http://identifiers.org/hco/6/GRCh38#96016063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25799737-C-A

96016063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25799737-C-T

http://identifiers.org/hco/6/GRCh38#96016068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25799732-C-A

96016068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25799732-C-T

96016175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25799624-T-C

96016191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25799610-T-C

96016191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25799610-T-G

96016210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 25799589-C-T

96016389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25799451-G-C

http://identifiers.org/hco/6/GRCh38#96016558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25799288-A-C

96016695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25799176-T-C

96017002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798903-C-T

96017038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798863-T-G

96017274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798630-T-C

96017342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798569-G-A

96017411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798512-T-C

96017758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798184-T-C

96017825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798117-G-A

96017848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798093-G-A

96017896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25798047-T-A

96018401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25797471-T-A

96018793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25797136-G-A

http://identifiers.org/hco/6/GRCh38#96018807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25797122-A-C

96019053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796980-A-G

96019099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796930-T-G

96019221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796829-A-G

96019276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796784-G-A

96019430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796700-T-C

96019512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796617-C-T

96019531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796594-G-C

96019629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796422-A-G

96019653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796394-G-A

http://identifiers.org/hco/6/GRCh38#96019707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25796311-C-A

http://identifiers.org/hco/6/GRCh38#96019834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25796211-C-A

96019936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796109-T-A

96019975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25796071-G-T

http://identifiers.org/hco/6/GRCh38#96020775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25795295-C-A

96020775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25795295-C-T

http://identifiers.org/hco/6/GRCh38#96020827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25795229-C-A

96020827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25795229-C-T

96020887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25795169-T-C

96020974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25795079-G-A

96020983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25795070-A-G

http://identifiers.org/hco/6/GRCh38#96021039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25795008-A-C

http://identifiers.org/hco/6/GRCh38#96021087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25794956-C-A

96021087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794956-C-T

96021185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794860-T-C

96021480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794596-C-T

96021633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794454-T-A

96021917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794206-T-G

96021922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25794201-T-G

96027030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25790453-C-T

http://identifiers.org/hco/6/GRCh38#96027284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25790275-A-C

96027311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25790238-A-G

96027413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25790147-T-C

96027488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25790083-C-T

http://identifiers.org/hco/6/GRCh38#96027539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25790049-A-C

96027682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25789879-C-T

96027747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25789820-T-A

96027958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25789614-C-T

96028076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25789520-A-G

http://identifiers.org/hco/6/GRCh38#96028267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25789340-A-C

96028345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25789266-C-G

96028909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25788838-A-G

96029399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25788360-G-C

96029628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25788168-G-T

96029741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25788063-T-A

96029749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25788055-T-A

96032098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25785214-A-G

96032158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25785181-T-A

96032474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784921-A-G

96032817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784593-A-T

96032910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784502-C-T

http://identifiers.org/hco/6/GRCh38#96033023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25784400-A-C

96033145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784276-A-G

96033280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784142-T-C

96033427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784066-G-A

96033478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25784027-C-T

96033531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783999-A-G

96033569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783951-A-G

96033714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783847-T-C

96033748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783821-A-T

96033879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783676-T-G

96033910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783639-A-G

96034060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783495-C-T

96034148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25783406-T-G

http://identifiers.org/hco/6/GRCh38#96034402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25782990-C-A

96034674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25782725-A-G

96034707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25782691-A-T

96036784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780952-T-C

http://identifiers.org/hco/6/GRCh38#96036799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25780938-C-A

96036799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780938-C-G

96036799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780938-C-T

96036805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780932-T-C

96036816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780922-T-C

96036865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780875-G-A

96036910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780830-T-C

http://identifiers.org/hco/6/GRCh38#96036920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25780821-C-A

96036929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780812-G-C

96036929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780812-G-T

96036932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780809-G-T

96037045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780699-A-G

96037130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780628-T-C

96037162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780600-A-G

96037162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25780600-A-T

96037829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25779187-A-G

96038096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25778945-G-A

http://identifiers.org/hco/6/GRCh38#96038898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25778307-C-A

