110305943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11361585-G-T

110306055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361695-G-C

110306055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361695-G-T

110306058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361698-G-C

110306073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361711-G-A

110306207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361822-T-C

110306633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362209-G-A

110306633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362209-G-C

http://identifiers.org/hco/13/GRCh38#110306856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11362421-C-A

110306856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362421-C-T

110306868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362437-G-A

110306868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362437-G-T

110306930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11362502-G-T

110307073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362665-G-A

110307073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362665-G-T

110307077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362669-G-A

110307077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362669-G-T

110307457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363049-C-T

110307466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363058-G-A

110307466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363058-G-C

110307466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363058-G-T

110307488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363080-G-A

110307488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11363080-G-T

110307545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363131-A-G

110307551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363137-G-A

110307551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363137-G-T

http://identifiers.org/hco/13/GRCh38#110307583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11363169-A-C

110307583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363169-A-G

110307603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363188-G-T

110307607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363192-C-T

http://identifiers.org/hco/13/GRCh38#110307611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11363196-C-A

110307614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363199-T-C

110307728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363300-G-A

110307728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363300-G-T

110307749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363320-G-A

110307749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363320-G-C

110307749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363320-G-T

110307926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11363486-T-C

110307937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11363497-G-A

110308084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11363645-G-T

110308224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363792-T-A

110308224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363792-T-G

110308275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363830-T-A

110308279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363834-C-T

110308353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363859-C-T

110308449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363945-G-A

110308657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364137-G-C

110308990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364454-G-C

110309011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364459-C-T

110309012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364460-G-A

110309012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364460-G-T

110309020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364468-G-C

110309234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364638-C-T

110312139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366388-G-A

110312305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366545-C-T

110312467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366716-T-C

110312636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366821-G-C

110312668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11366853-T-C

110312670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366855-C-T

110312676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366861-G-T

110312763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11366936-A-G

110312996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367139-G-A

110312996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367139-G-C

110313125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367411-G-A

110313225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367454-G-A

110313291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367503-G-C

110313441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367654-G-A

110313441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367654-G-C

110315723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11370084-G-A

110315738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11370099-C-T

110315818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11370144-G-A

110315883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11370219-C-T

110315980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11370325-C-T

110319488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11372624-T-C

110319821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11372891-C-T

110320176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11373195-G-A

110320441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11373398-C-T

110320463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11373420-C-G

110323523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11374636-T-G

110323658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11374749-A-G

110323669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11374762-C-T

110323759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11374843-G-A

110323998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11375062-C-T

110324170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11375231-A-G

110324361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11375986-G-A

110324659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11376264-G-T

110325007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11376503-C-T

http://identifiers.org/hco/13/GRCh38#110325014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11376510-C-A

110325099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11376563-G-A

110325251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11376711-G-A

110325478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11376935-A-G

110325711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11377161-T-C

110325714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11377164-A-G

110325782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11377224-G-A

110325782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11377224-G-C

110327611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11378172-G-C

110327708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11378260-C-G

110327802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11378347-A-G

110327890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11378420-A-G

110328369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 11379403-G-A

110328477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11379496-G-A

110328477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11379496-G-T

110328523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11379535-T-C

110328538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11379550-G-A

http://identifiers.org/hco/13/GRCh38#110328616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11379625-C-A

110328616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11379625-C-T

110328897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11379857-G-A

http://identifiers.org/hco/13/GRCh38#110328905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11379865-C-A

110328980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11379938-T-C

110329189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380161-G-A

110329335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380289-A-G

110329694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380446-A-G

110329863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380607-C-G

110329863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380607-C-T

110329955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11380977-G-T

110330080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381095-A-G

110330165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381179-C-T

110330607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381618-C-T

110330681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381675-C-T

110330682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381676-G-A

110330985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11381948-C-T

110331170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11382254-T-C

110331234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11382328-T-C

110331285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11382401-T-C

110331412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11382540-G-A

110331453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11382592-C-T

http://identifiers.org/hco/13/GRCh38#110332591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11383705-A-C

110332870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11383971-G-A

110332972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384076-G-A

110333465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384397-C-T

110333514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384428-T-A

110333624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384537-G-A

110333626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384538-G-A

110333846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384726-G-A

110333846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384726-G-T

110333896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384776-T-C

110334123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11384958-T-C

http://identifiers.org/hco/13/GRCh38#110334606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11385319-C-A

110334613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11385322-G-T

110334720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11385427-A-G

110334727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11385434-A-G

110334754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11385461-C-T

http://identifiers.org/hco/13/GRCh38#110334755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11385462-A-C

110334755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11385462-A-G

110335858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386000-A-G

110335960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386081-C-T

110336008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386128-C-T

110336013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386133-T-C

110336316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386417-G-A

110336387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386487-C-G

110336387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11386487-C-T

110339175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11388559-C-G

110341010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11390414-T-C

http://identifiers.org/hco/13/GRCh38#110341117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11390521-C-A

