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704334-G-C

6962369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704176-G-T

6962413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36704144-G-T

6962976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36702689-T-A

6963047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36702635-T-A

6963098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36702589-C-T

6964192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36702010-C-T

6964298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701938-T-C

6964315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701922-C-T

6964325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701917-G-T

6964336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701906-C-T

6964432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701813-C-G

6964446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701799-G-A

http://identifiers.org/hco/4/GRCh38#6964572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36701689-A-C

6966276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36701293-T-C

6967470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700499-A-G

6967485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700484-A-G

6967490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700479-G-A

6967504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700468-A-G

6967565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700406-T-G

6967787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36700221-G-A

6969802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36699292-T-G

http://identifiers.org/hco/4/GRCh38#6969810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36699284-C-A

6970114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36698996-A-T

6970193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36698916-T-C

6970217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36698896-C-T

6971844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36697768-A-G

6971996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36697654-C-T

6972096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36697556-A-G

6973038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36697439-G-A

6974472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36696130-C-T

6974492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36696116-G-C

6986197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36688938-A-G

http://identifiers.org/hco/4/GRCh38#6986204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36688928-C-A

6986262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36688869-T-G

6986904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36688251-C-G

6986916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36688239-C-T

6987178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687933-G-T

6987186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36687925-T-C

6987201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687910-G-A

6987201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687910-G-T

6987315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687798-T-A

6987315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687798-T-C

http://identifiers.org/hco/4/GRCh38#6987316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36687797-C-A

6987316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687797-C-G

6987316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687797-C-T

6987322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36687791-G-A

6987322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36687791-G-C

6987322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36687791-G-T

http://identifiers.org/hco/4/GRCh38#6987494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36687637-C-A

6987494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36687637-C-T

6987509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36687622-T-G

http://identifiers.org/hco/4/GRCh38#6987694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36687430-C-A

6987694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36687430-C-T

6987772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36687386-C-G

6987772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36687386-C-T

6987851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36687318-C-T

6988216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36686979-G-A

6988216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36686979-G-T

6988223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36686972-C-G

6988223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36686972-C-T

6988322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36686885-A-G

6989413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685926-C-T

6989428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685896-G-A

6989434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685890-C-T

6989481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685836-G-C

6989486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685831-C-T

6989529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685781-C-T

6989557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685738-G-A

6989557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685738-G-C

http://identifiers.org/hco/4/GRCh38#6989583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36685683-C-A

6989724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36685557-C-T

http://identifiers.org/hco/4/GRCh38#6989837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36685454-C-A

6991025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36684722-C-T

6991279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36684398-A-T

6991977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683997-T-C

6992100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683873-G-T

6992168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683813-T-C

6992225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683751-G-T

6992563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683461-T-G

6993133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36683024-C-T

6993190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36682971-A-G

6993485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36682717-T-C

6994207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 36682367-A-G

http://identifiers.org/hco/4/GRCh38#6996442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36680251-C-A

http://identifiers.org/hco/4/GRCh38#6996447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36680246-C-A

6996447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36680246-C-T

6996581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36680102-C-T

6999174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36677814-A-G

http://identifiers.org/hco/4/GRCh38#6999208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36677780-A-C

6999208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36677780-A-T

6999243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36677746-T-C

6999847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36677298-T-C

http://identifiers.org/hco/4/GRCh38#7000907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676906-C-A

http://identifiers.org/hco/4/GRCh38#7001078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676791-A-C

7001078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36676791-A-G

7001078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36676791-A-T

7001266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676600-T-G

http://identifiers.org/hco/4/GRCh38#7001318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676543-C-A

http://identifiers.org/hco/4/GRCh38#7001319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676542-C-A

7001319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676542-C-G

7001319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676542-C-T

7001407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676461-G-A

7001407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676461-G-T

7001456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676415-A-G

7001472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36676375-A-G

7001503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676336-G-A

7001503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676336-G-C

7001503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676336-G-T

http://identifiers.org/hco/4/GRCh38#7001528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676310-C-A

7001543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676295-G-A

7001543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676295-G-T

http://identifiers.org/hco/4/GRCh38#7001554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36676275-C-A

7001554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676275-C-G

7001554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676275-C-T

7001578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676250-A-G

7001579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676249-G-A

7001579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676249-G-T

7001581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676247-T-C

7001594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676234-G-A

7001594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676234-G-T

7001599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36676229-T-C

7002302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36675444-T-C

7002429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36675301-G-C

7002992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36674812-T-A

7006468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36670049-C-G

7006576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669940-A-G

7006616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669904-T-G

http://identifiers.org/hco/4/GRCh38#7006787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36669743-C-A