96038898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25778307-C-G

96038907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25778300-C-G

96039285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777603-C-T

96039287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777601-A-G

96039362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777540-A-G

96039368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777534-G-A

96039368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777534-G-C

96039394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777506-T-G

96039457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777448-C-T

96039510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25777400-A-G

96039806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776975-A-G

96039889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776859-A-G

96039971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776731-T-C

96040002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776699-T-A

http://identifiers.org/hco/6/GRCh38#96040039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25776665-A-C

96040157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776567-A-G

96040157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776567-A-T

http://identifiers.org/hco/6/GRCh38#96040507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25776257-A-C

96040619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25776165-C-T

96040780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25775462-T-A

96040927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25775308-G-A

96041368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25774935-C-G

96048185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25774273-C-G

96048350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25774109-T-G

96048722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25773787-T-C

96048793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25773717-C-T

96048938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25773624-A-G

96049300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772702-A-G

96049551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772467-G-A

96049551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772467-G-C

96049644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772378-C-T

96049667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772356-G-A

96049679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25772330-T-A

96057822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25769361-A-T

96058087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25769107-A-G

96058227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768968-C-T

96058375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768816-G-A

http://identifiers.org/hco/6/GRCh38#96058448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25768746-C-A

96058614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768580-C-T

96058642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768552-T-G

96058685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768509-G-C

96058714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768480-G-A

96058722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768472-G-A

96058778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768414-A-T

96058786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768406-T-G

96059066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768145-T-A

96059131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25768079-T-A

96059230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767990-A-G

96059267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767960-A-G

96059270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767957-C-G

96059289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767938-G-A

96059748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767503-T-A

96059995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25767137-T-G

96060916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25766236-G-C

96061396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25765781-T-C

96063702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25764773-T-C

96063794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25764688-G-T

96064245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25764220-C-T

96065132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25763147-C-T

96065296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25762971-T-C

96065339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25762928-A-G

96065442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25762824-A-G

96065587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25762681-G-A

96065587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25762681-G-T

96066128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760766-G-C

96066146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760748-A-G

96066324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760517-T-C

96066447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760404-G-A

96066752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760085-G-A

96066756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760081-T-G

96066806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25760032-G-A

96067069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25759785-T-C

96067696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25759189-T-C

96067723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25759169-G-A

96067877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25759068-G-A

96067877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25759068-G-T

http://identifiers.org/hco/6/GRCh38#96067907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25759039-A-C

96069372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25750649-G-A

http://identifiers.org/hco/6/GRCh38#96069427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25750586-A-C

96069431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25750582-G-A

96069431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25750582-G-T

96069432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25750581-A-T

96069482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25750562-T-C

96073570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25747446-T-C

96073591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25747425-C-G

96073821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25747200-T-C

96073976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25747049-T-A

http://identifiers.org/hco/6/GRCh38#96074021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25747008-C-A

96074091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25746885-A-G

96074117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25746849-C-T

96074536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25746478-A-T

96076356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25741354-A-T

96076383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25741328-A-G

96076589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25741113-A-G

96076649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25741064-G-T

96076661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25741052-T-C

96076721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25740996-T-G

96084172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25739146-A-T

http://identifiers.org/hco/6/GRCh38#96084849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25737892-C-A

96084897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25737804-G-A

96084905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25737781-T-C

96085026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25737665-T-G

96085128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25737573-A-G

96085446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25737021-T-C

http://identifiers.org/hco/6/GRCh38#96085511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25736963-A-C

96085850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25736680-T-G

96086073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25736479-T-C

http://identifiers.org/hco/6/GRCh38#96086077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25736475-A-C