110341117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11390521-C-T

110341130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11390532-T-C

110341130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11390532-T-G

110341541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391045-G-A

110341887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391409-G-A

110341965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391483-A-G

110342062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391565-C-T

110342366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391843-C-T

110342457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11391954-G-A

110342758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11392189-C-T

110342789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11392214-A-G

110342890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11392297-A-G

110342947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11392352-T-C

110343067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11392475-G-T

110343449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11393058-T-C

110343449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11393058-T-G

110343454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11393062-G-A

110343638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11393228-A-G

http://identifiers.org/hco/13/GRCh38#110343972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11393572-C-A

110344277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11393844-G-A

110344447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11393999-A-G

110344498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394047-T-C

110344498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394047-T-G

110344950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394429-G-A

110345071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394536-G-A

110345113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394580-G-A

110345170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394623-A-G

110345183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394631-A-G

http://identifiers.org/hco/13/GRCh38#110345332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11394776-C-A

110345332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394776-C-T

110345404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11394834-G-T

110345979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11395234-G-A

110346096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11395324-A-G

110346252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11395426-A-G

110347033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11396691-G-C

110347033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11396691-G-T

110347037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11396695-G-A

110347184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11396839-C-G

110347385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397050-A-G

110347575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397162-C-T

110347624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397184-T-C

110347838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397369-C-T

110347881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397386-T-C

110347941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397425-C-T

110348042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11397514-A-G

110349067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398456-T-C

110349152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398543-C-T

110349236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398612-A-G

110349275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398641-T-G

110349346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398689-A-G

110349376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398721-C-T

110349399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11398745-G-A

110350357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11399359-C-T

110350451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11399420-C-T

110350575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11399543-G-A

110350601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11399573-C-T

110350875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11399797-A-G

110352484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400522-C-G

110352484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400522-C-T

110352561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400689-T-A

110352561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400689-T-G

110352679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400789-C-T

110352811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11400894-G-A

http://identifiers.org/hco/13/GRCh38#110352906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11400982-C-A

110352965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401020-C-T

110353227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401144-G-C

110353308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401217-G-A

110353341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401248-A-G

110353418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401320-G-T

110353487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401385-A-G

110353586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401485-G-A

110353586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401485-G-C

http://identifiers.org/hco/13/GRCh38#110353858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11401716-C-A

110353910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401743-A-G

110354020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401786-A-G

110354103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11401870-G-A

110354575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11402517-C-G

110354639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11402565-A-G

110354639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11402565-A-T

110356287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11403648-C-G

110356287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11403648-C-T

110356305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11403666-C-G

110356305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11403666-C-T

http://identifiers.org/hco/13/GRCh38#110356316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11403682-A-C

110356316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11403682-A-G

110357461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11404266-T-A

110357461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11404266-T-C

110357537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11404342-T-A

110357537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11404342-T-C

110357537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11404342-T-G

110357562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant
orthologous variants: 11404366-A-G

110357578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant
orthologous variants: 11404380-A-G

110358990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11404817-A-G

110359092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11404933-A-G

110359213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11405056-T-C

110359233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11405069-T-C

110359254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11405095-A-G

110359506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406097-G-A

110359733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406295-G-A

110359754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406316-C-T

110359948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406453-G-A

110360120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406817-G-T

110360121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406818-A-G

110360121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406818-A-T

110360137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11406852-C-T

110360360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407070-T-C

http://identifiers.org/hco/13/GRCh38#110360467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11407166-C-A

110360484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11407183-T-C

110360679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407324-G-A

http://identifiers.org/hco/13/GRCh38#110361101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11407623-A-C

110361155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407680-G-A

110361261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407771-G-A

110361377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407885-G-A

110361377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11407885-G-T

110361811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11408297-G-T

110361840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11408314-C-G

110361840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11408314-C-T

110364781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11410837-C-T

110366542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11413161-G-A

110366666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11413273-T-A

110366909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11413483-A-G

110366914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11413488-T-G

110367395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11413942-T-C

http://identifiers.org/hco/13/GRCh38#110367542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11414071-A-C

110367610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414125-G-A

110367721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414212-C-T

110367872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414341-C-T

110368002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414480-G-C

110368002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414480-G-T

110368081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414664-C-G

110368081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414664-C-T

110368082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414665-G-A

110368130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414710-G-A

110368189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414768-C-G

110368237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414819-G-A

110368305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11414887-G-T

110370704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11415863-T-C

110370725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11415882-T-C

110370907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11416176-G-A

110370989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11416257-T-C

110371008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11416275-A-G

110371789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11416910-G-A

110372101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417198-A-G

110372184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417288-C-T

110372204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417308-G-A

110372251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417355-C-G

110372437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417501-T-C

110372444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417508-T-C

http://identifiers.org/hco/13/GRCh38#110372447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11417510-C-A

