184088812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47548473-T-C

http://identifiers.org/hco/4/GRCh38#184088955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47548367-C-A

184089015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47548307-C-T

184089030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47548291-A-G

184089192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47548131-G-A

184089332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547990-G-A

184089342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547981-G-T

http://identifiers.org/hco/4/GRCh38#184089436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47547794-C-A

184089436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547794-C-T

184090130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547227-A-G

184090182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547177-C-G

184090182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547177-C-T

http://identifiers.org/hco/4/GRCh38#184090190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47547169-A-C

184090190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547169-A-G

184090190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547169-A-T

184090347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547040-A-G

184090348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547039-G-C

184090348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547039-G-T

184090373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547024-G-A

184090373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47547024-G-T

184090611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546814-G-A

184090611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546814-G-C

184090611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546814-G-T

184090725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546675-A-G

184090753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546645-G-A

184090753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546645-G-T

184090793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546609-G-T

184090795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546607-G-T

184090816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546595-G-T

http://identifiers.org/hco/4/GRCh38#184090830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47546582-C-A

184090833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546579-G-T

184090854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546564-A-G

184090875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546543-G-A

184090875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546543-G-T

184090900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546518-G-T

184090906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546512-C-T

184090909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546509-G-A

184090909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546509-G-T

http://identifiers.org/hco/4/GRCh38#184091063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47546344-C-A

184091063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546344-C-T

184091126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546280-G-A

184091147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546257-G-A

184091147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47546257-G-T

184091223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47546186-G-C

184091313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 47546096-A-G

http://identifiers.org/hco/4/GRCh38#184091316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47546093-A-C

http://identifiers.org/hco/4/GRCh38#184091405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47546004-C-A

184091405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47546004-C-T

http://identifiers.org/hco/4/GRCh38#184091418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47545991-C-A

184091418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545991-C-G

184091418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545991-C-T

184091437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545967-G-A

184091437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545967-G-C

184091437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545967-G-T

184091541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47545880-G-A

184092134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47545590-G-A

184092201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47545540-C-G

184092236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47545503-G-A

http://identifiers.org/hco/4/GRCh38#184092251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47545489-A-C

184092251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47545489-A-G

184092443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47545296-A-T

184092789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544725-T-C

184092800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544714-G-T

184092959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544566-G-A

184093006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544518-G-A

184093040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544484-C-T

184093042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544481-T-C

184093062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47544461-T-C

184094453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543833-C-T

184094536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543765-T-C

184094702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543574-A-G

184094761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543514-C-T

184094775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543500-C-T

184094793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543481-A-G

http://identifiers.org/hco/4/GRCh38#184094934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47543350-C-A

184094934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543350-C-T

184095157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543132-A-G

184095203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47543087-T-C

184095979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47536833-A-G

http://identifiers.org/hco/4/GRCh38#184096133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47536674-A-C

http://identifiers.org/hco/4/GRCh38#184096386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47536455-A-C

184096482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47536340-T-C

184096776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47536054-G-A

184097122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535693-T-A

184097122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535693-T-C

184097130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535685-T-C

http://identifiers.org/hco/4/GRCh38#184097173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47535642-C-A

184097356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense_variant, undefined
orthologous variants: 47535460-G-T

184097402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535414-G-A

184097402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535414-G-C

184097402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535414-G-T

http://identifiers.org/hco/4/GRCh38#184097491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#47535340-C-A

184097491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535340-C-G

184097491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535340-C-T

184097502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535329-T-A

184097502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535329-T-C

http://identifiers.org/hco/4/GRCh38#184097504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47535327-C-A

184097504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47535327-C-T

184097523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47535308-C-G

184097952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534853-A-T

184098113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534710-C-T

184098175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534659-G-A

http://identifiers.org/hco/4/GRCh38#184098216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47534625-C-A

184098216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534625-C-T

184098250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534587-T-C

184098274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534567-T-A

184098793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534051-C-T

184098795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534049-C-T

184098879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534008-T-C

184098912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47534003-G-C

http://identifiers.org/hco/4/GRCh38#184099062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47533868-C-A

184099062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533868-C-T

184099080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533850-G-A

184099084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533846-C-G

184099105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533787-T-A

184099314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533608-C-T

184099437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533472-G-A

184099438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533471-G-A

184099507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47533404-C-T

184100134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47532810-C-T

184100305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47532640-C-T

184100331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47532618-C-T

http://identifiers.org/hco/4/GRCh38#184100351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#47532603-A-C

