109278289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 114392485-G-A

109278289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 114392485-G-T

109278334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392528-G-T

109278409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392540-G-T

http://identifiers.org/hco/12/GRCh38#109278419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114392550-C-A

109278479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392601-A-G

109278678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392779-G-A

109278692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392782-G-T

109278719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392809-G-A

109278762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114392852-G-T

109278938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393038-G-A

http://identifiers.org/hco/12/GRCh38#109278949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393049-C-A

109278949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393049-C-G

109278949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393049-C-T

http://identifiers.org/hco/12/GRCh38#109279072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393123-A-C

109279072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393123-A-G

109279117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393149-T-G

http://identifiers.org/hco/12/GRCh38#109279120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393152-A-C

109279120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393152-A-G

http://identifiers.org/hco/12/GRCh38#109279233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393239-C-A

109279233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: 114393239-C-G

http://identifiers.org/hco/12/GRCh38#109279298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393305-A-C

http://identifiers.org/hco/12/GRCh38#109279404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393392-C-A

109279404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 114393392-C-G

109279404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 114393392-C-T

109279424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 114393401-G-T

109279454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114393425-A-G

109279664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 114393545-T-C

http://identifiers.org/hco/12/GRCh38#109279734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393612-C-A

109279734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 114393612-C-G

109279734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 114393612-C-T

109279755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 114393636-A-G

109279863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114393744-G-A

109279863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114393744-G-T

109279884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114393765-T-C

109280055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114393827-G-A

109280055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114393827-G-T

109280067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114393839-G-A

109280067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114393839-G-T

http://identifiers.org/hco/12/GRCh38#109280407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114393958-C-A

109280524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394053-G-A

109280525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394054-A-G

109280740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394198-G-A

109281068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394465-G-A

109281308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394543-G-A

109281308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394543-G-C

109281308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394543-G-T

http://identifiers.org/hco/12/GRCh38#109281316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114394551-C-A

109281316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394551-C-T

109281317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394552-A-G

109281360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114394571-T-C

109281444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394657-A-G

109281535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114394748-T-C

http://identifiers.org/hco/12/GRCh38#109281603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114394816-C-A

109281603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394816-C-T

109281663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394876-G-C

109281663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394876-G-T

109281711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394924-G-A

109281711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114394924-G-T

109281750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394963-G-A

109281750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114394963-G-T

109281804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114395017-A-G

109281827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114395040-G-C

109281827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114395040-G-T

http://identifiers.org/hco/12/GRCh38#109281839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114395050-C-A

109281895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114395089-G-A

109281895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114395089-G-T

109281929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114395115-T-C

109281941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114395127-T-A

109284568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396527-C-T

109284572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396531-C-T

109284573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-G-A

109284573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-G-T

109284591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396550-T-C

109284600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-C-T

109284678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396550-G-A

109284691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-C-T

109284779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-T-A

109284779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-T-G

109284810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-T-C

109284860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396609-C-G

109284860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396609-C-T

109284941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-T-C

109285067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-C-G

109285237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396609-C-T

109285262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396527-T-C

109285262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396527-T-G

109285266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396531-T-C

109285266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396531-T-G

109285267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-G-A

109285267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396532-G-T

http://identifiers.org/hco/12/GRCh38#109285285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114396550-C-A

109285285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396550-C-T

http://identifiers.org/hco/12/GRCh38#109285294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114396559-C-A

109285294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-C-G

109285294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396559-C-T

http://identifiers.org/hco/12/GRCh38#109285344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#114396609-C-A

109285344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 114396609-C-T

109285383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 114396648-G-A

109285428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 114396693-G-A

109285428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 114396693-G-T

109285452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 114396717-G-A

109285452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 114396717-G-C

109285500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114396765-G-A

109285569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396865-G-A

109285569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396865-G-C

109285597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396893-G-T

109285616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396901-G-A

109285616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396901-G-T

109285659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114396930-A-G

http://identifiers.org/hco/12/GRCh38#109285902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397244-A-C

109285925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397267-G-A

109286229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397535-T-G

http://identifiers.org/hco/12/GRCh38#109286316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397592-A-C

109286549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397727-G-A

109286549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397727-G-T

109286550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397728-G-C

109286550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397728-G-T

http://identifiers.org/hco/12/GRCh38#109286608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397770-C-A

109286609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397771-A-G

http://identifiers.org/hco/12/GRCh38#109286613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397775-C-A