110372619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417665-C-T

110372834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11417897-G-A

110373179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418273-G-A

110373202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418296-C-G

110373425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418504-G-T

110373667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418734-A-G

110373673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418740-A-G

110373850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418876-G-A

110373994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11418962-G-C

110374055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419021-G-A

110374055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419021-G-C

110374124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419071-A-G

110374284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419195-G-A

110374386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419284-T-C

110374387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419285-G-A

110374480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419377-A-G

http://identifiers.org/hco/13/GRCh38#110374514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11419396-A-C

110374652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419509-A-G

110375074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419892-A-G

110375170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11419980-T-C

110375279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11420086-G-C

110375295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11420102-A-G

110380260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11420964-T-C

110380306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11421010-C-T

http://identifiers.org/hco/13/GRCh38#110381783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11421748-C-A

110381783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11421748-C-T

110381846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11421788-G-A

http://identifiers.org/hco/13/GRCh38#110381979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11421873-A-C

http://identifiers.org/hco/13/GRCh38#110382352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11422177-C-A

110382352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11422177-C-T

110382626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11422467-C-G

110382699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11422539-A-T

110383219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423009-A-G

110383250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423038-G-A

110383274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423066-G-A

110383345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423138-T-C

110383351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423146-G-A

110383583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11423364-G-T

110387337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424477-T-C

110387474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424595-T-C

110387580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424703-C-G

110387613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424735-C-T

110387653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424775-C-T

110387737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424866-A-G

110387785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424914-C-T

110387800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424947-G-A

http://identifiers.org/hco/13/GRCh38#110387846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11424988-C-A

110387846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424988-C-T

110387847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424989-G-A

110387847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424989-G-T

110387850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11424992-G-T

110388008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11425149-C-T

http://identifiers.org/hco/13/GRCh38#110388994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11426456-C-A

110389070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11426523-T-C

110389097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11426550-G-A

110389679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427026-A-G

110389893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427280-A-G

110389893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427280-A-T

110389900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427302-C-T

110390117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427490-T-G

110390526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427826-C-T

110390634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11427943-A-T

110390854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428153-G-A

110391085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428370-G-A

110391177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428464-G-T

110391178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428465-C-T

110391287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428544-C-T

110391650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11428762-T-C

http://identifiers.org/hco/13/GRCh38#110391918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11429041-A-C

110392721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11429834-G-T

110393226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430302-C-G

110393226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430302-C-T

110393413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430412-A-G

110393421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430419-G-A

110393435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430433-T-C

110393436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430434-A-G

110393466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11430467-A-G

110395243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11431500-A-G

110396645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11432179-T-C

110396741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11432265-T-A

110397339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11432811-A-G

110397395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11432875-A-G

110397465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11433006-G-C

110397712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11433247-T-G

110397948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11433482-G-C

110397990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11433522-G-A

http://identifiers.org/hco/13/GRCh38#110398789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11433830-C-A

110398835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11433866-C-T

http://identifiers.org/hco/13/GRCh38#110398910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11433938-C-A

110398971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11434012-C-T

110399155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11434200-T-C

110399200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11434239-C-T

http://identifiers.org/hco/13/GRCh38#110399437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11434473-C-A

110399625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11434652-C-T

110399674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11434704-G-T

110400084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435102-T-C

110400538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435322-G-T

110400649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435428-A-G

110400936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435644-T-G

110400980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435692-G-T

110400999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435711-A-G

110401270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11435931-G-T

110405972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11437453-C-T

110406231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11437694-G-T

http://identifiers.org/hco/13/GRCh38#110406334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11437780-C-A

110406381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11437825-C-G

110406387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11437831-G-C

110406575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11437991-A-G

http://identifiers.org/hco/13/GRCh38#110406705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11438090-A-C

110407069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11438919-A-G

110407096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11438949-A-G

110407098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11438951-C-G

110408348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11439850-G-T

110408593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440053-G-A

110408593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440053-G-T

110408603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440058-C-T

110408620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440074-C-T

http://identifiers.org/hco/13/GRCh38#110408741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11440159-A-C

110408787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440200-G-A

110408787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11440200-G-T

http://identifiers.org/hco/13/GRCh38#110409729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11441194-A-C

110409729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441194-A-G

110409771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441237-G-A

110409804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441261-G-C

110409897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441339-A-G

110409901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441343-G-T

110409946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11441387-G-A

http://identifiers.org/hco/13/GRCh38#110410354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11442073-C-A