184100357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47532597-G-A

184100515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47532458-A-G

184101652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47532221-G-C

184101753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47532126-G-T

184101756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47532123-T-A

184101788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47532092-G-A

184101788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47532092-G-T

http://identifiers.org/hco/4/GRCh38#184101878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47531990-C-A

http://identifiers.org/hco/4/GRCh38#184101919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47531955-C-A

184101919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47531955-C-G

184101919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47531955-C-T

http://identifiers.org/hco/4/GRCh38#184102132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47531772-A-C

184102382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47531554-T-C

184102625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47531359-G-T

184102634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47531350-T-C

184102671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47531324-T-C

184102691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47531306-C-T

184102765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47531232-C-T

184103077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47530962-G-C

184103106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47530935-G-A

184103404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47530695-G-A

http://identifiers.org/hco/4/GRCh38#184103447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47530640-C-A

184103449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47530638-C-T

184103514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47530575-A-G

184103700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47529666-C-G

184103942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529430-G-A

184104034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529366-C-T

184104097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529290-G-T

184104134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529254-C-T

184104218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529164-C-T

184104224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529158-G-A

184104224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529158-G-T

184104381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529002-T-G

184104382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47529001-T-C

184104475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47528899-G-A

184104723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47528708-G-A

184110612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47524314-T-C

184110706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47524227-A-G

http://identifiers.org/hco/4/GRCh38#184110710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47524223-C-A

184110941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47523852-G-A

184111107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47523653-C-T

184111287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47523464-T-G

184111342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47523407-G-A

184112187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522525-T-C

184112308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522395-T-G

184112414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522292-G-A

184112452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522254-G-A

184112452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522254-G-T

http://identifiers.org/hco/4/GRCh38#184112453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47522253-C-A

184112453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522253-C-T

http://identifiers.org/hco/4/GRCh38#184112455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47522251-A-C

184112455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522251-A-T

184112483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522223-G-A

184112483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522223-G-T

http://identifiers.org/hco/4/GRCh38#184112487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47522219-C-A

184112576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47522136-T-C

184112706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47522024-G-A

184112706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47522024-G-C

184112706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47522024-G-T

184112968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521586-G-A

184113158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521394-G-T

184113259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521294-A-G

184113436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521169-C-T

184113449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521167-C-G

184113449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521167-C-T

184113518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521076-C-G

184113550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47521039-C-T

184114309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520780-C-T

http://identifiers.org/hco/4/GRCh38#184114431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47520612-A-C

http://identifiers.org/hco/4/GRCh38#184114475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47520567-A-C

184114495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520557-G-A

184114602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47520453-G-A

184114636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520419-G-A

184114672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520383-A-G

http://identifiers.org/hco/4/GRCh38#184114676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47520379-C-A

184114676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520379-C-T

184114677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520378-G-A

184114876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520202-G-C

184114943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520127-G-A

184114993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520086-A-G

184114993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47520086-A-T

http://identifiers.org/hco/4/GRCh38#184115128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47520019-C-A

184115296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519875-A-G

184115459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519723-A-G

184115577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519613-C-T

184115666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519526-C-T

184116826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519115-C-T

http://identifiers.org/hco/4/GRCh38#184116839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47519102-C-A

184116839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519102-C-G

184116839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47519102-C-T

184116944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47518998-T-C

184117490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47518788-T-C

184117503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47518780-G-T

184117539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47518753-G-A

184117680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47518622-T-A

184117725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47518582-G-A

184117829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense variant
orthologous variants: 47518476-G-A

184117829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: missense variant
orthologous variants: 47518476-G-C

184117924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47518379-A-G

184117926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47518377-A-G

http://identifiers.org/hco/4/GRCh38#184117961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47518342-C-A

184117961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47518342-C-T

184118024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47518282-A-T

184118363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47514757-T-C

184118426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47514700-G-T

184118498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47514603-G-A

184118779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47514341-G-A

184119018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47514047-A-G

184119229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513830-T-C

184119347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513587-G-A

184119375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513556-C-T

184119516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513318-A-G

184119535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513268-C-T

184119767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513044-G-A

184119767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47513044-G-C

http://identifiers.org/hco/4/GRCh38#184119909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47512879-C-A

