79311305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89586909-G-A

79311382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89586832-G-A

http://identifiers.org/hco/15/GRCh38#79311468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89586776-C-A

79311468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89586776-C-G

79311468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89586776-C-T

http://identifiers.org/hco/15/GRCh38#79311533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89586712-C-A

79311533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89586712-C-T

79311620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89586626-C-T

79311718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89586531-C-T

79311967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89586287-G-A

79312346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585960-G-A

http://identifiers.org/hco/15/GRCh38#79313632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89585188-C-A

79313632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585188-C-T

79313664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585156-G-A

79313672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585148-T-G

79313679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585141-T-C

79313742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89585086-T-C

79313763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89585065-A-T

79313862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89584966-G-A

79313874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89584954-G-A

79313926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89584902-C-T

79314517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89584149-T-C

79314537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89584130-T-C

79314615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89584052-A-G

79314691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583980-G-T

79314692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583979-G-A

79314755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583913-G-T

79314760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583905-G-A

79314760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583905-G-C

79314760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583905-G-T

http://identifiers.org/hco/15/GRCh38#79314775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89583890-C-A

79314775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89583890-C-T

http://identifiers.org/hco/15/GRCh38#79314993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89583696-C-A

79315060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89583641-G-A

79316046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583266-T-C

http://identifiers.org/hco/15/GRCh38#79316063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89583251-C-A

79316063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583251-C-T

79316064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583250-G-A

79316064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583250-G-T

79316073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583241-C-G

79316079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583235-T-C

79316079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89583235-T-G

79317718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582687-A-G

79321425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582526-G-A

79321487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582466-G-A

79321592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582388-C-T

79321644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582332-C-T

79321656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582316-G-A

79321667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582305-C-T

79321809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582185-A-G

79321828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582161-T-G

79321853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582138-A-T

79321880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582121-G-A

79321880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582121-G-T

79321881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582120-G-C

79321881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582120-G-T

79321925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582085-T-G

79321952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89582056-G-A

79322128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89581880-C-T

79322200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89581808-G-A

79322200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89581808-G-T

79322218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581790-C-T

79322234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581775-G-A

http://identifiers.org/hco/15/GRCh38#79322352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581685-C-A

79322352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581685-C-T

http://identifiers.org/hco/15/GRCh38#79322363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581674-C-A

79322363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581674-C-T

79322449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581595-A-G

http://identifiers.org/hco/15/GRCh38#79322451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581593-A-C

http://identifiers.org/hco/15/GRCh38#79322491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581560-C-A

http://identifiers.org/hco/15/GRCh38#79322506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581545-C-A

http://identifiers.org/hco/15/GRCh38#79322642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581415-C-A

79322642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581415-C-G

79322741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581341-A-T

79322838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581255-G-A

79322838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89581255-G-T

79322876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581219-G-A

79322876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581219-G-T

http://identifiers.org/hco/15/GRCh38#79322878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581217-C-A

79322967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581134-G-T

http://identifiers.org/hco/15/GRCh38#79322989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581112-A-C

79322989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581112-A-T

http://identifiers.org/hco/15/GRCh38#79322997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581102-C-A

79322997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581102-C-T

http://identifiers.org/hco/15/GRCh38#79323000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89581099-C-A

79323009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581090-T-A

79323010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581089-G-A

79323020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581081-T-C

79323026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581075-G-T

79323034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581064-G-A

79323034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89581064-G-T

79323485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580666-C-G

79323603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580429-A-G

79323660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580356-A-G

79323661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580355-G-C

79323679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580337-T-C

79323679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580337-T-G

79323831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89580178-C-T

http://identifiers.org/hco/15/GRCh38#79323992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89580099-A-C

79324374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579945-G-A

79324422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579892-C-T

79324786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579568-G-A

79324823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579533-G-T

79325054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579308-G-T

79325216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579043-C-T

79325238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89579024-T-A

79325311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89578974-G-A

79325472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89578813-T-C

79325499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89578787-T-A

79325515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89578764-C-T

79327996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89577037-T-C

79328057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89576974-A-G

79328363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89576386-C-T

79337536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89571746-A-G

79337565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89571720-A-G

79337656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89571626-G-A

http://identifiers.org/hco/15/GRCh38#79338060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89571248-C-A

79338062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89571246-C-T

79338109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89571207-A-T

79338293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89570957-C-T

http://identifiers.org/hco/15/GRCh38#79339543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89570702-A-C