110410354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11442073-C-T

110412017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11442610-G-A

110412071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11442667-G-A

110412077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11442673-C-T

110412296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11442866-G-A

110412387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11442957-C-T

110412670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11443187-T-C

110412760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11443286-G-A

110412760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11443286-G-T

110412966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11443479-G-C

110412969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11443482-C-T

110418975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444720-A-G

110418975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444720-A-T

110418994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444739-T-C

http://identifiers.org/hco/13/GRCh38#110419045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11444790-C-A

110419164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444878-A-G

110419180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444890-C-T

110419215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11444925-C-T

110419304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445005-T-C

110419339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445037-C-T

110419537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445114-G-A

110419567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445142-G-A

110419803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445354-G-A

110419989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445521-G-A

110420004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445536-T-G

110420028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445556-A-G

110420129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445662-G-A

110420129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445662-G-T

http://identifiers.org/hco/13/GRCh38#110420150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11445680-A-C

110420266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445779-T-C

110420367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11445853-T-C

110420547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11446062-T-C

110420663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11446170-C-T

110420768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11446262-A-T

110420988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11446466-T-A

http://identifiers.org/hco/13/GRCh38#110421045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11446496-C-A

110421245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11446823-A-T

110421475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447106-A-G

http://identifiers.org/hco/13/GRCh38#110421587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11447225-A-C

110421820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447409-G-A

110421866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447450-T-A

110421870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447454-G-T

110422115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447617-A-T

110422488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11447926-T-G

110424594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11448543-G-A

110424594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11448543-G-T

110424656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11448590-G-A

110424656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11448590-G-T

110424784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11448712-A-G

110424912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11449665-G-A

http://identifiers.org/hco/13/GRCh38#110424958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11449709-A-C

110424958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11449709-A-G

110424958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11449709-A-T

http://identifiers.org/hco/13/GRCh38#110425042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11449792-C-A

110425042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11449792-C-T

110425153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11449906-G-A

110425496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450363-A-T

110425599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11450444-A-T

110425628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450474-G-A

110425628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450474-G-C

110425628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450474-G-T

110425768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450597-G-A

110425986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450768-G-A

110428302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11450997-C-G

110428367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11451061-G-A

110428368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11451062-G-T

http://identifiers.org/hco/13/GRCh38#110428412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451108-C-A

110428440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11451122-T-C

110428526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11451207-C-G

110428526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11451207-C-T

110428536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11451217-T-C

http://identifiers.org/hco/13/GRCh38#110428594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451275-C-A

110428594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant
orthologous variants: 11451275-C-T

http://identifiers.org/hco/13/GRCh38#110428821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451547-C-A

110428821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451547-C-T

110428828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451554-T-G

http://identifiers.org/hco/13/GRCh38#110428835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451561-A-C

110428882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451604-G-T

110428952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451683-A-G

110428986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451728-T-C

110428998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451740-G-T

110429001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451743-A-T

http://identifiers.org/hco/13/GRCh38#110429012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451754-A-C

110429106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451815-A-G

110429106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451815-A-T

110429175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451876-T-A

http://identifiers.org/hco/13/GRCh38#110429257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451924-A-C

110429257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451924-A-T

http://identifiers.org/hco/13/GRCh38#110429258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11451925-C-A

110429258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451925-C-T

110429272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451954-T-G

110429278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451960-T-A

110429278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451960-T-C

110429278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451960-T-G

110429283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451965-T-G

110429286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451968-G-A

110429286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451968-G-C

110429286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451968-G-T

110429301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451983-T-A

110429301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451983-T-C

110429301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11451983-T-G

110429870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11452147-A-G

110429870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11452147-A-T

110429876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11452153-G-A

http://identifiers.org/hco/13/GRCh38#110429954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11452232-C-A

110429954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 11452232-C-T

http://identifiers.org/hco/13/GRCh38#110430080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11452355-C-A

110430080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11452355-C-T

110430087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11452362-A-G

110430439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11453022-A-G

110430658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453447-C-T

110430661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453450-C-T

110430938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453578-C-G

110430938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453578-C-T

http://identifiers.org/hco/13/GRCh38#110430940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11453580-C-A

110430943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453584-A-G

110430949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453590-A-G

110430961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453602-T-C

110430961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453602-T-G

110430989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453629-T-G

110430995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453635-G-A

110430995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11453635-G-T

http://identifiers.org/hco/13/GRCh38#110431117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11453709-C-A

110431401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454051-G-A

110431477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454139-C-G

110431477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454139-C-T

110431511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454174-C-G

110431557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454246-C-T

110431953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454609-C-T

110431968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454620-G-A

http://identifiers.org/hco/13/GRCh38#110432212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11454849-C-A