184120064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512741-C-G

184120117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512629-C-G

184120117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512629-C-T

184120146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512602-A-G

184120195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512548-C-T

184120196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512547-C-T

184120199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512544-C-G

184120231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512515-G-T

184120270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512477-G-A

184120301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512439-T-C

184120420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512326-C-T

184120423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47512323-G-T

184120536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47511953-C-T

184120727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47511732-T-A

184121085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47510520-T-C

184121227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47510379-G-A

184121306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47510281-G-A

184121653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509950-G-A

184121653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509950-G-C

184121653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509950-G-T

184121658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509945-A-G

184121661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509942-A-G

http://identifiers.org/hco/4/GRCh38#184121667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47509936-C-A

184121772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509828-T-C

http://identifiers.org/hco/4/GRCh38#184121962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47509627-C-A

184122002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509587-C-T

184122144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509406-T-C

184122398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509134-A-G

184122487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47509049-A-G

184122693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47508820-C-T

http://identifiers.org/hco/4/GRCh38#184122704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47508808-A-C

184122884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47508623-A-G

184122945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47508568-C-T

184123305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47507929-C-T

184123323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47507911-G-A

184123323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47507911-G-C

184123530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47507708-C-T

184123663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47507585-C-G

http://identifiers.org/hco/4/GRCh38#184124451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47506449-C-A

184124752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47506199-T-A

184124834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47506128-G-A

http://identifiers.org/hco/4/GRCh38#184124929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47506040-C-A

184124929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47506040-C-T

184124939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47506028-C-G

184125174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47505776-T-A

184125412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47505559-C-T

184125484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47505473-G-A

184125517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47505437-G-A

184125572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47505383-C-G

184128791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47504761-T-C

184128834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47504717-A-G

184129206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47504349-T-C

184129297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47503943-C-T

184130089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47502399-G-C

184130152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47502338-T-C

184130618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47502178-G-T

184130909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501886-T-C

184131035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501762-C-T

184131112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501726-T-C

184131128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501710-C-T

184131150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501683-T-C

184131161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501672-C-G

184131164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47501669-T-C

184137800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47492321-A-G

184137942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47492171-G-A

184138067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47492088-C-G

184138067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47492088-C-T

184138199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491965-T-A

184138207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491957-A-T

184138287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491880-A-G

184138461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491750-T-G

http://identifiers.org/hco/4/GRCh38#184138463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47491748-C-A

184138542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491660-C-T

184138671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491514-T-G

184138752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491433-T-C

184138914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491294-A-G

http://identifiers.org/hco/4/GRCh38#184139084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47491133-C-A

184139099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491118-T-C

184139100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47491117-G-A

http://identifiers.org/hco/4/GRCh38#184141268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47490763-C-A

184141384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490646-G-A

184141700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490401-G-C

184141760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490343-T-C

184141803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490316-C-T

184141827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490302-A-G

184141912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490218-G-A

184142018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490122-G-T

184142037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490103-C-T

184142055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47490088-C-G

184142706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489484-G-A

184142929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489316-G-A

184142929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489316-G-T

184142978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489283-G-T

http://identifiers.org/hco/4/GRCh38#184142996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47489265-C-A

184142996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489265-C-T

184143033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489237-G-C

184143104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47489171-C-T

184143395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47488923-G-C

184143408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47488909-A-G

http://identifiers.org/hco/4/GRCh38#184149146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47488085-C-A

http://identifiers.org/hco/4/GRCh38#184149147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47488084-C-A

184149193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47488038-T-C

184149503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487975-G-A

184149518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487960-T-C

184150009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487551-G-A

184150187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487396-G-A

184150210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487373-G-A

184150210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487373-G-T

184150531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487053-G-A

184150572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47487012-T-C

184151639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47486308-T-A

184151771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47486184-T-G

184152138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47485638-C-T

184152218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47485512-G-A

184152452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47485232-A-T

184152538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47485159-T-G

184152604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47485100-G-T

184152858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -A-T

184152924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -A-T

http://identifiers.org/hco/4/GRCh38#184153014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -C-A

184153060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -C-G

184153060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -C-T

184153109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -T-A

http://identifiers.org/hco/4/GRCh38#184153823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47483373-C-A

