223220870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 182724113-C-G

223220870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 182724113-C-T

223221213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723722-A-G

223221291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723646-T-C

http://identifiers.org/hco/1/GRCh38#223221413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182723531-C-A

223221468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723479-G-T

223221538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723421-T-C

223221547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723412-G-A

223221679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723295-T-C

223221795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723166-T-C

223221841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723121-A-G

223221841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723121-A-T

223221892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182723086-A-G

http://identifiers.org/hco/1/GRCh38#223222104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182722871-C-A

223222104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182722871-C-T

223222196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 182722786-G-A

http://identifiers.org/hco/1/GRCh38#223222723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182722310-C-A

223222960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182720054-G-A

223223114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719901-T-C

223223117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719898-G-A

223223117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719898-G-C

223223117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719898-G-T

223223151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719865-G-A

223223151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719865-G-C

223223151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719865-G-T

223223156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719860-G-A

223223156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719860-G-C

223223156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719860-G-T

223223320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 182719757-T-A

223223320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 182719757-T-C

223223431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 182719646-T-A

223223657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719421-A-G

223224384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719335-G-A

223224510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182719211-A-T

223224591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182719112-T-C

223224602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182719101-G-T

223225869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182718291-G-A

http://identifiers.org/hco/1/GRCh38#223225914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182718246-C-A

223225916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182718244-T-C

223226318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717796-T-C

223226343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717771-C-G

223226417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717718-C-T

223226522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717627-G-A

223226774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717476-C-T

223226896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717460-C-G

223227146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717272-G-A

223227146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717272-G-T

http://identifiers.org/hco/1/GRCh38#223227268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182717180-C-A

223227273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717175-G-A

223227374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717080-G-A

http://identifiers.org/hco/1/GRCh38#223227383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182717072-C-A

223227383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182717072-C-T

http://identifiers.org/hco/1/GRCh38#223227841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182716280-C-A

223227841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182716280-C-T

223227885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182716240-G-A

223227937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182716193-C-T

223227976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182716109-T-G

223228110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715984-G-C

223228431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715722-C-T

223228646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715490-T-C

223228796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715371-C-T

223228922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715288-C-T

223229081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715211-G-A

223229081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715211-G-T

223229180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715111-G-A

223229180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715111-G-C

223229180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182715111-G-T

223229442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 182714853-G-T

223229472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182714817-G-T

223229738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182714570-A-T

http://identifiers.org/hco/1/GRCh38#223229975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182714314-C-A

223230102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182714207-C-T

223230108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182714198-T-A

223230305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182714008-C-T

http://identifiers.org/hco/1/GRCh38#223230352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182713963-C-A

223230374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182713939-A-G

http://identifiers.org/hco/1/GRCh38#223230486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182713828-C-A

223230486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182713828-C-T

223230644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 182713700-C-T

223230720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 182713630-T-A

223230730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 182713620-A-G

223230776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182713575-G-A

223230797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182713554-A-G

http://identifiers.org/hco/1/GRCh38#223230800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182713551-C-A

http://identifiers.org/hco/1/GRCh38#223231049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182713361-C-A

223231049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182713361-C-G

223231049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182713361-C-T

223231194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182713241-G-A

223231268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182713218-G-A

223231324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182713159-A-G

223231553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182712918-A-T

223231681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182712815-G-A

223233031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182711370-C-T

223233037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182711365-C-G

223233125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182711268-C-T

223233216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182711183-C-T

223233731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182710400-G-A

223233839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182710237-T-C

223233938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182710126-C-T

223234052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182710005-C-T

223234146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709918-A-G

223234170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709895-A-G

223234170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709895-A-T

223234240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709822-C-T

223234264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709805-C-T

223242741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709435-G-A

223242869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709316-G-A

http://identifiers.org/hco/1/GRCh38#223243108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182709087-A-C

223243197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709012-T-C

223243202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182709007-G-A

223243231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182708976-C-T

223243235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182708972-C-T

223243321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182708900-G-A

223243564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182708347-G-A

223243745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182708197-A-G

http://identifiers.org/hco/1/GRCh38#223244243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182707832-C-A

223244358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182707738-G-T

223245005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182706779-C-T

223245254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182706570-A-G

http://identifiers.org/hco/1/GRCh38#223246905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182704957-A-C

223246930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182704937-G-A

223247030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182704888-G-A

223247047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182704872-T-G

http://identifiers.org/hco/1/GRCh38#223247394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182704532-C-A