110432288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454924-A-G

110432308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11454947-T-C

110432385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455020-A-G

110432387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455022-G-A

110432399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455030-T-C

110432457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455085-A-G

110432546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455166-C-T

110432563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455186-G-T

110432632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11455246-A-T

110432639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11455255-A-G

110432646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11455262-C-G

110432646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11455262-C-T

110432747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455360-C-T

110432870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455475-G-T

110433047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455613-G-A

110433087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455652-T-G

110433202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455774-G-T

110433224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11455803-G-A

http://identifiers.org/hco/13/GRCh38#110433294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11455883-C-A

110433602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456168-G-A

110433949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456462-C-T

110434100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456570-G-T

http://identifiers.org/hco/13/GRCh38#110434313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11456721-C-A

110434313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456721-C-G

110434313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456721-C-T

110434424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11456836-C-T

110434526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456889-G-A

110434553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456904-C-G

110434569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456918-T-C

110434658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11456998-T-A

110434725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457065-A-G

110435382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457332-A-G

110435550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457473-A-G

110435739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457640-T-G

110435853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457720-G-A

http://identifiers.org/hco/13/GRCh38#110436052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11457832-A-C

110436052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457832-A-G

http://identifiers.org/hco/13/GRCh38#110436074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11457854-C-A

110436074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457854-C-T

110436078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457858-T-C

110436101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457878-A-G

110436101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457878-A-T

110436108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457885-G-C

110436108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11457885-G-T

110436313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11458096-C-G

110436354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11458131-C-T

110436406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458176-A-T

110436439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458211-T-C

110436495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458267-T-A

110436495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458267-T-C

http://identifiers.org/hco/13/GRCh38#110436501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11458272-C-A

110436501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458272-C-G

110437873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458751-T-A

http://identifiers.org/hco/13/GRCh38#110437921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11458801-C-A

110437921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458801-C-T

110437940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458820-G-A

110437940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458820-G-T

http://identifiers.org/hco/13/GRCh38#110437956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11458836-C-A

110437956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458836-C-T

110437969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458849-A-G

110437975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458855-G-A

110437975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458855-G-C

110437975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458855-G-T

110437987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458867-T-A

110438052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458932-G-A

110438073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458954-G-A

110438076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458957-C-T

110438078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458959-T-A

110438078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458959-T-G

110438103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11458984-T-C

http://identifiers.org/hco/13/GRCh38#110438124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11459005-C-A

110438124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459005-C-T

http://identifiers.org/hco/13/GRCh38#110438166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11459037-C-A

110438166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459037-C-G

110438195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459058-T-A

110438195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459058-T-G

110438281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459119-A-G

110438291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459131-C-T

110438322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459163-C-T

110438359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459194-C-T

110438374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459209-C-G

110438378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459213-C-G

110438424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459231-G-A

110438424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459231-G-T

110438426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459233-G-A

110438426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459233-G-T

110438440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459249-G-C

http://identifiers.org/hco/13/GRCh38#110438488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11459283-A-C

110438499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459294-G-A

110438516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459304-G-A

110438548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459356-A-G

110438548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459356-A-T

110438579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459384-C-G

110438588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459392-G-A

110438611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11459415-C-T

110438677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459481-C-T

110438735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459545-T-A

110438775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459585-T-A

110438775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459585-T-C

110438777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459587-T-A

110438777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459587-T-C

110438793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459598-T-C

110438793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459598-T-G

http://identifiers.org/hco/13/GRCh38#110438820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11459625-A-C

110438820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459625-A-G

110438820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459625-A-T

110438858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459657-G-T

110438926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459715-C-G

110438926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459715-C-T

http://identifiers.org/hco/13/GRCh38#110439083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11459844-A-C

110439083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459844-A-G

110439089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11459859-C-T

http://identifiers.org/hco/13/GRCh38#110439815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11460081-A-C

110439815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11460081-A-G

http://identifiers.org/hco/13/GRCh38#110439822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11460088-C-A

110439822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11460088-C-G

110439822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11460088-C-T

110439848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460114-T-A

110439848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460114-T-C

110439849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460115-G-A

110439849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460115-G-C

http://identifiers.org/hco/13/GRCh38#110439931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11460179-C-A

110439931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460179-C-T

110439940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460185-A-T

110439943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460188-A-G

110439943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460188-A-T

110439945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460190-T-A

110439945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460190-T-G

110440033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460282-A-G

110440037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460286-A-T

110440890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11460772-A-G

110441172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461032-A-G

110441185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461046-A-G

110441221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461085-C-G

110441285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461123-A-G

110441586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461375-A-G

110442259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461765-T-C

110442292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461789-A-G

110442378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11461879-G-A

110442603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11462083-A-G

110442659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11462185-T-C

110442756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11462269-T-C

http://identifiers.org/hco/13/GRCh38#110444703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11463053-A-C

