57186210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95328488-T-A

57186210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95328488-T-C

57186229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95328507-T-A

57186261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, undefined
orthologous variants: 95328541-T-A

57186261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, undefined
orthologous variants: 95328541-T-C

57186261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, undefined
orthologous variants: 95328541-T-G

57186350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328631-C-T

57186404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328685-G-A

57186404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328685-G-C

57186404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328685-G-T

57186564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328850-C-T

57186565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328851-G-A

57186565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328851-G-T

http://identifiers.org/hco/16/GRCh38#57186621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95328907-C-A

57186621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95328907-C-T

57186644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328930-G-A

57186652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95328938-G-A

57186786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 95329059-G-T

57186804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95329073-T-C

57186890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95329153-G-T

57186916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 95329181-G-T

http://identifiers.org/hco/16/GRCh38#57187025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#95329321-C-A

57187134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329403-G-T

57187161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329438-C-T

57187201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95329478-A-G

http://identifiers.org/hco/16/GRCh38#57187224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95329501-A-C

57187344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329629-G-A

57187480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329767-C-G

57187489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95329778-A-G

57187812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95330021-G-C

57187913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330111-C-T

57188219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330365-G-A

57189468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330976-A-T

57189480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95330987-T-C

57189802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331293-G-A

57189834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331313-A-T

57190154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331704-G-C

57190291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95331917-C-T

57190700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332585-T-C

57190715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332600-A-G

57191080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95332862-A-G

57191588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95333736-C-T

57191868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95334206-G-A

57191868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95334206-G-T

57192193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95334537-G-A

57192366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95334704-A-G

57192499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95334846-A-G

57192674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335031-C-G

57193047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335651-A-G

57193167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95335769-C-T

57194223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337144-G-C

57194586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337470-A-G

57194705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337574-C-G

57194705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337574-C-T

57194773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337642-A-G

57194860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337728-T-C

57194860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95337728-T-G

57196057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338164-A-G

57196227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95338296-A-T

57196383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95338495-T-G

57196516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95338612-G-A

57196984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95338722-T-C

http://identifiers.org/hco/16/GRCh38#57197274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95339006-C-A

57198521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340305-C-G

57198650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340384-G-A

57199005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340746-C-T

57199010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95340750-C-G

57202876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342192-G-A

57202876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342192-G-T

57202877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342193-A-G

57202877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342193-A-T

57203476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342626-G-C

57203908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95342992-C-T

57204057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95348868-T-C

http://identifiers.org/hco/16/GRCh38#57204279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95349029-A-C

57204314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349068-A-G

57204338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349300-G-A

57204369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349329-T-C

57204452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349410-T-A

57204452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95349410-T-G

http://identifiers.org/hco/16/GRCh38#57204644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95349599-C-A

57204719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95349674-T-C

57204770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95349725-A-G

57204847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95349802-C-G

57204847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95349802-C-T

57205068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95350023-G-A

57205163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95350117-G-T

57205246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95350212-A-G

57205284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95350250-G-T

57205292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95350258-T-A

57205292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 95350258-T-C

57205496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95350460-A-G

57205531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95350494-C-G

57205534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95350497-C-T

57205723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95350670-C-T

http://identifiers.org/hco/16/GRCh38#57205845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95350757-A-C

57207524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95355167-T-G

57207631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 95355277-G-A

57207690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95355335-G-C

57207727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95355375-T-C

http://identifiers.org/hco/16/GRCh38#57207806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95355450-C-A

57207833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95355477-G-A

57208045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron variant
orthologous variants: 95355670-T-C

57208121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355747-T-C

57208240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355848-A-G

http://identifiers.org/hco/16/GRCh38#57208300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95355907-A-C

57208300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355907-A-T

57208359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355956-A-G

57208359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95355956-A-T

57209045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356348-C-T

57209166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 95356469-T-C

57209240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356544-T-C

http://identifiers.org/hco/16/GRCh38#57209250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95356554-C-A

57209250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356554-C-T

57209281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95356573-T-G

57211795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357450-G-T

57212075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357757-G-A

57212191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95357886-G-A

57212574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95358562-T-G

57212930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95358641-T-C

57212955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95358668-G-T

57213156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95358850-T-C

57213211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359209-T-A

57213217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359215-T-A

57213218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359216-G-A

57213247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359245-A-G

57213420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359375-A-G

57213532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359397-T-C

57213585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359442-G-A

57213619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359476-G-A

57213743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359594-G-A

57213743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359594-G-T

http://identifiers.org/hco/16/GRCh38#57213768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95359618-C-A

57213768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359618-C-T

57213801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95359646-A-T

http://identifiers.org/hco/16/GRCh38#57214254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95360119-C-A

http://identifiers.org/hco/16/GRCh38#57214273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95360220-A-C