109286613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114397775-C-T

109286681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 114397844-G-A

109286681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: 114397844-G-T

http://identifiers.org/hco/12/GRCh38#109286711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397874-C-A

109286735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114397898-G-A

109286735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114397898-G-T

109286758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114397920-G-A

109286758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114397920-G-T

109286813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114397949-G-T

http://identifiers.org/hco/12/GRCh38#109286815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114397951-C-A

109286815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114397951-C-T

109286863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 114398000-T-A

http://identifiers.org/hco/12/GRCh38#109286947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114398088-C-A

109286947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398088-C-T

109287151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398254-G-A

109287335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398374-C-G

109287335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398374-C-T

109287336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398375-A-G

109287385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398399-C-T

109287389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114398403-G-A

109287452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114398466-G-A

109287491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114398505-C-T

109287551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398553-A-G

109287637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398625-G-A

109287637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114398625-G-T

109287923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114399006-G-A

109287974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399067-G-T

109287995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399091-G-A

109287995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399091-G-C

109288041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399121-T-A

109288041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399121-T-C

109288056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 114399136-G-A

109288056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 114399136-G-T

109288145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114399228-C-T

http://identifiers.org/hco/12/GRCh38#109288152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114399235-A-C

109288152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114399235-A-G

109288166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114399249-C-T

109288207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399290-G-A

109288207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399290-G-T

http://identifiers.org/hco/12/GRCh38#109288232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114399313-C-A

109288232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399313-C-T

109288310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399387-G-T

109288515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114399555-A-G

109288779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114399809-A-G

http://identifiers.org/hco/12/GRCh38#109288834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114399854-C-A

109288834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114399854-C-G

109289265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114400075-A-G

109289531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114400574-G-T

109289777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114400799-C-T

109289871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 114400883-C-G

http://identifiers.org/hco/12/GRCh38#109290002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114400982-C-A

109290012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114400992-G-T

http://identifiers.org/hco/12/GRCh38#109290114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114401057-C-A

109290114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114401057-C-T

109290133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114401062-G-A

109290133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114401062-G-C

109290208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114401137-A-T

109290224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 114401153-G-A

109290232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114401161-C-T

109290261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, missense_variant
orthologous variants: 114401190-C-T

109291001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114401513-T-G

http://identifiers.org/hco/12/GRCh38#109291020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114401532-C-A

http://identifiers.org/hco/12/GRCh38#109291083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114401601-C-A

http://identifiers.org/hco/12/GRCh38#109291093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114401611-C-A

109291100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114401618-G-T

109291263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114401792-C-T

109291302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114401827-G-A

109291302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114401827-G-T

109291566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114402035-C-T

109291786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114402250-G-A

109291817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114402282-G-A

109291824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114402289-G-A

109291831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114402296-G-A

http://identifiers.org/hco/12/GRCh38#109295818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114403735-C-A

109295818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114403735-C-T

109295888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114403788-G-A

109295888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114403788-G-T

109296146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114403980-G-A

109296147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114403981-C-G

109296406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114404227-C-T

109296505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114404318-G-A

109296505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114404318-G-T

109299138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114404921-C-T

109301979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114406272-A-G

http://identifiers.org/hco/12/GRCh38#109302149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114406407-C-A

http://identifiers.org/hco/12/GRCh38#109302161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114406410-A-C

109302245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114406483-C-T

109302457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114406635-T-C

109302741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114406901-T-C

109302807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, undefined
orthologous variants: 114406924-A-T

109303140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407260-T-A

109303201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407296-C-G

109303262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407359-G-A

109303262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407359-G-C

109303751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407805-G-A

109303828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407886-T-A

109303828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114407886-T-C

109304619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408223-G-A

109304624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408228-A-T

109304683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408289-G-A

109304683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408289-G-T

109304759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408395-G-A

109304844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114408478-G-A

109306078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114409195-G-T

109306426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114409437-G-A

109306495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114409547-G-T

109306669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114409704-G-A

109307087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114410035-T-G

109307713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114410609-C-T

109308223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114411021-T-C

109308330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 114411133-G-A

http://identifiers.org/hco/12/GRCh38#109308388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114411190-C-A

109308418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114411226-G-A

109308418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114411226-G-T

http://identifiers.org/hco/12/GRCh38#109308421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114411229-C-A

109308782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114411522-G-A

http://identifiers.org/hco/12/GRCh38#109309079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114411713-C-A

109309079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21399
most severe consequence: intron variant
orthologous variants: 114411713-C-T