114583055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103076859-T-C

114583222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103076696-C-T

114583315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103076614-T-C

114583346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103076583-A-G

114583440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103076490-A-G

http://identifiers.org/hco/1/GRCh38#114583896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103076444-C-A

114583945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103076398-T-A

114584017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103076310-A-G

114584709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075974-T-C

http://identifiers.org/hco/1/GRCh38#114584943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103075903-A-C

114585276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075599-A-G

114585281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075587-G-T

114585301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075567-A-G

114585351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075522-A-G

http://identifiers.org/hco/1/GRCh38#114585406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103075346-C-A

114585406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075346-C-T

114585552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075157-T-C

114585552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075157-T-G

114585625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103075091-T-C

114585653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103075063-G-A

114585654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103075062-T-G

114585664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103075053-A-G

114585664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103075053-A-T

114585727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074993-G-A

114585727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074993-G-T

http://identifiers.org/hco/1/GRCh38#114585750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103074970-C-A

114585750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074970-C-T

114586010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074239-T-C

114586046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074204-A-G

114586185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103074094-T-C

114586363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103073952-T-C

114586363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103073952-T-G

114587392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103073808-C-T

114587475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 103073725-T-G

114587695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103072578-G-T

114587711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103072563-C-T

114587930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103072344-C-T

114588061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103072176-G-A

114588061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103072176-G-T

114588548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103071763-T-A

114594305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070546-A-G

114594400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070467-T-C

114594400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070467-T-G

114594535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103070348-G-A

114594624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070273-A-T

114594679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070229-G-A

114594679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070229-G-T

114594700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070203-T-A

114594702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103070201-A-G

http://identifiers.org/hco/1/GRCh38#114594723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103069798-C-A

114594864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103069648-G-C

114595639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103069104-G-T

114595715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103069028-G-C

114595715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103069028-G-T

114595716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103069027-G-T

114595759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103068984-C-T

114595923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103068812-A-G

114599191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103065226-A-T

114599229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103065186-T-C

http://identifiers.org/hco/1/GRCh38#114599231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103065184-A-C

114599231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103065184-A-G

114599317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103065092-A-G

114599332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103065077-A-T

114599540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103064872-G-T

114600206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 103064262-T-C

114600237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103064231-T-A

114600237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103064231-T-C

114600270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103064198-T-A

114600349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103064119-T-C

114600349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103064119-T-G

114600591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103063703-A-G

114600654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103063644-A-G

http://identifiers.org/hco/1/GRCh38#114600763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103063550-C-A

114600763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103063550-C-G

114600763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103063550-C-T

114601272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103062831-C-T

http://identifiers.org/hco/1/GRCh38#114601390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103062024-C-A

114601390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103062024-C-T

http://identifiers.org/hco/1/GRCh38#114601447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103061970-C-A

114601447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061970-C-T

114601471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061916-A-G

114601496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061892-T-C

http://identifiers.org/hco/1/GRCh38#114601572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103061815-C-A

114601572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103061815-C-G

114601572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103061815-C-T

http://identifiers.org/hco/1/GRCh38#114601609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103061785-C-A

114601609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061785-C-G

114601609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061785-C-T

114601632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061761-T-C

114601654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061685-T-C

114601662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061668-A-G

114601674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061656-T-C

114601693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061643-A-G

114601693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061643-A-T

114601984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061379-G-A

114601984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061379-G-C

114601984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061379-G-T

http://identifiers.org/hco/1/GRCh38#114602026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103061115-C-A

114602026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061115-C-T

114602051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061090-G-T

114602072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103061069-T-C

http://identifiers.org/hco/1/GRCh38#114602144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103061001-C-A

http://identifiers.org/hco/1/GRCh38#114602256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103060909-A-C

114602930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103060663-C-T

114604564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103060000-T-C

114604678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059923-A-G

114604678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059923-A-T

114604694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059907-A-T

http://identifiers.org/hco/1/GRCh38#114604797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103059833-C-A

http://identifiers.org/hco/1/GRCh38#114604800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103059830-C-A

114604800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059830-C-T

114604809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059823-T-C

http://identifiers.org/hco/1/GRCh38#114604851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103059778-C-A

114604853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059776-A-G

114604872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059760-T-C

114604873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059759-T-G

114604979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103059659-A-G

114604991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103059647-C-G

114604991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103059647-C-T

114605900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059123-A-G

114605930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103059095-A-T

114606506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103057617-G-A

114606506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103057617-G-T

114608662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103056560-G-A

114608977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103056258-G-A

114608977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103056258-G-T

http://identifiers.org/hco/1/GRCh38#114609016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103056225-C-A

114609016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103056225-C-T

http://identifiers.org/hco/1/GRCh38#114609037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103056204-A-C