223247728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182704212-C-T

223247828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182704110-C-T

223248109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703816-C-T

223248219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703728-G-A

223248507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703459-G-A

223248885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703082-T-C

223248952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703019-C-T

223248953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182703018-G-A

223249126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182702870-G-A

223249258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182702744-G-A

223249413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182702566-G-A

223253637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182699909-C-T

223254013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182699560-G-A

223254040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182699534-G-C

223254370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182699330-C-T

223254417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182698429-G-C

223254497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182698353-A-G

223254500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182698350-T-C

223255509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182696954-C-T

223255616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182696850-A-G

http://identifiers.org/hco/1/GRCh38#223255653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182696813-C-A

223255723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182696747-A-G

223255850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182696608-T-C

223256459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695997-A-G

223256496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695965-G-A

223256643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695835-G-C

223256720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695773-C-G

http://identifiers.org/hco/1/GRCh38#223256732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182695769-C-A

223257015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695609-C-T

223257046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695581-T-C

223257106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695539-T-C

223257225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695424-T-G

223257230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695419-G-A

223257241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695406-T-C

223257313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182695339-G-A

223257757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182694884-C-T

223257870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182694781-A-T

223257993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182694677-G-A

223258113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182694527-T-A

http://identifiers.org/hco/1/GRCh38#223258874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182693743-C-A

223258874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693743-C-T

223258882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693735-A-G

223258929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693689-A-G

http://identifiers.org/hco/1/GRCh38#223258948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182693670-A-C

223259090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693606-G-A

223259106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693590-G-C

223259329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182693363-G-T

223259448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182691060-C-T

223259849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690631-C-T

223259908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690575-G-A

223260058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690451-T-C

223260058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690451-T-G

223260074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690436-T-C

223260175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690337-G-T

223260269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690248-T-C

223260304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690214-A-G

223260312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690206-T-A

223260442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182690068-A-G

223260586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689959-G-T

http://identifiers.org/hco/1/GRCh38#223260588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182689957-C-A

223260827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689883-G-A

223261026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689746-T-A

223261146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689640-C-T

223261347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689456-A-G

http://identifiers.org/hco/1/GRCh38#223261505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182689321-A-C

223261713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182689049-T-C

http://identifiers.org/hco/1/GRCh38#223261772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182688909-A-C

http://identifiers.org/hco/1/GRCh38#223262150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182688386-C-A

http://identifiers.org/hco/1/GRCh38#223262163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182688373-A-C

223262299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182688270-C-G

223262376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182688195-T-A

223262704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687978-T-A

223262859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687823-C-T

223262919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687765-A-G

223263160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687501-T-C

223263222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687430-C-T

223263521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687163-T-A

223263521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687163-T-C

223263580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687103-A-G

223263673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182687006-T-C

223263702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686963-A-G

223263794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686870-T-C

223263846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686837-A-G

223263870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686813-G-A

223263913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686789-C-T

223263922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686781-C-G

223263922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686781-C-T

223263974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686742-G-T

223264000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686717-C-T

223264109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686636-T-C

223264207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686539-A-T

223264211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686535-A-G

223264256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686490-A-G

http://identifiers.org/hco/1/GRCh38#223264265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182686481-C-A

223264265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686481-C-G

223264265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182686481-C-T

223264391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182686353-C-G

223264391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 182686353-C-T

223264416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182686326-C-T

223264519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182686240-T-C

223264519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182686240-T-G

223264533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182686223-T-A

223264533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182686223-T-C

223264659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 182686144-G-C

223264827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182685983-G-A

223264878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182685931-G-A

223264878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182685931-G-T

223264891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 182685918-C-T

http://identifiers.org/hco/1/GRCh38#223264895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#182685914-A-C

223264932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685893-G-A

223264932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685893-G-T

http://identifiers.org/hco/1/GRCh38#223265096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182685760-C-A

http://identifiers.org/hco/1/GRCh38#223265231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182685575-A-C

223265439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685396-T-C

223265499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685333-G-T

223265544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685304-C-T

223265744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685126-T-A

223265744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685126-T-C

223265824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685044-G-A

223265824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182685044-G-T

223265905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684963-T-C

223265949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684921-C-G

223266055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684835-G-A

223266055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684835-G-T

223266168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684733-G-A

223266202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684703-C-T

223266297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684288-T-C

223266332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684254-G-A

http://identifiers.org/hco/1/GRCh38#223266362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182684225-A-C

223266378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684209-A-G

223266412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684173-G-A

223266467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182684126-T-A

223266569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683913-T-C

223266685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683795-C-T

223266686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683794-A-G

223266792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683688-C-T

223266910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683578-G-A

223267079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683407-G-T

223267144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182683260-C-T

223267449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682828-C-T

223267680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682618-G-A

223267690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682608-C-T

223267760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682538-T-C

223267796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682502-T-A

223268080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682245-G-T

223268107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182682220-T-C

223268234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681907-T-G

223268390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681787-T-C

223268414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681764-T-A

223268414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681764-T-C

223268419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681759-T-G

http://identifiers.org/hco/1/GRCh38#223268447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182681727-A-C