79339710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89570360-G-A

79339902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89570140-T-C

79339902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89570140-T-G

79340226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569821-C-T

79340247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569800-G-A

79340557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569493-G-A

79340750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569277-T-C

79340807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569219-C-T

79340826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569200-A-G

79340870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89569156-A-T

79341658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89568716-C-G

79341850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89568556-G-A

79341882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89568522-A-G

http://identifiers.org/hco/15/GRCh38#79352634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89566414-C-A

79354059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89565893-T-C

79354090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89565862-T-C

79354177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89565191-G-A

79354337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89565082-C-T

79354563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89564888-C-G

79354600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89564851-A-G

79354620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89564837-A-G

79355539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89563977-G-A

79355635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89563893-C-T

79355838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89563719-C-T

79368397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#79368412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

79370495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89559038-A-G

79370525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89559012-T-G

http://identifiers.org/hco/15/GRCh38#79370579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89558957-C-A

79370632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558898-C-G

79370632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558898-C-T

79370813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558744-T-C

79370930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558639-T-A

79371024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558545-C-G

79371052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558518-T-A

79371164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558411-C-T

79371169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558405-A-G

79371169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89558405-A-T

79372880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89557812-C-T

79372888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89557804-G-A

79372998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89557699-T-A

79380730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556860-A-G

79380825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556764-G-T

79380845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556745-A-G

79381059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556542-G-T

79381131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, undefined
orthologous variants: 89556541-T-C

79381425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556311-C-T

79381478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556284-G-A

79381534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556212-T-G

79381580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556167-T-C

79381720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89556051-G-A

79381777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89555990-G-A

79382134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89555491-G-A

79382143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89555482-A-G

79382173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89555459-G-A

http://identifiers.org/hco/15/GRCh38#79382279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89555355-A-C

79382365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89555267-C-T

79382691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89554960-A-G

79382763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89554903-A-G

79382794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89554871-A-G

79382912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89554751-T-C

79382940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89554722-C-G

79382968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 89554694-G-A

79382968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 89554694-G-T

http://identifiers.org/hco/15/GRCh38#79382972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89554690-C-A

79382972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron_variant, missense_variant
orthologous variants: 89554690-C-T

http://identifiers.org/hco/15/GRCh38#79383042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89554621-C-A

79383042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89554621-C-T

79383071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89554592-T-G

79393150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89553494-C-G

79393378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89553178-C-T

79393413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89553143-C-T

79393442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89553115-A-G

79393935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552551-G-A

79394242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552244-G-A

79394242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552244-G-C

http://identifiers.org/hco/15/GRCh38#79394304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89552185-A-C

79394304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552185-A-G

79394357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552131-A-G

79394387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552102-C-T

79394453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89552035-G-A

79394533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89551955-G-A

79398490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534425-G-A

79398525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534390-A-G

79398580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534357-G-A

79398603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534335-G-C

79398618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534313-C-T

79398646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534289-C-G

79398689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534254-G-A

79398689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534254-G-T

79398732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89534217-A-T

79399223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533942-C-G

79399223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533942-C-T

79399247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533918-C-T

http://identifiers.org/hco/15/GRCh38#79399259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89533906-C-A

79399259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533906-C-T

79399469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533719-A-G

79399502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533686-A-T

79399815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533370-G-T

79399868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533315-T-A

79399941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533242-T-C

79400030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533156-C-T

79400113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533053-C-T

79400122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533041-C-G

79400122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533041-C-T

http://identifiers.org/hco/15/GRCh38#79400131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89533032-A-C

79400131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89533032-A-G

79400179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532984-T-C

http://identifiers.org/hco/15/GRCh38#79400186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89532977-C-A

79400186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532977-C-T

79400215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532948-T-C

79400732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532492-G-C

79401078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532186-C-T

79401120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532141-T-C

79401172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532089-G-A

79401281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89532010-C-T

79401338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531954-A-G

79401421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531846-C-T

79401704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531595-T-C

79401803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531503-A-G

79401807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531499-G-T

79401829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531477-A-G

79401869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531436-C-T

79401965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531339-G-A

http://identifiers.org/hco/15/GRCh38#79401977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89531330-A-C

