http://identifiers.org/hco/14/GRCh38#24052105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728637-C-A

24052105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55728637-C-T

24052107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55728639-G-T

http://identifiers.org/hco/14/GRCh38#24052240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728785-C-A

24052240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55728785-C-G

http://identifiers.org/hco/14/GRCh38#24052284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55728825-C-A

24053290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, undefined
orthologous variants: 55729872-C-T

24053590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730228-G-A

24053590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730228-G-C

24053590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730228-G-T

http://identifiers.org/hco/14/GRCh38#24053614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55730250-A-C

24053614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, undefined
orthologous variants: 55730250-A-G

24053614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, undefined
orthologous variants: 55730250-A-T

http://identifiers.org/hco/14/GRCh38#24053653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55730274-A-C

24053705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55730325-T-A

24053752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: synonymous variant
orthologous variants: 55730372-A-G

24053791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 55730411-G-A

24053820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730440-T-G

24053824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730444-G-T

24053878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730468-G-A

24053937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730524-G-A

24053937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730524-G-T

24054170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730763-G-A

24054361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730946-G-A

24054363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55730948-G-A

24054443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 55731028-A-G

http://identifiers.org/hco/14/GRCh38#24054680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55731254-C-A

24054680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55731254-C-T

24054750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: synonymous variant
orthologous variants: 55731324-G-A

http://identifiers.org/hco/14/GRCh38#24054921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55731489-C-A

24054921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55731489-C-T

24054938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55731506-T-G

http://identifiers.org/hco/14/GRCh38#24055041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55731611-A-C

24055190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55731759-T-C

http://identifiers.org/hco/14/GRCh38#24055191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55731760-A-C

24055368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55731928-C-T

24055473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732043-T-C

24055521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732090-G-T

24056059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732576-G-C

24056212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732768-A-G

24056216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732772-A-G

24056216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55732772-A-T

http://identifiers.org/hco/14/GRCh38#24056600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55733162-C-A

24056600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733162-C-G

24056600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733162-C-T

24056729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733287-T-C

24056729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733287-T-G

24057071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733595-G-A

24057071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733595-G-C

24057071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733595-G-T

24057125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron variant
orthologous variants: 55733644-C-T

http://identifiers.org/hco/14/GRCh38#24057345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55733866-C-A

http://identifiers.org/hco/14/GRCh38#24057360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55733881-C-A

24057360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55733881-C-G

24057360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55733881-C-T

24057532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734036-C-T

http://identifiers.org/hco/14/GRCh38#24057695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55734182-C-A

24057695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734182-C-T

24057800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55734241-C-T

24057935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734375-G-A

24057943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55734383-C-T

24058023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55734461-C-G

24058023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55734461-C-T

24058234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734674-C-T

24058316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734742-G-A

24058316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734742-G-T

http://identifiers.org/hco/14/GRCh38#24058317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55734743-C-A

24058317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55734743-C-T

http://identifiers.org/hco/14/GRCh38#24058488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#55734960-A-C

24058574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55735030-T-A

24058574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55735030-T-G

24059028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735438-T-C

http://identifiers.org/hco/14/GRCh38#24059058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55735468-C-A

http://identifiers.org/hco/14/GRCh38#24059122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55735532-C-A

24059122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735532-C-T

24059200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735610-G-A

24059201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735611-G-C

24059395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55735801-C-T

24059552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735934-A-G

http://identifiers.org/hco/14/GRCh38#24059574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55735956-C-A

24059574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735956-C-T

24059582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55735964-T-C

24059640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

24059640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

24059918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736253-G-T

24059976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55736311-C-T

24060076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736414-G-A

24060076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736414-G-T

24060101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736439-G-A

24060101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736439-G-C

24060106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736444-G-A

24060106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736444-G-T

24060123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736466-C-T

http://identifiers.org/hco/14/GRCh38#24060299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55736633-A-C

24060299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736633-A-G

http://identifiers.org/hco/14/GRCh38#24060372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55736683-C-A

24060372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736683-C-T

24060428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736728-T-C

24060428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736728-T-G

http://identifiers.org/hco/14/GRCh38#24060530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55736838-C-A

24060530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736838-C-T

24060597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55736884-T-G

http://identifiers.org/hco/14/GRCh38#24060881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737165-C-A

24060881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737165-C-T

http://identifiers.org/hco/14/GRCh38#24061163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737428-C-A

24061163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737428-C-G

24061163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737428-C-T

http://identifiers.org/hco/14/GRCh38#24061175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737440-C-A

24061175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737440-C-G

24061175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737440-C-T

http://identifiers.org/hco/14/GRCh38#24061203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737460-C-A