110444713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11463063-T-A

http://identifiers.org/hco/13/GRCh38#110445822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11463972-C-A

110445822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11463972-C-G

110445979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464065-G-A

110445979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464065-G-T

http://identifiers.org/hco/13/GRCh38#110445980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11464066-C-A

110445980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464066-C-T

110446022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464078-T-A

110446022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464078-T-G

110446376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464341-G-A

110446377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464342-C-T

110446442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464403-G-A

110446445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464406-C-T

110446453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464414-C-T

110446569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464543-C-T

http://identifiers.org/hco/13/GRCh38#110446709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11464678-C-A

110446709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11464678-C-T

110446827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11464771-A-G

110446884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464828-T-A

110446884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464828-T-C

110446884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464828-T-G

110446892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464836-T-G

110446923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464863-G-A

110446923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464863-G-T

110446953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464893-T-C

110446953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11464893-T-G

110449661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465346-G-A

110449661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465346-G-T

110449662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465347-A-T

110449740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11465425-A-T

110449753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11465438-C-T

http://identifiers.org/hco/13/GRCh38#110449779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11465464-C-A

110449779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11465464-C-G

110449779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11465464-C-T

110449798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465483-G-C

110449798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465483-G-T

110449834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465507-G-A

110449834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465507-G-C

110449834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465507-G-T

http://identifiers.org/hco/13/GRCh38#110449844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11465517-C-A

110449844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465517-C-G

http://identifiers.org/hco/13/GRCh38#110449864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11465534-C-A

110449864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465534-C-T

110449872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465542-A-T

110449976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465617-A-T

110450075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465724-G-A

110450159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465787-A-G

110450161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465789-T-A

110450161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11465789-T-C

http://identifiers.org/hco/13/GRCh38#110450229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11465850-C-A

110450359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11465980-C-T

110450380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11466001-G-A

110450396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11466017-T-C

110450429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11466050-G-A

110450438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11466059-A-G

110450447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11466068-A-G

http://identifiers.org/hco/13/GRCh38#110450564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11466128-A-C

110450773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11466274-A-G

110450842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11466317-G-A

110450909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11466362-T-A

110450909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11466362-T-G

110451038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11466475-T-C

110453723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11467594-A-G

110453871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11467763-G-A

110454104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11467998-C-G

110454104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11467998-C-T

110454251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468077-C-T

http://identifiers.org/hco/13/GRCh38#110454442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11468252-C-A

110454442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468252-C-T

110454501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468322-A-G

110454578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468390-G-A

110454602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468406-C-T

110454609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468412-C-T

110454707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468518-G-A

http://identifiers.org/hco/13/GRCh38#110454901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11468673-C-A

http://identifiers.org/hco/13/GRCh38#110454902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11468674-C-A

110454912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468684-C-T

110454916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468688-C-G

110454921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468693-T-A

110454942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468714-C-G

110454942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11468714-C-T

110455230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469060-G-A

http://identifiers.org/hco/13/GRCh38#110455282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11469121-A-C

http://identifiers.org/hco/13/GRCh38#110455557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11469359-A-C

110455652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469443-G-A

110455727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469518-C-G

110455767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469555-G-A

110455790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469572-T-G

110455791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469573-G-A

110455843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11469602-T-A

110455866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11469633-C-T

110456012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11469814-C-T

110456205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11470011-G-A

110456210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, undefined
orthologous variants: 11470016-T-C

110456414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470258-A-T

110456415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470259-G-A

110456415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470259-G-T

110456441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470284-G-A

110456441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470284-G-T

110456442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470285-T-A

110456536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470369-T-A

110456536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470369-T-C

110456536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470369-T-G

110456541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470374-G-C

110456541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470374-G-T

110456592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470424-T-C

http://identifiers.org/hco/13/GRCh38#110456607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11470439-C-A

110456607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470439-C-T

110456647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470466-T-C

110456647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470466-T-G

110456652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470471-T-G

110457314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11470548-A-G

110457335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 11470569-C-T

http://identifiers.org/hco/13/GRCh38#110457463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11470701-A-C

110457463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11470701-A-G

110457496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11470736-A-G

http://identifiers.org/hco/13/GRCh38#110458684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11471086-C-A

110458684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471086-C-G

110458697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471099-C-T

http://identifiers.org/hco/13/GRCh38#110458700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11471102-C-A

110458700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471102-C-G

110458700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471102-C-T

110458744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471140-G-T

110458751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11471147-C-T

110458862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11471250-C-T

110460563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11472204-G-A

110460563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11472204-G-C

110460847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11472790-T-C

http://identifiers.org/hco/13/GRCh38#110461042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11472987-A-C