79401977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531330-A-T

79402016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531296-T-A

79402068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531260-A-G

79402198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89531113-G-C

79402262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89530978-C-G

79402262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89530978-C-T

79408575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89524763-G-T

79408636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89524707-A-G

79408787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89524563-G-T

79409172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89524242-C-T

79409696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89523732-T-C

79409945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89523469-G-A

79409963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89523451-G-T

79410182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89523217-A-G

79410262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89523136-T-G

79410410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522985-A-T

79410736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522682-A-G

79410947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522450-C-G

79411188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522222-G-A

79411252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522158-A-G

79411300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522115-A-G

79411317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: intron variant
orthologous variants: 89522098-A-G

http://identifiers.org/hco/15/GRCh38#79413291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521977-C-A

79413307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 89521961-G-A

http://identifiers.org/hco/15/GRCh38#79413310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521958-C-A

79413310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 89521958-C-G

79413310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 89521958-C-T

http://identifiers.org/hco/15/GRCh38#79413356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521913-C-A

79413419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 89521854-G-T

http://identifiers.org/hco/15/GRCh38#79413505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521775-C-A

79413505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 89521775-C-T

79413573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521709-C-T

79413576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521706-G-C

79413576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521706-G-T

79413603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521661-G-A

79413645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521620-C-T

79413677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521604-C-G

79413677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521604-C-T

79413685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521596-C-G

http://identifiers.org/hco/15/GRCh38#79413753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521533-C-A

79413753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521533-C-G

79413825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521469-T-G

79413863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521435-T-C

79415432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521333-A-G

79415702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521089-T-G

http://identifiers.org/hco/15/GRCh38#79415711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89521080-C-A

79415711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521080-C-G

79415744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89521048-T-C

79416143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89520544-A-G

79416156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89520531-T-C

79416445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89520260-G-A

http://identifiers.org/hco/15/GRCh38#79416906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89519856-C-A

http://identifiers.org/hco/15/GRCh38#79417035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89518540-C-A

79417037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518538-T-G

79417057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518516-A-G

79417070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518503-T-C

http://identifiers.org/hco/15/GRCh38#79417078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89518495-C-A

79417089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518480-G-T

79417095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518474-A-G

79417240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518342-A-G

79417420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518173-A-G

http://identifiers.org/hco/15/GRCh38#79417548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89518063-C-A

79417577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89518034-A-G

79417624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517990-G-A

79417742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517868-G-A

79417742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517868-G-T

79417835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517776-G-T

79417916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517696-G-T

79417921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517691-G-A

79417921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517691-G-T

79418023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89517595-G-A

79421718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514829-T-C

http://identifiers.org/hco/15/GRCh38#79421811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89514747-C-A

79421811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514747-C-G

79421960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514658-T-A

79421960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514658-T-C

http://identifiers.org/hco/15/GRCh38#79422012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89514610-C-A

79422012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514610-C-T

79422397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89514387-A-G

79423164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89513744-G-T

79423231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89513636-T-C

79423367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89513509-G-C

http://identifiers.org/hco/15/GRCh38#79423567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89513325-C-A

79423567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89513325-C-T

http://identifiers.org/hco/15/GRCh38#79423576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89513316-C-A

79423576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89513316-C-T

79423728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89512205-G-A

79423915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89512022-C-T

http://identifiers.org/hco/15/GRCh38#79424083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89511897-C-A

79424194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89511408-T-C

79424290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89511323-A-G

79424321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89511270-T-C

79424367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89511228-G-T

79424368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89511227-C-T

79424661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510957-G-C

79424889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510744-A-G

http://identifiers.org/hco/15/GRCh38#79424929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89510704-C-A

79424929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510704-C-T

79424939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510702-G-T

79425480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510460-T-C

79425566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510426-T-C

79425570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510422-A-G

79425610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510393-G-T

79425613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510389-A-T

79425633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510369-C-G

79425672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510330-C-G

79425700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510305-G-T

79425832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510174-T-C

79425891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89510119-A-G

79426028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509990-G-A

79426029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509989-G-A

http://identifiers.org/hco/15/GRCh38#79426042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89509976-C-A

79426138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509883-A-G

79426139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509882-G-A

79426139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509882-G-T

79426202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509820-G-A

79426202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509820-G-T

http://identifiers.org/hco/15/GRCh38#79426282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89509743-C-A

79426282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509743-C-G

http://identifiers.org/hco/15/GRCh38#79426366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89509678-A-C

79426743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509455-C-T

79426745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509453-G-A

79426745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509453-G-T

79426835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28889
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 89509360-T-A