223268491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681704-C-T

223268537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 182681658-T-C

223268540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 182681655-C-T

223268636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 182681559-T-C

http://identifiers.org/hco/1/GRCh38#223268731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182681475-C-A

223268743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681463-A-G

223268765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681437-T-G

223268821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681381-G-T

http://identifiers.org/hco/1/GRCh38#223268917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182681313-A-C

223268949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681281-G-A

223269048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182681225-G-A

223269516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680863-G-T

223269640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680608-A-G

223269734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680512-T-C

223269947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680304-G-A

223269954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680297-G-A

223270014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680254-A-T

223270088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680202-T-C

223270264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680059-G-A

223270303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182680012-C-T

http://identifiers.org/hco/1/GRCh38#223271062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182679579-C-A

223271086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182679555-C-T

223271294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182679344-A-G

http://identifiers.org/hco/1/GRCh38#223271295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182679343-C-A

223271615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182679068-C-T

223271695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182678989-A-G

223271714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182678970-T-C

223271735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182678948-G-A

223272797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182677502-G-C

223273238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182677065-C-T

223273815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676642-C-T

223273908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676563-T-C

223273999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676493-G-T

http://identifiers.org/hco/1/GRCh38#223274069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182676435-C-A

223274089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676415-T-C

223274245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676305-C-G

223274312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676238-A-G

223274324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676226-G-A

http://identifiers.org/hco/1/GRCh38#223274492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182676065-C-A

223274492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676065-C-T

223274525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182676031-A-G

223274661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182675762-A-T

223274690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182675737-A-G

223274965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182675466-G-A

223275205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182670647-C-T

223275211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182670641-C-T

223275462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182670012-G-C

223275669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669708-G-A

223275689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669682-T-C

223275705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669667-T-C

223275757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669638-A-T

223276177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669265-G-T

223276196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669251-C-T

223276283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669162-T-C

223276302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669143-C-T

223276309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669136-A-G

223276358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669081-G-A

223276378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182669060-C-T

223276551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668873-G-A

223276732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668699-G-A

223276808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668627-C-T

223277012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668422-G-A

223277315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668131-T-C

223277388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182668053-A-G

223277957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182667561-G-A

223284279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182667395-G-A

223284304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182667370-G-T

223285212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666954-T-C

223285214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666951-G-A

223285342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666844-G-A

223286685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666428-T-C

223286699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666407-C-T

223286722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666384-G-C

223286722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666384-G-T

223286744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666362-A-G

223286784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666338-T-C

223286808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666313-T-C

223286828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182666296-A-G

223287692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182665566-A-G

223287752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182665502-T-C

http://identifiers.org/hco/1/GRCh38#223287919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182665342-A-C

223287998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182665267-C-T

http://identifiers.org/hco/1/GRCh38#223289010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182664766-A-C

223289087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664689-G-A

223289087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664689-G-T

223289138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664653-G-A

223289377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664430-T-C

http://identifiers.org/hco/1/GRCh38#223289384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182664423-A-C

223289384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664423-A-T

223289425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664376-G-T

223289469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182664310-G-A

223289621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182663971-G-A

223289622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182663970-T-C

223290229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182662725-T-C

223290334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182662585-T-A

223290334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182662585-T-C

223290462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182662380-C-T

http://identifiers.org/hco/1/GRCh38#223290613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182662250-C-A

http://identifiers.org/hco/1/GRCh38#223290625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182662243-C-A

223290625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182662243-C-G

223291009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661911-C-T

223291701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661434-A-T

223291725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661415-A-G

223291735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661405-T-C

223291739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661401-G-A

223291896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661233-A-G

223291945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661198-G-A

223292099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661079-C-T

223292162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661027-G-A

223292171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182661019-T-C

223292203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182660988-T-C

223292296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182660908-T-C

http://identifiers.org/hco/1/GRCh38#223292380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182660884-C-A

223292528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 182660749-A-G

223292657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 182660608-T-A

223292657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 182660608-T-G

http://identifiers.org/hco/1/GRCh38#223292709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182660584-C-A

223292709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660584-C-G

223292709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660584-C-T

223292797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660492-G-A

223294251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660237-G-A

223294251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660237-G-T

223294339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182660181-A-G

223297114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182659516-C-G

http://identifiers.org/hco/1/GRCh38#223297258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182659399-C-A

223297258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182659399-C-T

223297324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182659352-G-A

223297712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658835-C-T

223297827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658724-T-C

http://identifiers.org/hco/1/GRCh38#223297869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182658681-A-C

223297869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658681-A-G

223298017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658529-G-C

http://identifiers.org/hco/1/GRCh38#223298222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182658209-C-A