184153823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47483373-C-T

184154077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47482795-C-G

184154129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47482743-G-A

184154155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47482721-T-C

184154218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47482669-T-C

184154335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47482554-A-G

184155134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481782-C-T

184155221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481695-T-A

184155234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481682-A-T

184155328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481607-A-G

184155356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481579-C-G

184155677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481161-T-G

184155689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47481151-G-A

184156219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47480499-G-A

184156337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47480300-G-A

184156385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47480230-T-C

184158029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479834-T-C

184158179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479696-A-G

184158202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479673-A-G

184158604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479269-T-A

184158637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479242-G-A

184158716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479164-G-A

184158733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479147-G-T

184158746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47479133-T-C

184162781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475495-A-T

184162853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475433-A-T

184162867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475392-G-A

184162868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475391-G-T

184162919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475333-C-G

184162919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475333-C-T

http://identifiers.org/hco/4/GRCh38#184162972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47475260-C-A

184162972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475260-C-T

184163023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475210-A-G

184163222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475044-A-T

184163252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47475015-C-G

184165454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47474586-C-T

184165531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474543-G-C

184165819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474294-A-G

184165821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474292-G-C

184165848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474265-G-A

http://identifiers.org/hco/4/GRCh38#184166048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47474067-A-C

184166078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474028-T-C

184166078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47474028-T-G

184166233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47473871-G-A

184166234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47473870-T-C

http://identifiers.org/hco/4/GRCh38#184166469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47473612-A-C

184166614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47473449-T-C

184167628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47470752-C-G

184167698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47470697-T-G

184167786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47470589-C-T

184167930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47470470-G-C

184168117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47470181-C-T

184168258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469886-G-A

184168271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469870-C-T

184168283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47469838-T-C

184168571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469531-G-T

184168610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, undefined
orthologous variants: 47469490-C-G

184168642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469458-C-G

184168642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469458-C-T

184168658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469429-G-A

184168706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469401-G-C

184168762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469347-A-T

184168917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469260-C-T

http://identifiers.org/hco/4/GRCh38#184168926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47469251-A-C

184168926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469251-A-T

184169064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47469107-A-G

http://identifiers.org/hco/4/GRCh38#184169184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47468972-C-A

184169332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47468814-G-A

184173250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466859-C-G

184173250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466859-C-T

184173293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466813-G-T

184173494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466647-G-A

184173526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466615-A-G

184173583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466557-A-T

184173664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466490-T-A

184173664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47466490-T-G

184174365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465891-C-T

184174382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465874-G-A

184174398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465857-G-T

184174503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465763-T-C

184174597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465672-G-T

http://identifiers.org/hco/4/GRCh38#184174602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -A-C

184174602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: -A-G

184174680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465598-T-A

184174680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465598-T-C

184174680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465598-T-G

http://identifiers.org/hco/4/GRCh38#184174690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47465484-A-C

184174690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465484-A-G

184174690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465484-A-T

184174699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465475-T-A

184174699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465475-T-C

184174699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465475-T-G

184174745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465390-C-T

184174881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47465206-A-G

184175665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47464843-T-C

http://identifiers.org/hco/4/GRCh38#184175678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47464830-C-A

184187691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47462967-T-C

184187798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47462870-T-C

184188041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47462618-C-T

184188115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47462556-C-T

184188158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47462513-C-G

http://identifiers.org/hco/4/GRCh38#184188744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47461968-C-A

184188744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461968-C-T

184189142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461443-T-C

184189176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461413-A-G

184189217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461398-G-A

http://identifiers.org/hco/4/GRCh38#184189219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47461396-C-A

184189220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461395-A-T

184189603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47461043-G-A

184189909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47460542-G-A

184190101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47460351-T-C

184190127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47460322-G-A

184190185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47460260-T-A

184190266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47460180-T-C

184190566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47459903-A-G

184190573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47459901-C-G

184190596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47459878-T-C

184190883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458903-G-T

184190920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458866-G-A

184190934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458852-T-C

184191174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458660-A-G

184191477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458341-C-T

184191495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458325-T-C

184191664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47458165-C-T

184191933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47457896-A-T

184191935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47457894-C-T

184191955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47457877-C-T

184197294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453835-T-C

184197410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453742-A-T

184197474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453682-T-C

184197475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453681-G-T

184197476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453680-C-T

184197913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453281-C-T

184197937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453257-G-T

184198058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453137-G-T

184198148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47453039-C-T

184198230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452945-G-A

184198269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452906-C-G

184198271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452904-A-G

http://identifiers.org/hco/4/GRCh38#184198298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47452877-C-A

184198314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452861-C-G

184198314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452861-C-T

184198364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452808-C-G

184198532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452638-A-T

184198540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452630-T-C

184198970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452313-G-A

184198983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452303-T-A

http://identifiers.org/hco/4/GRCh38#184199111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47452184-A-C