24061203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737460-C-G

24061203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737460-C-T

24061219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737479-T-C

http://identifiers.org/hco/14/GRCh38#24061220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737480-C-A

24061220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737480-C-T

24061327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/14/GRCh38#24061357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737617-C-A

24061357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737617-C-T

24061395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737655-G-T

http://identifiers.org/hco/14/GRCh38#24061427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737689-C-A

24061427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737689-C-T

24061508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55737761-G-A

24061529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55737782-G-A

24061529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55737782-G-C

24061589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55737842-G-A

24061634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55737887-G-A

24061707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737957-G-T

24061713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737963-G-T

http://identifiers.org/hco/14/GRCh38#24061722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55737972-A-C

24061722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737972-A-T

24061729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737979-G-A

24061729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55737979-G-T

24061806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738049-T-C

24061868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738111-G-A

24061870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738113-T-A

24061870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738113-T-G

24061940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738189-G-T

24061961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738215-G-A

24061961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738215-G-T

http://identifiers.org/hco/14/GRCh38#24062010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55738264-C-A

24062010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738264-C-T

24062019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738273-A-G

24062019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738273-A-T

24062054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738306-G-A

24062228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738429-G-T

24062276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738480-G-A

24062276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738480-G-C

24062276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738480-G-T

24062293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738516-G-A

24062293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738516-G-T

24062342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738566-A-G

24062342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738566-A-T

24062380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738597-A-T

http://identifiers.org/hco/14/GRCh38#24062391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55738607-C-A

24062391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738607-C-G

24062391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738607-C-T

24062398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738614-G-T

24062416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55738635-G-A

24062537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55738746-G-C

24062619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55738824-A-G

24062619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55738824-A-T

24062741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55738948-A-G

24062909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55739111-A-G

http://identifiers.org/hco/14/GRCh38#24063013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55739212-C-A

http://identifiers.org/hco/14/GRCh38#24063110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55739277-A-C

24063110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55739277-A-G

24063110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55739277-A-T

24063380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55739737-C-T

24063540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55739897-C-T

24063577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55739933-A-G

24063869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740064-G-A

24063871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740066-A-G

24063872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740067-G-A

24064175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740324-T-C

24064175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740324-T-G

24064181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740340-G-C

24064181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740340-G-T

24064272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55740414-G-C

24064357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740542-T-C

24064373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740558-T-C

http://identifiers.org/hco/14/GRCh38#24064431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55740607-C-A

24064431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740607-C-T

24064444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740620-G-A

http://identifiers.org/hco/14/GRCh38#24064477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55740875-C-A

24064477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55740875-C-T

24064700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55741080-G-A

http://identifiers.org/hco/14/GRCh38#24064761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55741134-A-C

24064869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55741212-G-A

24064869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55741212-G-T

24064938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55741273-C-T

24064984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741320-G-A

24064984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741320-G-T

24065006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55741342-G-A

http://identifiers.org/hco/14/GRCh38#24065040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55741376-C-A

http://identifiers.org/hco/14/GRCh38#24065126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55741462-A-C

24065126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55741462-A-G

24065126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55741462-A-T

24065130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741466-C-T

24065218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741554-G-A

24065218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741554-G-T

24065221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55741557-G-T

http://identifiers.org/hco/14/GRCh38#24065371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55741709-C-A

24065371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741709-C-G

24065371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741709-C-T

24065394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741732-T-C

24065394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741732-T-G

24065462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741776-T-C

24065525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55741840-G-A

24066143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742615-T-C

24066165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742635-T-A

24066165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742635-T-C

24066253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742708-G-T

24066344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742801-T-A

24066344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55742801-T-C

24066646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55743106-A-G

24066684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743145-G-A

24066795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55743245-G-T

24066898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55743338-T-C

24067235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55743663-A-G

http://identifiers.org/hco/14/GRCh38#24067853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55744194-C-A

24067853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55744194-C-T

24068165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55744476-G-A

24068165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55744476-G-C

24068605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55744596-A-G

24068655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55744646-G-A

24068660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55744651-G-A

24068660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55744651-G-C

24068727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55744717-G-A

http://identifiers.org/hco/14/GRCh38#24068898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55744946-C-A

24068898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55744946-C-T

24069347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745345-G-A

http://identifiers.org/hco/14/GRCh38#24069539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55745534-A-C

24069539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55745534-A-G

24069646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55745634-T-C

24069646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55745634-T-G

http://identifiers.org/hco/14/GRCh38#24069727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#55745716-A-C

24069727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20272
most severe consequence: 3 prime UTR variant
orthologous variants: 55745716-A-T