96098134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722867-T-A

96098410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722614-T-A

96098463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722529-C-G

96098541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722453-T-A

96098609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722401-T-C

96098734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722268-G-A

96098734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722268-G-C

96098767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25722234-C-T

96099069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721952-G-T

http://identifiers.org/hco/6/GRCh38#96099250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25721783-C-A

96099359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721688-C-T

96099702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721490-T-G

96099712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721481-G-T

96099722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721471-G-A

96099969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721233-C-T

96099994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721208-A-G

96100194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721009-G-A

96100194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25721009-G-C

96100427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25720877-G-A

http://identifiers.org/hco/6/GRCh38#96101979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25718821-C-A

http://identifiers.org/hco/6/GRCh38#96102067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25718738-A-C

96102115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25718696-T-C

96103222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25717326-T-C

96103228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25717320-C-T

http://identifiers.org/hco/6/GRCh38#96103519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25717062-C-A

96103519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25717062-C-T

96103585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25716997-A-G

96103743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25716848-T-A

96103912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25716596-T-C

96103978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25716526-C-G

96103988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25716516-A-T

96108609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25714196-G-A

96108614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25714191-T-C

96108688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25714117-T-C

96108818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25713994-C-T

96108996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25713844-T-C

96109093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25713746-T-C

96109104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25713735-G-C

http://identifiers.org/hco/6/GRCh38#96109448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25713399-A-C

96112462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25710246-A-G

http://identifiers.org/hco/6/GRCh38#96112845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25709754-C-A

http://identifiers.org/hco/6/GRCh38#96112860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25709741-A-C

96112962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25709571-A-G

96113030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25709503-C-T

96113187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25709337-A-G

96120629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25704087-A-T

96121239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703419-A-G

96121250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703408-T-C

96121349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703300-G-C

96121451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703200-G-T

96121453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703198-C-G

96121564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25703090-C-T

http://identifiers.org/hco/6/GRCh38#96123313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25698515-A-C

96123391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25698443-C-T

96123728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25698128-T-C

96124178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697763-G-A

96124178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697763-G-T

96124372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697654-G-A

96124372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697654-G-C

96124640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697431-T-A

96124654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697417-A-T

96124657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697414-C-G

96124780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697268-A-G

96124837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697211-T-A

96124859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697189-G-A

96124872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25697174-T-C

96125294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696807-A-G

96125320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696781-G-A

96125419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696695-G-A

96125511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696647-C-T

96125582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696580-G-A

96125676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696525-A-T

96125881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25696323-T-C

96130402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693746-C-T

96130420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693727-A-G

96130550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693609-A-G

http://identifiers.org/hco/6/GRCh38#96130622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25693543-C-A

96130725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693494-T-A

96130845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693418-T-G

96130853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693410-T-C

96130950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693362-A-G

96131140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693237-T-G

96131221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693175-A-G

96131288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25693114-A-G

http://identifiers.org/hco/6/GRCh38#96131377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25693038-A-C

http://identifiers.org/hco/6/GRCh38#96131663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25692777-C-A

96132295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691939-T-C

96132392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691705-C-T

96132429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691670-C-T

96132572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691551-A-G

96132721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691445-A-G

96132733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691433-G-T

96132738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691428-A-G

96132808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25691358-T-A

http://identifiers.org/hco/6/GRCh38#96133643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25690724-A-C

96133643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25690724-A-T

96133760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25690630-A-G

96133761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25690629-T-A

96133977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25689932-A-G

96134022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25689889-G-A

96134030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25689881-A-G

96134079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25689830-G-A

96134094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25689815-A-G

96138995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25687102-T-A

96138995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25687102-T-C

96141720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25681346-A-T

96141737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25681329-T-C

96141786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25681275-G-T

96142683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25680554-T-A

96142834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25680402-T-A

96143568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25677334-T-C

96143654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25677255-G-C

96143974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676984-A-G

96144061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676892-A-G

96144061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676892-A-T

96144063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676890-C-T

96144118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676762-G-A

96144140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25676740-G-C

96146625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25675660-G-T

96146897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25675397-T-C

96147120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25675174-C-T

96147919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25674391-G-A

96148316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25673984-T-A

96148320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25673980-T-G

http://identifiers.org/hco/6/GRCh38#96148392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25673792-A-C

