57694919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95781837-G-A

57694919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95781837-G-C

http://identifiers.org/hco/16/GRCh38#57694922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95781845-C-A

57694922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95781845-C-T

57695159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782009-A-G

57695379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782238-T-C

57695547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782399-C-T

57697851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782562-G-A

http://identifiers.org/hco/16/GRCh38#57697873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95782583-C-A

57697873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782583-C-T

http://identifiers.org/hco/16/GRCh38#57698009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95782696-C-A

57698009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95782696-C-G

57698009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95782696-C-T

57698054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95782744-T-G

57698140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95782830-C-T

57698165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782853-G-C

57698174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782862-C-G

57698174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95782862-C-T

57698714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783090-G-A

http://identifiers.org/hco/16/GRCh38#57698737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95783113-C-A

57698749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783124-G-A

57699004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 95783383-C-G

57699004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95783383-C-T

57699047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783426-A-T

57699160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783558-G-A

57699170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783568-A-G

57699486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95783964-A-G

57699690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784132-G-A

57699896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784802-C-T

http://identifiers.org/hco/16/GRCh38#57700005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95784889-C-A

57700005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784889-C-T

http://identifiers.org/hco/16/GRCh38#57700009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95784893-C-A

57700009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784893-C-T

57700017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784902-A-G

57700063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784931-T-G

57700216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 95785094-C-T

57700270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 95785148-G-A

57701365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95785283-G-A

57701365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95785283-G-T

57701462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95785354-G-A

57701520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95785413-A-G

57701529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95785422-T-C

57701581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95785470-A-G

57701863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785594-G-A

57701863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785594-G-C

57701863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785594-G-T

57701865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785596-G-A

57701871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785599-A-G

57701879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785607-G-C

57701879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785607-G-T

57701880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785608-G-A

57701880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785608-G-T

57701919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95785636-C-T

57702115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95785832-T-C

57702115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95785832-T-G

http://identifiers.org/hco/16/GRCh38#57702238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95786005-C-A

57702238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786005-C-T

57702289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786097-A-G

57702348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786153-C-T

57702437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786236-T-C

57702454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786253-G-A

57703440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786923-C-T

57703475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95786950-C-T

57704069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95787579-C-G

http://identifiers.org/hco/16/GRCh38#57704380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95787889-C-A

57704540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95788052-G-A

57704703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95788203-C-T

57704799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95788281-G-A

57704799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95788281-G-C

57704799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95788281-G-T

http://identifiers.org/hco/16/GRCh38#57704803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95788285-C-A

57704974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95788439-G-A

57705001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95788466-G-A

57705025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95788490-G-A

57705025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95788490-G-C

http://identifiers.org/hco/16/GRCh38#57707424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95788769-C-A

57707424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95788769-C-T

57707600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: missense variant
orthologous variants: 95788945-G-T

57707615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: missense variant
orthologous variants: 95788960-C-G

57707615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: synonymous variant
orthologous variants: 95788960-C-T

57707686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 95789031-G-A

57707791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, missense_variant
orthologous variants: 95789094-G-T

57707824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95789127-G-A

57707824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95789127-G-T

http://identifiers.org/hco/16/GRCh38#57707829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95789132-C-A

57707829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95789132-C-T

http://identifiers.org/hco/16/GRCh38#57707891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95789196-C-A

57718147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794505-C-T

57718148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794506-G-A

57718152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794510-C-T

57718211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794568-T-C

http://identifiers.org/hco/16/GRCh38#57718226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95794579-C-A

57718286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794620-G-A

http://identifiers.org/hco/16/GRCh38#57718492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95794820-C-A

57718492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794820-C-G

57718492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794820-C-T

57718541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794879-C-T

57718565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95794903-G-A

57718697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95795042-G-A

57718729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95795066-C-T

57720623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796378-C-T

57721420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796790-G-A

57721464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796840-G-A

57721562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796934-G-A

57721562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796934-G-T

57721572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796947-G-T

57721586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796960-G-A

57721595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95796971-G-C

http://identifiers.org/hco/16/GRCh38#57721648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95797012-C-A

57721648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797012-C-G

57721648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797012-C-T

57722293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797543-G-A

57722525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797706-G-C

57722562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797746-G-T

57722580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797761-C-G

57722580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797761-C-T

http://identifiers.org/hco/16/GRCh38#57722616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95797794-A-C

57722616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95797794-A-T

57722748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, missense_variant
orthologous variants: 95797904-A-G