110462128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11473566-C-G

110462128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11473566-C-T

110462208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11473645-C-G

110462208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11473645-C-T

110462216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11473653-G-A

110462273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11473712-T-C

110462443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11473884-A-G

110462443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11473884-A-T

110462541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11473964-A-G

110462569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11473991-A-G

110465364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475300-A-G

http://identifiers.org/hco/13/GRCh38#110465389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475323-C-A

110465389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475323-C-G

110465407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 11475341-T-C

110465482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11475416-G-T

110465509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11475443-C-T

http://identifiers.org/hco/13/GRCh38#110465730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475683-C-A

110465730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475683-C-T

http://identifiers.org/hco/13/GRCh38#110465744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475700-C-A

110465744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475700-C-T

110465752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475703-T-A

http://identifiers.org/hco/13/GRCh38#110465882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475800-C-A

110465882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475800-C-G

110465882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475800-C-T

http://identifiers.org/hco/13/GRCh38#110465887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475805-C-A

110465887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475805-C-T

http://identifiers.org/hco/13/GRCh38#110465902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11475825-A-C

110465902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475825-A-G

110465931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11475859-A-G

110466013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11475939-A-G

110466038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11475964-G-A

110466350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476340-G-A

110466666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476655-C-T

110466668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476657-A-G

110466668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476657-A-T

110466739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476724-C-G

110466739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476724-C-T

110466740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476725-G-A

110466799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476774-A-T

110466858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476829-A-G

110467017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476984-T-C

110467021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11476988-T-C

http://identifiers.org/hco/13/GRCh38#110467081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11477048-C-A

110467081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11477048-C-T

110469091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477429-G-A

110469091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477429-G-T

http://identifiers.org/hco/13/GRCh38#110469105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11477440-C-A

110469105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477440-C-G

110469202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477538-T-C

http://identifiers.org/hco/13/GRCh38#110469273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11477609-C-A

110469273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense variant
orthologous variants: 11477609-C-T

110469317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11477653-A-G

110469359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477688-G-A

110469359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477688-G-T

110469440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477773-T-C

110469452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11477785-G-T

http://identifiers.org/hco/13/GRCh38#110469538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11477844-C-A

110472780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11479169-A-G

110472790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11479175-G-A

110472790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11479175-G-T

110473074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: synonymous variant
orthologous variants: 11479452-A-G

110473243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron variant
orthologous variants: 11479624-A-G

110477941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11481195-A-G

110478019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481256-T-C

110478031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481268-G-A

110478031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481268-G-T

110478109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481346-A-G

110478127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481364-G-A

110478130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11481367-G-T

110478197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481440-G-A

110478197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481440-G-T

110478203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481446-A-G

http://identifiers.org/hco/13/GRCh38#110478228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11481461-C-A

110478228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481461-C-G

110478228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481461-C-T

http://identifiers.org/hco/13/GRCh38#110478246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11481482-C-A

110478246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481482-C-G

http://identifiers.org/hco/13/GRCh38#110478249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11481485-A-C

110478265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481501-A-G

110478305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11481541-T-A

http://identifiers.org/hco/13/GRCh38#110479998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11483464-C-A

http://identifiers.org/hco/13/GRCh38#110480083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11483533-C-A

110480094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11483544-A-G

110480094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11483544-A-T

110480125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11483584-T-C

http://identifiers.org/hco/13/GRCh38#110480496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11483906-C-A

http://identifiers.org/hco/13/GRCh38#110482465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11484585-C-A

110482465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11484585-C-G

110482468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11484588-T-C

110482470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11484590-C-G

110482470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11484590-C-T

110482502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11484614-C-T

http://identifiers.org/hco/13/GRCh38#110482529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11484641-A-C

110482535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11484647-G-A

110482557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11484669-C-T

110482574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11484686-A-G

110482574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11484686-A-T

110482955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11485615-C-T

110484813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487499-G-A

110484813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487499-G-C

110484813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487499-G-T

http://identifiers.org/hco/13/GRCh38#110484814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487500-C-A

110484814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487500-C-G

110484814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487500-C-T

110484857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487540-G-A

http://identifiers.org/hco/13/GRCh38#110484884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487566-C-A

110485002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11487684-G-A

http://identifiers.org/hco/13/GRCh38#110485014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487696-C-A

110485014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 11487696-C-G

110485047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487742-G-A

http://identifiers.org/hco/13/GRCh38#110485063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487758-C-A

110485063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487758-C-T

http://identifiers.org/hco/13/GRCh38#110485078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487773-C-A

110485078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487773-C-T

http://identifiers.org/hco/13/GRCh38#110485089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487779-C-A

110485089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487779-C-G

110485089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487779-C-T

110485099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487787-T-A

110485099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11487787-T-C

http://identifiers.org/hco/13/GRCh38#110485671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11487940-A-C