96148392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25673792-A-G

96148392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25673792-A-T

96149218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25673287-G-A

http://identifiers.org/hco/6/GRCh38#96150132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25672848-A-C

96150281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25672740-G-A

96150582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25672476-T-C

96150688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25672379-G-A

96151116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25672040-A-T

96151228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25671925-T-C

96151604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25670322-G-A

96151724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25670212-G-A

96151787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25670149-C-T

96152078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669818-A-G

96152083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669813-G-A

96152172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669719-T-C

96152172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669719-T-G

96152350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669573-C-T

96152385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669543-C-G

96152385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669543-C-T

96152585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669369-A-G

96152741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669075-C-T

96152777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25669030-G-A

96152843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25668971-A-T

96152850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25668964-A-G

96152978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25668849-A-G

96153149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25668680-T-G

96153327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25668547-C-T

96155024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660358-T-C

96155077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660311-A-G

96155130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660228-A-G

96155152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660204-T-A

http://identifiers.org/hco/6/GRCh38#96155201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25660100-C-A

96155270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660030-G-A

96155286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25660014-T-C

96155349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25659946-T-G

96156794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25655265-C-G

96157310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25655770-C-T

96157723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656120-C-G

96157766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656163-A-G

96157773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656170-T-C

96157833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656229-T-A

96157978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656385-T-C

96158005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656412-A-T

96158011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656418-T-G

96158047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656454-A-G

96158050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25656457-G-T

96160325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657045-C-G

96160352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657067-C-G

http://identifiers.org/hco/6/GRCh38#96160396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25657098-A-C

96160396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657098-A-G

96160623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657312-A-G

96161042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657659-A-G

96161193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657787-G-T

96161201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25657795-G-T

96169689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644602-T-C

96169696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644595-G-A

96169774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644519-G-T

96170002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644294-A-T

96170018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644278-T-C

96170128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644175-A-G

96170227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644086-A-G

96170294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644002-C-G

96170294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25644002-C-T

96170472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643822-A-T

96170481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643814-T-C

96170587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643731-T-A

96170587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643731-T-C

96170663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643648-C-G

96170844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643482-A-G

http://identifiers.org/hco/6/GRCh38#96171058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25643295-C-A

96171094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643271-G-T

96171144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643221-A-G

96171151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643214-C-G

96171151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25643214-C-T

96172407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25642383-C-T

96172463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25642326-T-C

96172569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25642220-T-C

http://identifiers.org/hco/6/GRCh38#96172782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25640692-C-A

96172789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25640685-G-A

96172958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25640553-A-G

96173121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25640398-G-A

96173227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25640320-T-A

96173227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25640320-T-C

96173350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25639770-A-G

96173350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25639770-A-T

96173702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25639457-C-T

96174054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25639146-A-G

96174246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25638949-G-A

96174316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25638876-G-A

http://identifiers.org/hco/6/GRCh38#96174338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25638854-C-A

96174574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25637425-T-C

96174603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25637396-T-C

http://identifiers.org/hco/6/GRCh38#96174795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25637213-A-C

96174813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25637199-G-T

96174986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25637020-T-A

96175033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636978-T-A

http://identifiers.org/hco/6/GRCh38#96175110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25636918-C-A

96175110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636918-C-T

96175120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636908-G-T

96175176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636851-T-C

96175180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636847-G-A

96175294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636740-A-G

96175339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636694-T-G

96179825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636422-T-A

96179882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636365-G-T

96180170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25636092-T-G

96180281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25635984-A-T

96186175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25632262-T-C

96186262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25632175-A-G

96186550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25631894-A-G

96186978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25631516-C-T

96187155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25631394-C-T

96187336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25631256-C-T

96187338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25631251-A-G

96194450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25628069-G-T

96194697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25627847-T-C

http://identifiers.org/hco/6/GRCh38#96195132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25627363-A-C

