http://identifiers.org/hco/22/GRCh38#24806246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113458609-C-A

24806246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5 prime UTR variant
orthologous variants: 113458609-C-G

24806246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5 prime UTR variant
orthologous variants: 113458609-C-T

http://identifiers.org/hco/22/GRCh38#24806303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113458579-C-A

24806303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5 prime UTR variant
orthologous variants: 113458579-C-T

24806316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113458566-G-A

24806316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113458566-G-T

24806332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113458550-T-A

24806332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113458550-T-C

http://identifiers.org/hco/22/GRCh38#24806567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113458372-C-A

24806567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458372-C-T

24806571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458368-T-C

24806571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458368-T-G

24806584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458359-G-A

24806584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458359-G-T

24806733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113458285-C-T

24807103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457985-G-A

24807126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457966-C-T

24807169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457935-T-C

24807169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457935-T-G

24807570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457650-C-G

24807570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457650-C-T

24807658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457578-G-A

24807837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113457409-C-T

24808822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113456460-G-T

24808834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113456450-C-T

24808981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113456371-G-A

24809149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113456243-A-G

24809203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113456185-C-T

24810061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455635-G-A

24810061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455635-G-C

24810061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455635-G-T

24810144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455557-C-G

24810144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455557-C-T

24810176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455518-A-G

24810434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455274-T-C

http://identifiers.org/hco/22/GRCh38#24810455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113455253-C-A

24810455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113455253-C-T

24810771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113454940-G-A

24810989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113454748-G-C

24811039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113454698-A-T

24813003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113453255-C-T

24813104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113453167-G-A

24813148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113453138-G-A

24813148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113453138-G-C

24813460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113452740-A-G

24813513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113452698-G-C

24813586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113452558-G-T

24814996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113451164-C-T

http://identifiers.org/hco/22/GRCh38#24816125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113450560-A-C

24816822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113450182-G-A

24819930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113448637-G-A

24820012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113448570-G-C

24820476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113448155-A-G

24820489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113448144-G-C

24824501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445929-C-T

24824532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445906-T-G

24824612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445842-T-G

24824617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445836-C-G

24824667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445793-G-A

24824835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445643-A-G

24825890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445298-A-G

24825976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445213-C-G

24825976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445213-C-T

24826069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113445105-T-C

24827030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113444211-G-C

24827126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113444116-G-A

24827403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113443906-C-G

24827403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113443906-C-T

24827564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113443823-A-G

24827591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113443800-C-G

24834105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113439193-G-C

24834233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113439044-G-A

24843161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438329-G-A

24843212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438283-T-C

24843278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438225-T-G

24843285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438218-G-A

24843342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438171-A-G

24843360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438153-A-G

http://identifiers.org/hco/22/GRCh38#24843405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113438109-C-A

24843405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438109-C-G

24843405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438109-C-T

24843458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438066-A-G

24843459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron variant
orthologous variants: 113438065-T-C

http://identifiers.org/hco/22/GRCh38#24843463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113438061-C-A

24843497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113438041-G-A

24843497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113438041-G-T

http://identifiers.org/hco/22/GRCh38#24843597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113437951-C-A

24843597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437951-C-G

24843668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437883-G-A

24843668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437883-G-T

24843778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437781-T-A

24843778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437781-T-C

24843786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437773-T-C

24843818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437759-G-T

24843870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437729-T-C

24843870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437729-T-G

24843885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437718-G-C

24843885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437718-G-T

24844467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437112-G-A

24844467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437112-G-T

24844468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437111-A-G

24844468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437111-A-T

http://identifiers.org/hco/22/GRCh38#24844473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113437106-C-A

24844473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437106-C-T

24844476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437103-A-G

24844478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437101-A-G

24844533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437068-A-T

24844570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437049-T-A

24844570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437049-T-C

24844570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437049-T-G

24844584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437029-G-A

24844584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437029-G-C

24844584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437029-G-T

24844585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437028-G-A

24844585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437028-G-C

24844585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437028-G-T

24844596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437017-G-A

24844596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437017-G-T

24844598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437015-T-A

24844598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437015-T-C

24844598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113437015-T-G

24844616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436997-G-C

24844616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436997-G-T

24844620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436992-G-A

24844682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436955-T-C

24844682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436955-T-G

24844683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436954-G-C

24844683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436954-G-T

http://identifiers.org/hco/22/GRCh38#24844729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113436911-C-A

24844729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436911-C-T

http://identifiers.org/hco/22/GRCh38#24844818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113436845-C-A