110485725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11487994-C-G

110485779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 11488048-C-T

110485785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 11488054-G-C

110485809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 11488078-G-A

110489653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11488503-A-G

http://identifiers.org/hco/13/GRCh38#110489826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11488666-C-A

110489936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11488768-G-A

110489936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11488768-G-T

110489991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11488818-C-G

110492118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11489354-G-A

110492118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11489354-G-C

110492118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11489354-G-T

http://identifiers.org/hco/13/GRCh38#110492224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11489476-C-A

110492224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489476-C-T

110492303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489552-G-T

http://identifiers.org/hco/13/GRCh38#110492314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11489563-C-A

110492314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489563-C-G

110492314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489563-C-T

110492677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489870-G-A

110492677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11489870-G-C

http://identifiers.org/hco/13/GRCh38#110493190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11490358-C-A

110493190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11490358-C-T

110493194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11490362-G-A

110493340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11490498-T-A

110493340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11490498-T-C

110494957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11490844-C-G

110495194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11491073-G-A

110495257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11491123-G-A

110495407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11491287-G-A

110495487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11491355-G-A

110495497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11491361-C-T

110501660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11491872-A-G

110501660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11491872-A-T

110501821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11492002-T-A

110501821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11492002-T-G

110501931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11492074-T-C

110501931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11492074-T-G

110502002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11492150-G-A

110503195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11493145-G-A

110503195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11493145-G-C

110503318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493257-G-C

http://identifiers.org/hco/13/GRCh38#110503338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493271-C-A

110503338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493271-C-G

http://identifiers.org/hco/13/GRCh38#110503353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493286-C-A

110503353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493286-C-T

110503432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11493366-G-A

110503432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11493366-G-T

http://identifiers.org/hco/13/GRCh38#110503579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493450-C-A

110503579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493450-C-T

110503582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493453-G-T

110503637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11493502-C-T

http://identifiers.org/hco/13/GRCh38#110503971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493680-C-A

110503971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11493680-C-T

110504004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493713-G-C

110504004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493713-G-T

http://identifiers.org/hco/13/GRCh38#110504034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493739-C-A

http://identifiers.org/hco/13/GRCh38#110504067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493760-C-A

110504085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11493779-G-T

110504185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 11493868-A-G

http://identifiers.org/hco/13/GRCh38#110504318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11493994-C-A

110504318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11493994-C-T

110506515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 11495031-G-T

110506527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 11495043-A-G

110506527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 11495043-A-T

110506566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11495082-G-A

110506572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11495088-C-T

110506590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11495106-G-A

110506590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11495106-G-T

http://identifiers.org/hco/13/GRCh38#110506626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11495141-C-A

http://identifiers.org/hco/13/GRCh38#110506692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11495200-A-C

110506729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495220-T-C

110506729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495220-T-G

110507041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11495477-T-C

110507144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495571-C-G

110507144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495571-C-T

http://identifiers.org/hco/13/GRCh38#110507259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11495682-C-A

110507325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495746-A-G

http://identifiers.org/hco/13/GRCh38#110507369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11495789-C-A

110507369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495789-C-T

110507439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11495848-G-A

110507439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11495848-G-T

110507945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11495970-C-T

http://identifiers.org/hco/13/GRCh38#110508023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11496048-C-A

110508023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11496048-C-T

110508248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11496295-C-G

110508248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11496295-C-T

110508727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11495088-T-C

http://identifiers.org/hco/13/GRCh38#110512042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498167-A-C

110512056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 11498181-C-G

110512056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11498181-C-T

110512092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11498217-C-G

110512092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11498217-C-T

110512125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11498250-C-T

110512202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498335-G-T

http://identifiers.org/hco/13/GRCh38#110512319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498611-C-A

110512319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498611-C-T

http://identifiers.org/hco/13/GRCh38#110512369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498660-C-A

110512369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498660-C-G

110512369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498660-C-T

110512378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498675-T-A

110512378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498675-T-C

http://identifiers.org/hco/13/GRCh38#110512395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498692-C-A

http://identifiers.org/hco/13/GRCh38#110512529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498841-A-C

110512529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498841-A-G

110512529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498841-A-T

110512536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498846-T-C

110512536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498846-T-G

110512581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498887-G-A

110512581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498887-G-C

110512581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498887-G-T

http://identifiers.org/hco/13/GRCh38#110512609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498906-C-A

110512609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498906-C-G

110512609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498906-C-T

http://identifiers.org/hco/13/GRCh38#110512629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11498926-C-A

110512629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498926-C-T

110512633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498936-G-A

110512633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498936-G-C

110512633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11498936-G-T

110512829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11499104-G-T

http://identifiers.org/hco/13/GRCh38#110512861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11499133-C-A

110512861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11499133-C-T

110512971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11499242-A-G

110513004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11499281-A-G

110513009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2203
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11499286-G-T