57214280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95360227-G-A

57214280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95360227-G-T

57214991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95360908-G-A

57215346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361231-A-G

57215492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361368-T-A

57215492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361368-T-C

57215501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361377-G-A

57215619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361489-C-T

57215999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95361953-T-G

57216047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95362001-T-C

57216409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95362639-T-G

57216475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95362760-T-C

57216475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95362760-T-G

57216501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95362791-T-C

57216501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95362791-T-G

57216523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95362828-G-C

57216523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95362828-G-T

57216660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95362960-C-T

57216705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363003-G-A

57216772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363122-A-G

57216772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363122-A-T

http://identifiers.org/hco/16/GRCh38#57216801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95363151-C-A

57216801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363151-C-G

57216801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363151-C-T

http://identifiers.org/hco/16/GRCh38#57216833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95363181-C-A

57216833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363181-C-T

57216927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95363275-G-A

57216946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95363294-G-A

57216946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95363294-G-C

57217044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363392-G-C

57217044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363392-G-T

57217055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363403-T-C

57217081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363426-G-C

57217121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95363528-A-G

57217868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95364331-T-C

57220675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95364827-T-C

57220675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 95364827-T-G

http://identifiers.org/hco/16/GRCh38#57220874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95365025-C-A

http://identifiers.org/hco/16/GRCh38#57220915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95365064-C-A

57220915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95365064-C-T

57220935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95365673-G-T

57220985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95365716-T-A

57220999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95365730-T-A

57221128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95366020-G-A

57221128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95366020-G-T

http://identifiers.org/hco/16/GRCh38#57221197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95366080-C-A

http://identifiers.org/hco/16/GRCh38#57221198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95366081-C-A

57221198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95366081-C-T

http://identifiers.org/hco/16/GRCh38#57221802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95367077-A-C

57222012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95367383-C-T

57222024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95367395-T-C

57222870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95369472-G-A

57222967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95369536-G-A

57224162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370675-G-A

57224346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370829-A-G

57224389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370874-G-T

57224390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95370875-G-A

57224559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95371022-C-G

57224635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95371100-A-G

57224854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95371262-C-T

57227322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373192-T-A

http://identifiers.org/hco/16/GRCh38#57227327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95373197-C-A

57227327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373197-C-G

http://identifiers.org/hco/16/GRCh38#57227332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95373202-C-A

57227332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373202-C-G

57227332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373202-C-T

57227481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95373351-T-C

57230648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376329-G-T

http://identifiers.org/hco/16/GRCh38#57230655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376333-A-C

57230681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376352-A-G

57230712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 95376382-A-G

57230892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376557-C-G

57230892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376557-C-T

57230906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376571-A-G

57230963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376625-A-T

57231069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376734-G-T

http://identifiers.org/hco/16/GRCh38#57231080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376745-C-A

57231080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376745-C-T

http://identifiers.org/hco/16/GRCh38#57231097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376762-C-A

http://identifiers.org/hco/16/GRCh38#57231102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376767-C-A

http://identifiers.org/hco/16/GRCh38#57231106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376771-C-A

57231106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376771-C-G

57231106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376771-C-T

http://identifiers.org/hco/16/GRCh38#57231345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95376999-C-A

57231345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95376999-C-T

57231651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377887-T-G

57231671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95377907-G-A

57231830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378053-C-G

57232197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378599-G-T

57232294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378688-A-G

57232294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378688-A-T

57232319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378712-G-T

57232400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378920-A-G

57232435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95378962-A-G

57232813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95379280-G-A

57234794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380344-T-C

57234872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380408-C-T

http://identifiers.org/hco/16/GRCh38#57234999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95380740-C-A

57234999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380740-C-T

57235016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380757-A-T

57235059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380798-A-G

57235059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95380798-A-T

57235162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 95380893-G-A

57235342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95381120-A-G

57236150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382069-C-T

57236159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382079-G-A

57236238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382135-A-G

57236238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382135-A-T

57236362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382250-A-G

57236449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382370-A-G

57236457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95382378-A-G

http://identifiers.org/hco/16/GRCh38#57238815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95385273-C-A

57238815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385273-C-T

57238827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95385281-G-T

http://identifiers.org/hco/16/GRCh38#57239251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95385700-C-A

57239251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95385700-C-T

http://identifiers.org/hco/16/GRCh38#57239272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95385721-C-A

57239272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95385721-C-T

http://identifiers.org/hco/16/GRCh38#57239296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#95385745-C-A

57239296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95385745-C-T

57239817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95386255-A-T

57240272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29420
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 95386715-G-T