24844818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436845-C-T

http://identifiers.org/hco/22/GRCh38#24844832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113436828-C-A

24844832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436828-C-T

http://identifiers.org/hco/22/GRCh38#24844833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113436827-A-C

24844833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436827-A-T

http://identifiers.org/hco/22/GRCh38#24844847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113436806-C-A

24844847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436806-C-G

24844876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113436779-C-T

24844997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113436652-G-A

24845080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113436558-T-C

24847613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113435272-C-G

24847613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113435272-C-T

24847628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113435257-C-G

24847628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113435257-C-T

24847648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113435237-T-C

24847705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113435180-G-A

24847744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113435141-G-A

24847824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113435064-G-A

24847824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113435064-G-C

24850246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434823-G-A

24850256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434815-T-C

http://identifiers.org/hco/22/GRCh38#24850332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113434739-C-A

24850332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113434739-C-T

24850356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113434715-A-G

24850383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113434688-T-A

24850450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113434628-G-A

24850494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113434588-A-G

http://identifiers.org/hco/22/GRCh38#24850515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113434568-C-A

24850515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434568-C-T

24850518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434565-C-T

24850532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434544-T-A

24850532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434544-T-C

24850534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434542-G-C

24850534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434542-G-T

24850672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434364-T-C

24850673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113434363-T-C

24853424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433977-T-G

24854322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433773-A-G

24855249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433323-G-A

24855255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433317-G-A

24855255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433317-G-C

24855350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113433223-G-A

24855350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113433223-G-C

24855447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433126-G-A

24855451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113433122-G-A

24855691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113432836-A-G

24855691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113432836-A-T

24855708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113432819-T-C

24855856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113432663-T-A

24856042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113432425-C-T

24856622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113431774-C-G

24856741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113431659-A-G

24859621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430670-G-A

24859621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430670-G-T

24859882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430413-C-T

24859888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430407-T-G

http://identifiers.org/hco/22/GRCh38#24859981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113430334-C-A

24859981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430334-C-T

24860002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113430313-G-A

24865893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113429391-G-A

24865897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113429387-G-A

24865905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113429379-G-A

24866219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113429084-T-G

24866293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113429003-G-A

24866343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428940-A-G

24866556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428725-A-G

24866768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428547-C-T

24866864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428422-G-A

http://identifiers.org/hco/22/GRCh38#24866975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113428320-C-A

24866975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428320-C-T

24867030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428292-G-A

24867030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428292-G-T

24867203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428148-G-T

24867215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428131-G-A

24867236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428109-T-C

http://identifiers.org/hco/22/GRCh38#24867243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113428101-C-A

24867243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428101-C-T

http://identifiers.org/hco/22/GRCh38#24867270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113428089-C-A

24867270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428089-C-T

http://identifiers.org/hco/22/GRCh38#24867300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113428065-C-A

24867300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428065-C-T

http://identifiers.org/hco/22/GRCh38#24867306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113428059-C-A

24867306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113428059-C-T

24867681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427824-G-A

24867766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427792-C-G

24867766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427792-C-T

24867898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427663-A-G

24868084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427599-C-T

24868085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427598-G-A

24868085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427598-G-T

24868355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427507-T-C

http://identifiers.org/hco/22/GRCh38#24868360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113427500-C-A

24868360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427500-C-T

24868544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427316-G-C

24868547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113427313-A-T

24868568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427290-T-C

24868653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427197-A-G

24868653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113427197-A-T

24868717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113427135-T-C

24868768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113427084-G-T

24868795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113427057-G-T

24868798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113427054-G-C

24868798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113427054-G-T

24868945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113426919-C-T

http://identifiers.org/hco/22/GRCh38#24868992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113426876-C-A

24869185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113426676-C-G

24869185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113426676-C-T

24869194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113426669-T-A

http://identifiers.org/hco/22/GRCh38#24874285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113425665-A-C

24874285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425665-A-T

24874289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425661-G-A

24874289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425661-G-T

24874293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425657-G-A

24874293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425657-G-T

http://identifiers.org/hco/22/GRCh38#24874349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113425601-C-A

24874349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425601-C-G

24874389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425563-T-C

http://identifiers.org/hco/22/GRCh38#24874548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113425404-C-A

24874607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425348-G-A

24874607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425348-G-C

24874664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425295-G-T

24874714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425238-G-A

24874714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425238-G-C

24874714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425238-G-T

http://identifiers.org/hco/22/GRCh38#24874724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113425228-C-A