114609037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103056204-A-G

114609774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103054786-T-C

114609796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103054765-A-G

114610809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103054111-C-T

114610921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103054013-T-A

114611048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103053894-G-A

114611140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103053797-C-T

114611168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103053771-C-T

114611947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103052083-A-T

114614620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103049505-T-A

114618346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103048505-T-C

114618347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103048504-G-T

114618431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103048424-C-T

http://identifiers.org/hco/1/GRCh38#114618501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103048349-A-C

114618512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103048338-A-G

114618512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103048338-A-T

114618653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103047799-T-G

114618789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103047647-T-C

114619037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103047413-A-G

114619854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103046734-G-A

114620048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103046542-T-A

114620065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103046525-G-C

114620156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103046448-T-G

114620948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103045232-T-C

114621037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103045148-C-T

114621404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103044983-T-C

114621915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103044607-T-C

114621932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103044590-C-T

114622013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103044509-G-A

http://identifiers.org/hco/1/GRCh38#114622906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103041345-C-A

114622906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103041345-C-T

114622935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103041285-G-C

114622935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103041285-G-T

114622976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103041176-T-A

114623145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103041008-G-T

114623370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103040784-A-T

114623407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103040747-G-T

114623590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103040576-G-A

http://identifiers.org/hco/1/GRCh38#114625142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103039687-A-C

114625167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103039661-A-G

http://identifiers.org/hco/1/GRCh38#114625184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103039640-A-C

114625187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103039637-T-A

114625187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103039637-T-G

114625199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103039625-T-A

114625341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense variant
orthologous variants: 103039483-C-T

114625380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense variant
orthologous variants: 103039444-T-A

114625531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense variant
orthologous variants: 103039293-T-C

http://identifiers.org/hco/1/GRCh38#114625606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103039218-A-C

114625606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense variant
orthologous variants: 103039218-A-G

114625714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103039110-C-G

114625714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103039110-C-T

114625995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103038859-G-T

114626008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103038846-G-A

114626008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103038846-G-T

http://identifiers.org/hco/1/GRCh38#114626080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103038776-A-C

114626095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103038761-T-C

114626148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 103038707-G-T

http://identifiers.org/hco/1/GRCh38#114626196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103038659-A-C

114626289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103038573-T-C

114626542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103038379-G-A

114626542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103038379-G-C

114626542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103038379-G-T

114626954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103038036-T-C

114627846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103036765-C-T

http://identifiers.org/hco/1/GRCh38#114627947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103036694-A-C

114627979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103036660-G-T

114628859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103036009-A-G

114629123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103035784-T-C

114629680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103035574-T-A

114629867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103035434-G-A

114629867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103035434-G-C

114630317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103035009-A-G

114642514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103026478-T-C

114642521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103026471-G-C

114642521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103026471-G-T

114642819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103026152-T-C

114643128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025709-T-C

114643250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025597-A-G

114643273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025581-G-A

114643391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025316-A-G

114643529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025163-T-C

114643616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025087-A-T

114643623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103025080-G-A

114650791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103019934-T-C

114657783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103017982-C-G

114657783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103017982-C-T

114657794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103017971-G-A

114657942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103017830-C-T

114665716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103015280-T-C

http://identifiers.org/hco/1/GRCh38#114666101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103015015-C-A

114666130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103014991-A-T

114667224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103014213-C-T

114667716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013660-G-A

114667758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013623-G-A

114667876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013507-T-C

114667899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013478-T-C

114668033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013355-T-C

114668047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103013342-T-C

114668390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103012094-A-G

114668505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103011334-C-T

http://identifiers.org/hco/1/GRCh38#114669325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103010539-C-A

114669325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103010539-C-T

114669326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103010538-C-T

http://identifiers.org/hco/1/GRCh38#114669736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103010212-A-C

114669922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103010106-G-A

114669922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103010106-G-T

114669951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103010080-A-G

114669951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103010080-A-T

http://identifiers.org/hco/1/GRCh38#114669955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103010077-C-A

114669955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103010077-C-T

http://identifiers.org/hco/1/GRCh38#114669957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103010075-C-A

http://identifiers.org/hco/1/GRCh38#114670027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103010005-C-A

114670027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103010005-C-T

114670030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103010002-G-A

114670030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103010002-G-T

114670058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103009964-C-G

114670058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103009964-C-T

http://identifiers.org/hco/1/GRCh38#114670106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103009910-A-C

114670106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103009910-A-T

http://identifiers.org/hco/1/GRCh38#114670111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103009905-C-A

114670150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103009859-T-C

114670191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103009821-C-T

114670356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24748
most severe consequence: non coding transcript exon variant
orthologous variants: 103009712-A-G