7006817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669711-T-G

http://identifiers.org/hco/4/GRCh38#7006819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36669709-C-A

7006819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669709-C-G

7006825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669703-T-C

7006832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669696-G-A

7007470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36669170-C-G

7007588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, missense_variant
orthologous variants: 36668102-A-G

7007618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, stop_gained
orthologous variants: 36668070-G-A

7007618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, missense_variant
orthologous variants: 36668070-G-C

7007639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36668050-G-C

7007688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36668002-G-A

7007688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36668002-G-C

http://identifiers.org/hco/4/GRCh38#7007713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36667975-C-A

7007713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36667975-C-G

7007713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36667975-C-T

7007727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36667969-G-A

7007727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36667969-G-C

7007727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36667969-G-T

7008235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron_variant, undefined
orthologous variants: 36667522-G-A

7009228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36666392-G-T

7009330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36666296-A-G

7009373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36666247-G-A

7009611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36666046-G-A

7009740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665912-G-A

7009740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665912-G-T

7010031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665617-G-A

7010031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665617-G-C

7010031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665617-G-T

7010503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665199-G-A

7010503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665199-G-T

7010581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36665114-T-C

7010755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 36664946-G-A

7010816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664888-T-C

http://identifiers.org/hco/4/GRCh38#7010866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36664837-A-C

7010888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664819-G-A

7010888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664819-G-C

7011291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664521-C-T

7011377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664441-C-G

7011382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664436-C-T

7011402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664417-A-G

7011439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664382-C-T

7011539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664297-T-G

7011549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36664287-T-G

7014398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36662529-T-G

7014508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36662416-G-A

7014508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36662416-G-T

7015001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36661967-G-A

7017799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36660048-T-C

7018593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36659504-G-A

7018935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36659186-G-A

7020912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36658367-G-A

7020912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36658367-G-T

7021101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36658210-A-G

7021118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36658179-C-T

http://identifiers.org/hco/4/GRCh38#7021198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36658097-A-C

7021198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36658097-A-G

7021942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36657708-C-G

7021942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36657708-C-T

7021997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36657655-T-C

7022019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36657634-C-T

7024833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652746-C-T

http://identifiers.org/hco/4/GRCh38#7024857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36652724-C-A

7024857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652724-C-G

7024857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652724-C-T

http://identifiers.org/hco/4/GRCh38#7024872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36652709-C-A

7024872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652709-C-G

7024925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652680-G-A

7024925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36652680-G-C

7025020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652602-A-T

7025053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652569-A-G

7025086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652536-T-G

7025102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652520-C-T

7025194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652428-C-T

7025196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652426-C-G

7025196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652426-C-T

7025199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652423-C-T

7025203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652419-G-A

7025205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652417-G-T

7025226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652396-G-A

7025226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652396-G-C

7025238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36652384-G-A

7025240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36652382-G-A

7029177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36651098-C-G

7029232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36651043-T-G

7029475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36650824-C-G

7030228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36650537-G-A

7030228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36650537-G-T

http://identifiers.org/hco/4/GRCh38#7030266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650513-C-A

7030266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: intron variant
orthologous variants: 36650513-C-T

7030330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36650453-C-T

7030332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36650451-G-C

7030332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36650451-G-T

7030353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36650430-C-T

7030354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36650429-C-G

7030354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: missense variant
orthologous variants: 36650429-C-T

7030356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: synonymous variant
orthologous variants: 36650427-G-C

7030400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650384-G-T

7030409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650372-C-T

7030449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650335-T-A

7030449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650335-T-C

7030449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650335-T-G

7030456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650328-T-C

7030456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650328-T-G

http://identifiers.org/hco/4/GRCh38#7030477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650311-C-A

7030477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650311-C-G

7030477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650311-C-T

7030498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650288-A-G

http://identifiers.org/hco/4/GRCh38#7030508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650278-C-A

7030508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3 prime UTR variant
orthologous variants: 36650278-C-G

http://identifiers.org/hco/4/GRCh38#7030556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650247-A-C

7030560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650243-T-A

7030561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650242-T-A

7030592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650211-G-C

http://identifiers.org/hco/4/GRCh38#7030619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650184-C-A

7030619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650184-C-T

http://identifiers.org/hco/4/GRCh38#7030670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36650133-A-C

7030670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650133-A-T

7030683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650120-A-G

7030714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36650089-T-C

7030814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649992-T-G

7030856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649954-A-G

http://identifiers.org/hco/4/GRCh38#7030875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649936-C-A