24874854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425173-G-T

24874962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425096-T-C

24875003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425055-G-A

24875003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425055-G-C

24875008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113425050-G-A

24875119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113424957-T-G

24876306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113424333-T-G

24876547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113424072-T-C

24876547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113424072-T-G

24876940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423665-G-C

24876975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423638-C-T

24878383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423291-C-T

24878443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423252-A-G

24878443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423252-A-T

24878617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423072-C-T

24878620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423069-T-C

24878650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113423046-C-G

http://identifiers.org/hco/22/GRCh38#24879334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113422324-C-A

24879334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422324-C-T

http://identifiers.org/hco/22/GRCh38#24879349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113422317-C-A

24879349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422317-C-G

24879363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422304-T-C

http://identifiers.org/hco/22/GRCh38#24879368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113422299-C-A

24879368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422299-C-G

24879368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422299-C-T

24879419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113422252-G-A

24883508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421808-G-A

24883982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421658-G-T

24883983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421657-G-A

24883983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421657-G-T

24884154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113421487-G-A

24884208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421439-A-T

24884283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421381-T-G

24884292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421372-T-G

http://identifiers.org/hco/22/GRCh38#24884297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113421367-C-A

24884297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113421367-C-T

24886606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113416687-G-A

24886744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416550-T-A

24886744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416550-T-C

http://identifiers.org/hco/22/GRCh38#24886748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113416546-C-A

24886748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416546-C-G

24886748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416546-C-T

24886765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416513-A-G

24886765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416513-A-T

24886785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416494-T-C

24886785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113416494-T-G

24893416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414346-C-G

24893431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 113414333-G-A

24893470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113414294-G-T

24893488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113414276-G-A

24893488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 113414276-G-T

http://identifiers.org/hco/22/GRCh38#24893632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113414131-C-A

24893632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414131-C-T

24893642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414121-G-A

24893642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414121-G-T

24893655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414111-G-A

24893655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414111-G-T

http://identifiers.org/hco/22/GRCh38#24893724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113414091-C-A

24893836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113414004-T-C

24895114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113413907-T-C

24895114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113413907-T-G

http://identifiers.org/hco/22/GRCh38#24895148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113413872-C-A

24895189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113413845-C-T

http://identifiers.org/hco/22/GRCh38#24895313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113413704-C-A

24895353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113413628-G-A

24895353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113413628-G-T

http://identifiers.org/hco/22/GRCh38#24895380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113413601-C-A

http://identifiers.org/hco/22/GRCh38#24897852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113411816-C-A

24897852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411816-C-G

24897852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411816-C-T

24897878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411790-G-T

24897881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411787-G-A

24897881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411787-G-C

24897928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113411743-A-G

24897972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 113411700-G-A

24898035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411637-C-T

24898131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411541-T-A

24898161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411511-G-A

24898185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411487-C-G

24898186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411486-C-G

http://identifiers.org/hco/22/GRCh38#24898188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113411484-A-C

24898213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411459-G-A

24898245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411427-A-G

24898254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411418-G-T

24898266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411406-C-G

24898266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411406-C-T

24898382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113411290-T-C

24898413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411262-A-T

24898455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113411220-G-A

24901696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113408115-C-T

24901700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113408111-T-A

24901735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113408098-G-A

24901735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113408098-G-T

24901790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113408070-T-G

http://identifiers.org/hco/22/GRCh38#24901805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113408055-C-A

24901872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113407998-A-T

http://identifiers.org/hco/22/GRCh38#24901899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113407971-C-A

24901899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113407971-C-T

24901920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113407950-C-T

24901967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407897-G-T

24901970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407894-A-G

24901978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407886-G-A

24901978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407886-G-T

http://identifiers.org/hco/22/GRCh38#24901979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113407885-A-C

24901990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407874-G-A

24901990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407874-G-T

24901997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407866-G-A

24901997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407866-G-T

24901998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407865-T-A

24901998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407865-T-C

24901998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407865-T-G

24902013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407850-G-A

24902013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407850-G-T

24902015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407848-G-A

24902015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113407848-G-T

24904862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406940-A-G

24904939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406878-G-C

24904974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406847-G-A

24904974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406847-G-T

24904997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406825-G-A

24905010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406817-G-T

24905106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 113406736-T-A

24905127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113406715-A-T

24905133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113406709-T-C

24905163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113406679-C-G

24905163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113406679-C-T

24905166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113406676-C-T

24905175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113406667-A-G

http://identifiers.org/hco/22/GRCh38#24905239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113406632-C-A