96195132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25627363-A-G

96195219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25627274-T-C

http://identifiers.org/hco/6/GRCh38#96195806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25626689-A-C

96195860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626645-T-A

96195860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626645-T-G

96195924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626582-T-C

96195978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626506-T-C

96196084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626416-T-A

96196084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626416-T-C

96196084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25626416-T-G

96197420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, undefined
orthologous variants: 25627040-G-T

96197807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25625215-A-G

96197849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25625174-T-A

96197905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25625118-A-T

96197975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25625032-C-T

96198035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624972-G-A

96198035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624972-G-C

96199120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624744-T-C

96199190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624679-A-G

http://identifiers.org/hco/6/GRCh38#96199318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25624551-A-C

96199333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624536-T-A

96199333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624536-T-C

96199432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624444-A-G

96199582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624242-A-G

96199582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: 25624242-A-T

http://identifiers.org/hco/6/GRCh38#96199673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25624139-C-A

96199840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623950-T-C

96199898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623896-G-A

96200077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623744-T-C

96200097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623721-T-C

96200207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623608-C-G

96200383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25623443-C-T

96200487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25623343-G-A

96200570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25623301-G-T

96200824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25623176-G-A

96200879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25623145-T-A

96200980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25623047-T-C

96201083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622942-A-T

96201260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622755-C-T

96201339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622678-A-G

http://identifiers.org/hco/6/GRCh38#96201353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25622665-A-C

96201364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622654-T-G

96201453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622527-G-A

96201465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622513-A-G

96201568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622405-T-A

http://identifiers.org/hco/6/GRCh38#96201582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25622379-A-C

http://identifiers.org/hco/6/GRCh38#96201610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25622351-C-A

96201610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622351-C-T

96201618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622343-G-A

96201670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622104-T-C

96201673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25622101-T-G

96203029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25620924-T-C

96203029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25620924-T-G

96203093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25620869-G-A

http://identifiers.org/hco/6/GRCh38#96203122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25620844-C-A

96203122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25620844-C-T

96203196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 25620770-T-C

96203477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 25620489-A-T

96203882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 25620084-T-G

http://identifiers.org/hco/6/GRCh38#96204412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25619564-C-A

96204459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619518-G-T

96204469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619508-T-G

96204483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619494-T-A

96204483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619494-T-C

96204483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619494-T-G

96204516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619464-G-A

96204516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619464-G-C

96204516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619464-G-T

96204579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619404-G-C

96204579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619404-G-T

http://identifiers.org/hco/6/GRCh38#96204689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25619291-C-A

http://identifiers.org/hco/6/GRCh38#96204726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25619254-A-C

96204726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619254-A-G

96204726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619254-A-T

96204845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25619163-T-G

96205034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618957-A-G

96205170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618819-T-C

96205410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618600-A-T

96205481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618528-T-C

96205551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618460-A-G

96205579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618432-T-C

96205614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618395-G-A

http://identifiers.org/hco/6/GRCh38#96205630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25618379-C-A

96205637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618370-G-T

http://identifiers.org/hco/6/GRCh38#96205662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25618345-C-A

96205701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25618307-T-C

96206025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617969-T-C

96206052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617946-G-T

96206177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617902-T-C

96206410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617665-T-C

96206864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617579-G-T

96206892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617550-T-C

96206893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617549-T-A

http://identifiers.org/hco/6/GRCh38#96206934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25617508-C-A

96207091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617395-T-C

96207101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617385-A-G

96207104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617382-G-A

96207104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617382-G-T

96207220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617302-C-G

96207220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617302-C-T

http://identifiers.org/hco/6/GRCh38#96207255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25617267-C-A