57722801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 95797957-T-C

57722884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798037-G-A

57722893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798042-G-A

57722893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798042-G-C

57722894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798043-G-T

57722902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798051-T-C

http://identifiers.org/hco/16/GRCh38#57722914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95798066-C-A

57723048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: synonymous variant
orthologous variants: 95798217-C-T

http://identifiers.org/hco/16/GRCh38#57723144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95798313-C-A

57723163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798331-A-G

57723682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798727-T-A

57723682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798727-T-C

57723684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798729-T-A

57723684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95798729-T-C

http://identifiers.org/hco/16/GRCh38#57723811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95798799-C-A

http://identifiers.org/hco/16/GRCh38#57724493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95799237-C-A

57724493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799237-C-T

57724531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799268-G-A

57724531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799268-G-C

57724531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799268-G-T

57724582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799319-G-A

57724582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799319-G-T

57724673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: synonymous variant
orthologous variants: 95799428-G-A

57724766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: synonymous variant
orthologous variants: 95799521-T-C

http://identifiers.org/hco/16/GRCh38#57724847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95799602-C-A

57724847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799602-C-T

57724858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799613-G-A

57724858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799613-G-T

57724870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799625-T-C

57724919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799674-T-C

57724922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron variant
orthologous variants: 95799677-G-T

57725681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95800417-G-A

57725725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95800461-G-A

57725725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95800461-G-T

http://identifiers.org/hco/16/GRCh38#57725830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95800558-C-A

http://identifiers.org/hco/16/GRCh38#57725974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95800671-C-A

57726130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95800806-C-T

57726291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 95800966-T-C

http://identifiers.org/hco/16/GRCh38#57726433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95801117-C-A

57726569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95801362-G-A

57726569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95801362-G-T

http://identifiers.org/hco/16/GRCh38#57726628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95801442-A-C

57726721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95801514-C-T

57726724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95801517-G-T

http://identifiers.org/hco/16/GRCh38#57727014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95801746-C-A

57727346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95801879-A-G

57727379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95801912-T-G

57727471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95801998-G-A

57727519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802070-G-T

http://identifiers.org/hco/16/GRCh38#57727559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95802113-C-A

57727559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802113-C-T

57727715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802282-C-T

57727946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802517-T-A

57727959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802530-C-T

http://identifiers.org/hco/16/GRCh38#57728246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95802759-C-A

57728301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802795-G-A

57728301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95802795-G-T

57728500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95802988-G-A

57728500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95802988-G-T

57728641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803126-T-C

57728642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803127-G-A

57728642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803127-G-T

57728644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803129-G-A

57728644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803129-G-T

57728663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803148-C-T

57728673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803158-G-A

http://identifiers.org/hco/16/GRCh38#57728675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95803160-C-A

57728675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803160-C-T

http://identifiers.org/hco/16/GRCh38#57728693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95803178-C-A

57728693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803178-C-G

57728693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803178-C-T

57728728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803209-G-C

57728728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803209-G-T

57728753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803231-G-C

57730088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803278-G-A

57730088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803278-G-C

57730130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803307-T-G

57730213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803379-A-G

57730243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803409-G-A

57730285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803452-G-T

57730310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95803477-T-G

57730812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804199-G-A

57730812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804199-G-C

57730812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804199-G-T

57730876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804249-C-T

57730906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804283-T-A

57730915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804292-T-C

57730928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95804298-C-G

57730928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95804298-C-T

57730984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95804354-G-A

57731137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95804499-C-T

http://identifiers.org/hco/16/GRCh38#57731175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95804534-C-A

57731175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95804534-C-G

57731231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95804590-G-C

http://identifiers.org/hco/16/GRCh38#57731276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95804636-C-A

57731373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95804703-A-G

57731376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95804706-G-A

57731376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95804706-G-T

57731411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95804722-G-A

57731411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95804722-G-T

http://identifiers.org/hco/16/GRCh38#57731438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95804748-C-A

57731483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804797-G-T

57731573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804831-G-A

57731573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804831-G-T

57731616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804868-C-G

57731616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804868-C-T

http://identifiers.org/hco/16/GRCh38#57731662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95804914-C-A

57731662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804914-C-T

57731682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804934-G-A

57731682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804934-G-T

57731685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804937-G-A

57731697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95804949-G-T

http://identifiers.org/hco/16/GRCh38#57731760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95805022-C-A

57731760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: 95805022-C-T

http://identifiers.org/hco/16/GRCh38#57731776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95805039-C-A