24905239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406632-C-G

24905323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406549-T-C

24905335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406537-T-A

24905389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406491-G-T

24905414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406470-A-G

24905890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406089-A-G

24905891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406088-A-G

24905969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113406019-A-G

24906074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113405916-G-A

24906141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113405849-T-G

http://identifiers.org/hco/22/GRCh38#24912621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113403248-C-A

24912708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113403160-G-T

24912803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113403071-T-A

24917333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401210-T-G

24917521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401075-T-C

24917548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401050-G-C

24917548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401050-G-T

24917553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401045-G-A

24917553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401045-G-T

http://identifiers.org/hco/22/GRCh38#24917556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113401042-C-A

24917556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401042-C-T

24917563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401035-G-T

http://identifiers.org/hco/22/GRCh38#24917584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113401014-C-A

24917584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401014-C-T

http://identifiers.org/hco/22/GRCh38#24917595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113401003-C-A

24917595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113401003-C-T

24917673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113400943-C-T

24917736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 113400880-C-T

24917763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113400855-T-G

24917794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113400832-G-A

24917810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113400816-G-T

24919398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113399233-A-G

24919411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113399220-G-A

24919411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113399220-G-T

24919471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113399163-G-A

24919689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113399029-T-C

http://identifiers.org/hco/22/GRCh38#24919731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113398998-C-A

24919734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398995-G-A

24919734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398995-G-T

24919806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398923-G-A

24919806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398923-G-T

24919879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113398851-C-G

24919879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113398851-C-T

24919918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113398812-G-C

24919924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113398806-G-A

24920020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398700-G-A

24920130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398502-G-T

24920595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113398139-C-T

24920668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113397983-G-A

24920778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113397882-G-A

24921621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393978-G-A

24921621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393978-G-C

24921626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393973-T-C

24923406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393520-G-A

24923450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393482-T-A

24923645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393364-G-A

24924044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393091-G-A

24924044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393091-G-T

24924046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393089-T-C

24924046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393089-T-G

24924125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393025-A-G

http://identifiers.org/hco/22/GRCh38#24924133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113393017-C-A

24924133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393017-C-G

24924133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393017-C-T

24924137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393013-G-A

24924137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113393013-G-T

24924142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113392996-G-T

24924206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113392937-A-G

24924310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392847-C-G

http://identifiers.org/hco/22/GRCh38#24924315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392842-C-A

24924315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392842-C-T

24924389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392798-G-T

http://identifiers.org/hco/22/GRCh38#24924404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392783-C-A

24924404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392783-C-G

24924404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392783-C-T

24924681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392569-G-T

24924695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392555-G-T

24924715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392535-T-G

24924793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392454-G-A

24924793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392454-G-C

24924793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392454-G-T

24924853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392425-T-A

24924853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392425-T-C

24924853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392425-T-G

http://identifiers.org/hco/22/GRCh38#24924863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392415-C-A

24924863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392415-C-T

http://identifiers.org/hco/22/GRCh38#24924876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392413-C-A

24924876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392413-C-T

http://identifiers.org/hco/22/GRCh38#24924879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392410-C-A

24924879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113392410-C-G

24925451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392212-T-C

24925513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392162-G-T

24925514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392161-G-A

http://identifiers.org/hco/22/GRCh38#24925547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392127-C-A

http://identifiers.org/hco/22/GRCh38#24925633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113392069-C-A

24925651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392050-A-G

24925699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392007-T-G

24925706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113392000-A-G

24925721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391986-T-C

24925724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391983-G-A

24925724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391983-G-T

24925760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391948-G-T

24925816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391904-G-T

24925838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391887-A-G

24925839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391886-T-C

24925983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391773-G-A

24925983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391773-G-T

24926016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391747-A-G

http://identifiers.org/hco/22/GRCh38#24926218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113391629-C-A

24926218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391629-C-T

24926244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391610-C-T

24926287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391593-G-A

24926287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391593-G-T

24926301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391571-T-C

24926386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391509-A-G

24926397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391490-G-A

24926416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391473-C-G

24926459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391438-G-A

24926459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391438-G-T

http://identifiers.org/hco/22/GRCh38#24926523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113391385-C-A

24926646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391272-T-A

24926688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391237-G-T

24926722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391203-G-A

24926722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391203-G-C

24926722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391203-G-T

24926742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391175-G-A

24926742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391175-G-T

24926743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391174-G-A

24926780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29410
most severe consequence: 3 prime UTR variant
orthologous variants: 113391142-G-T