96207255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617267-C-T

96207385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617143-T-G

96207402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617125-G-A

96207410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25617117-C-T

96207740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616807-G-A

96207982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616584-A-G

96207982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616584-A-T

96208021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616545-G-T

http://identifiers.org/hco/6/GRCh38#96208095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25616498-C-A

96208095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616498-C-T

http://identifiers.org/hco/6/GRCh38#96208100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25616493-C-A

96208100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616493-C-T

96208220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616364-T-A

96208220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616364-T-C

96208542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25616062-G-A

96208773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615844-G-C

96208773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615844-G-T

http://identifiers.org/hco/6/GRCh38#96208884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25615715-C-A

http://identifiers.org/hco/6/GRCh38#96208984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25615613-C-A

96208984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615613-C-T

96209015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615585-T-G

96209074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615538-T-C

96209221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615388-T-C

96209384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615256-G-A

96209384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615256-G-T

96209432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615215-G-C

96209432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615215-G-T

96209488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615163-G-T

96209553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615099-T-C

96209567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615085-A-T

http://identifiers.org/hco/6/GRCh38#96209594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25615061-C-A

96209594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615061-C-T

96209640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25615021-G-T

96210012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614617-T-C

96210051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614570-A-G

96210075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614551-G-A

96210077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614549-G-A

96210077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614549-G-T

96210276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614354-A-G

96210276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614354-A-T

96210374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614338-T-A

96210374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614338-T-C

96210463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614325-A-G

96210663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614221-A-T

96210853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25614054-C-T

96210923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613980-A-G

96210927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613976-T-C

96210965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613920-T-C

96211005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613867-G-A

96211018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613854-A-G

http://identifiers.org/hco/6/GRCh38#96211114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25613746-C-A

96211114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613746-C-T

http://identifiers.org/hco/6/GRCh38#96211163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25613693-C-A

96211163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613693-C-T

96211183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613673-A-G

96211190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613653-T-C

96211196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613646-G-A

96211196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613646-G-T

96211199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613643-G-A

96211200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613642-G-A

96211200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613642-G-T

96211217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613590-G-A

96211217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613590-G-T

96211234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613573-A-G

http://identifiers.org/hco/6/GRCh38#96211706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25613104-C-A

96211706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25613104-C-T

96211849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612973-G-A

96211989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612837-T-A

96212000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612823-T-C

96212020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612798-A-G

96212031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612787-A-G

96212037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612781-T-C

96212041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612776-T-C

http://identifiers.org/hco/6/GRCh38#96212045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25612772-C-A

96212065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612753-T-C

96212077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612741-G-A

96212077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612741-G-T

96212112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612707-C-T

96212113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612706-A-G

96212260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612562-C-T

96212264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612558-G-T

96212286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612530-G-C

96212416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612451-G-A

http://identifiers.org/hco/6/GRCh38#96212504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25612350-C-A

96212579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612284-G-T

96212601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612258-T-C

96212665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612215-A-T

http://identifiers.org/hco/6/GRCh38#96212825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25612100-C-A

96212825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25612100-C-T

96213056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611877-T-C

96213098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611850-C-G

96213177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611774-G-T

96213235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611730-A-G

96213423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611552-G-A

96213563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611421-G-A

96213563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611421-G-T

96213564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611420-T-C

96213613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611374-G-T

96213866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25611123-T-C

http://identifiers.org/hco/6/GRCh38#96213983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25611009-C-A

96214074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610912-G-A

96214074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610912-G-T

http://identifiers.org/hco/6/GRCh38#96214095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25610891-C-A

http://identifiers.org/hco/6/GRCh38#96214197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25610796-C-A

96214205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610788-T-C

96214205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610788-T-G

96214493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610511-G-T

96214589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610421-T-A

96214592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610418-G-C

96214991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25610016-G-T

96215003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25609975-C-T

http://identifiers.org/hco/6/GRCh38#96215031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#25609896-C-A

96215178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25609750-A-T

96215462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4020
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 25609478-T-C