7030875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649936-C-T

http://identifiers.org/hco/4/GRCh38#7030886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649926-C-A

7030890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649922-G-A

7030890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649922-G-T

7030913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649901-G-A

7030913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649901-G-T

http://identifiers.org/hco/4/GRCh38#7030920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649894-C-A

7030981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649834-G-A

7030981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649834-G-T

http://identifiers.org/hco/4/GRCh38#7031043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649772-C-A

7031065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649761-G-T

7031099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649730-A-G

7031146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649691-G-T

http://identifiers.org/hco/4/GRCh38#7031152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649685-C-A

7031152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649685-C-T

7031208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649664-G-A

7031208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649664-G-T

7031295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649574-G-A

7031295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649574-G-T

7031321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649546-C-G

7031321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649546-C-T

7031325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649542-G-A

7031325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649542-G-T

7031337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649530-T-C

7031338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649529-G-A

7031338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649529-G-T

7031348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649519-A-G

http://identifiers.org/hco/4/GRCh38#7031403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649461-C-A

7031405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649459-T-A

7031410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649454-C-T

7031426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649440-G-A

7031426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649440-G-T

7031472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649423-T-C

http://identifiers.org/hco/4/GRCh38#7031473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649422-C-A

7031479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649416-G-A

7031540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649350-G-T

7031625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649274-G-T

7031656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649243-G-A

7031670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649229-T-C

http://identifiers.org/hco/4/GRCh38#7031719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649192-C-A

http://identifiers.org/hco/4/GRCh38#7031733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649178-C-A

7031733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649178-C-T

7031744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649165-G-A

7031763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649146-T-C

7031763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649146-T-G

7031769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649140-G-A

7031769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649140-G-T

7031791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649118-A-G

http://identifiers.org/hco/4/GRCh38#7031804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649105-C-A

7031804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649105-C-T

7031805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649104-C-G

7031805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649104-C-T

7031816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649100-T-C

http://identifiers.org/hco/4/GRCh38#7031824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649092-C-A

7031836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649078-G-A

7031836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649078-G-C

7031836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649078-G-T

http://identifiers.org/hco/4/GRCh38#7031837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36649077-C-A

7031837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649077-C-T

7031856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649052-T-C

7031876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649037-G-T

7031877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649036-G-T

7031885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649028-G-A

7031885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649028-G-T

7031894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649019-G-A

7031894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36649019-G-T

7031944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648978-C-T

7031958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648964-G-A

7031958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648964-G-T

7031969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648954-G-A

7031969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648954-G-T

7031976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648947-G-A

7031976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648947-G-T

http://identifiers.org/hco/4/GRCh38#7031977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648946-C-A

7031977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648946-C-T

7031998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648936-G-A

7031998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648936-G-T

http://identifiers.org/hco/4/GRCh38#7032004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648930-C-A

7032004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648930-C-T

7032006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648928-T-C

7032023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648912-G-T

http://identifiers.org/hco/4/GRCh38#7032032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648903-C-A

http://identifiers.org/hco/4/GRCh38#7032034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648901-C-A

7032034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648901-C-G

7032034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648901-C-T

http://identifiers.org/hco/4/GRCh38#7032082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648855-C-A

7032082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648855-C-T

7032083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648854-A-G

7032107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648830-G-A

7032124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648814-T-C

http://identifiers.org/hco/4/GRCh38#7032148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648794-C-A

7032148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648794-C-T

7032205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648743-A-G

7032216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648732-A-G

7032241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648707-G-T

7032337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648609-T-G

http://identifiers.org/hco/4/GRCh38#7032367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648579-C-A

7032367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648579-C-T

7032369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648577-T-C

7032384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648562-G-A

7032384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648562-G-T

7032389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648557-A-G

http://identifiers.org/hco/4/GRCh38#7032461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648485-C-A

7032523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648443-A-G

7032523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648443-A-T

7032551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648417-C-T

7032593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36648374-G-C

7032641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648336-A-G

7032647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648330-A-G

http://identifiers.org/hco/4/GRCh38#7032648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648329-A-C

7032760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648266-G-T

http://identifiers.org/hco/4/GRCh38#7032764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648262-C-A

7032764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648262-C-T

http://identifiers.org/hco/4/GRCh38#7032798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#36648228-C-A

7032798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648228-C-T

7032826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648202-G-T

7032843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648192-C-T

7032867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648168-G-T

7032878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648167-C-G

7032896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648148-T-C

7032899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29246
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36648145-G-T