184199209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452089-G-C

184199267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47452029-T-G

184199402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47451802-A-G

184199460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47451744-T-G

184199800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47451434-A-T

http://identifiers.org/hco/4/GRCh38#184200601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47450813-C-A

184200601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450813-C-G

184200873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450565-C-T

184200920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450514-A-T

184201091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450331-A-G

http://identifiers.org/hco/4/GRCh38#184201111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47450311-C-A

184201111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450311-C-G

184201111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47450311-C-T

http://identifiers.org/hco/4/GRCh38#184201331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47450095-A-C

184201412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449962-G-A

184201496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449852-T-A

184201692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449660-T-C

184201798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449553-T-C

http://identifiers.org/hco/4/GRCh38#184201933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47449417-A-C

184201984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449373-T-A

184202001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449356-G-A

184202421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449168-G-A

184202433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449160-G-A

184202559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449030-C-T

184202576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47449013-A-T

184202613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47448976-T-C

http://identifiers.org/hco/4/GRCh38#184204113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47446343-C-A

184204137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47446319-A-G

184206577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47445418-A-G

184206662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47445321-A-G

184206715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47445268-T-C

http://identifiers.org/hco/4/GRCh38#184207059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47444975-C-A

184207199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444898-G-T

184207241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444855-C-T

184207243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444853-C-G

184207243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444853-C-T

184207487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444649-C-T

184207533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444603-G-A

184207572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444558-C-T

184207614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444518-G-A

184207694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444331-A-G

184207706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444319-G-A

184207749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444278-C-G

184207749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444278-C-T

184207882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444101-T-C

184207894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444089-G-A

184207903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444086-G-A

184207929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444060-T-C

184207942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47444046-C-T

184208225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47443612-A-G

184214274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47443605-C-T

184214276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47443603-G-T

184214380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47443505-G-A

184215171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442697-C-T

184215291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442581-T-A

184215309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442564-G-A

http://identifiers.org/hco/4/GRCh38#184215349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47442525-A-C

184215357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442517-T-A

184215508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442321-G-C

184215549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442290-A-G

184215630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442210-T-G

184215662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47442179-T-C

184215884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441921-T-C

184215923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441882-G-A

184216152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441648-C-T

184216153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441647-G-A

184216153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441647-G-C

184216164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441636-C-T

http://identifiers.org/hco/4/GRCh38#184216342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47441458-C-A

184216342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441458-C-T

184216422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441362-G-A

184216495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47441230-T-C

184216614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47441108-C-T

184216620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47441102-A-G

184216690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47441038-G-A

184216777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440990-A-G

184216804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440965-G-A

184216830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440939-T-C

http://identifiers.org/hco/4/GRCh38#184216890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440866-C-A

184216890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440866-C-G

184216890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440866-C-T

184216908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47440848-T-C

http://identifiers.org/hco/4/GRCh38#184216979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440793-C-A

http://identifiers.org/hco/4/GRCh38#184217093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440699-C-A

184217093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440699-C-G

184217093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440699-C-T

http://identifiers.org/hco/4/GRCh38#184217101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440691-C-A

184217101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440691-C-G

184217101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440691-C-T

184217312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440484-A-G

184217441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440356-T-A

184217441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440356-T-C

http://identifiers.org/hco/4/GRCh38#184217493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440309-A-C

184217493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440309-A-T

http://identifiers.org/hco/4/GRCh38#184217500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440306-A-C

184217500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440306-A-T

184217536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47440291-G-A

http://identifiers.org/hco/4/GRCh38#184217551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440276-C-A

http://identifiers.org/hco/4/GRCh38#184217566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440261-A-C

http://identifiers.org/hco/4/GRCh38#184217689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47440134-A-C

184217761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron_variant, missense_variant
orthologous variants: 47440062-G-A

184217841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47439983-C-G

http://identifiers.org/hco/4/GRCh38#184217872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47439952-C-A

184217872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 47439952-C-G

184217891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439935-A-G

184217992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439830-T-A

184217992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439830-T-C

184217992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439830-T-G

184218022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439776-A-G

http://identifiers.org/hco/4/GRCh38#184218110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47439686-C-A

http://identifiers.org/hco/4/GRCh38#184218111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#47439685-C-A

184218111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439685-C-T

184218375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47439438-T-C

184219437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23409
most severe consequence: intron variant
orthologous variants: 47438150-G-A