223298223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658208-T-C

223298273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658165-G-T

223298346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182658104-C-T

223298579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182657743-G-A

223298682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182657654-A-T

223298750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182657578-T-C

http://identifiers.org/hco/1/GRCh38#223299380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182656997-C-A

223299571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656806-T-C

223299639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656722-G-A

223299842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656508-T-G

223300142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656195-G-A

223300207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656128-A-G

223300223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656110-C-T

223300229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656104-A-T

223300306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182656027-C-T

http://identifiers.org/hco/1/GRCh38#223300352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182655979-A-C

223301115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182655326-A-T

http://identifiers.org/hco/1/GRCh38#223301121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182655320-A-C

223301329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182655152-T-A

223301430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182655054-A-T

223301564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654916-C-T

223301575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654905-C-T

223301635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654845-T-C

223301635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654845-T-G

223301662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654806-T-C

http://identifiers.org/hco/1/GRCh38#223301735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182654733-A-C

223302468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654278-G-T

223302479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654267-C-T

223302532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654211-T-G

223302612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654129-G-A

http://identifiers.org/hco/1/GRCh38#223302617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182654124-C-A

223302617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654124-C-G

223302759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182654058-T-A

223303208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653885-A-G

223303401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653690-C-T

223303403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653688-T-C

223304447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653327-C-T

223304501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653272-G-A

223304612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653159-A-G

http://identifiers.org/hco/1/GRCh38#223304665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182653108-C-A

223304698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182653075-G-A

http://identifiers.org/hco/1/GRCh38#223304846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182652902-A-C

223304846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652902-A-G

223304846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652902-A-T

223304855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652866-T-A

223304855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652866-T-C

http://identifiers.org/hco/1/GRCh38#223304872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182652844-A-C

223304872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652844-A-G

223304872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652844-A-T

223304942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652778-C-T

223304950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652770-T-C

223304967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652749-G-C

223305180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652554-C-T

223305238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652489-C-T

http://identifiers.org/hco/1/GRCh38#223305460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182652285-C-A

223305619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652103-T-C

223305704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182652017-A-G

223305790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651927-T-A

223305790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651927-T-C

223305790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651927-T-G

223305868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651849-C-T

223305873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651844-A-T

223306156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651566-C-T

223306279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651443-T-G

223306289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651433-C-T

http://identifiers.org/hco/1/GRCh38#223306297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182651425-A-C

223306319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651408-A-G

223306401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651329-T-C

http://identifiers.org/hco/1/GRCh38#223306861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182651154-C-A

223306861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651154-C-T

223306866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182651149-T-C

223307535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182650360-T-C

http://identifiers.org/hco/1/GRCh38#223307861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182649518-C-A

223307867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649516-C-T

223308074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649269-T-C

http://identifiers.org/hco/1/GRCh38#223308698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182649120-A-C

223308742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649078-T-C

223308742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649078-T-G

223308837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649008-A-G

223308843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182649002-G-A

http://identifiers.org/hco/1/GRCh38#223308913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182648941-A-C

223309040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648806-A-G

223309273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648560-T-A

223309440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648436-G-A

223309535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648345-G-C

223309577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648308-C-T

223309578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648307-C-T

223309643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648245-T-A

223309671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648217-G-A

223309687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648201-C-T

http://identifiers.org/hco/1/GRCh38#223309718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182648175-A-C

223309793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182648108-C-G

223310444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182647499-T-C

223310444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182647499-T-G

223310806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646953-G-A

223311099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646637-G-A

223311119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646623-C-T

223311200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646567-C-T

223311312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646464-C-G

223311415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646352-C-T

223311503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646278-T-C

223311525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182646256-T-A

http://identifiers.org/hco/1/GRCh38#223311796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182645976-C-A

223312144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182645668-T-A

223312173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182645639-C-T

http://identifiers.org/hco/1/GRCh38#223312174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182645638-A-C

223312314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182645498-G-C

223312493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182645318-T-C

http://identifiers.org/hco/1/GRCh38#223312514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182645297-C-A

223312848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182644971-C-G

223315718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182644138-T-C

223315883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643975-T-C

223316072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643778-T-C

223316098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643752-A-T

http://identifiers.org/hco/1/GRCh38#223316246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182643470-A-C

223316296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643422-A-G

223316411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643192-T-C

223316477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643107-C-T

223316511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182643066-T-C

223316685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642891-G-A

223316757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642853-G-C

223316880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642720-G-C

223316922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642678-G-C

223316923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642677-G-A

223316936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642663-G-C

223317552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642592-G-A

223319526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642268-G-T

223319551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642243-C-G

223319562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642232-C-G

223319736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182642096-A-G

223319903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641928-A-G

223320013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641820-C-T

223320058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641772-G-T

223320286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641613-G-T

223320366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641542-T-G

223320430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641483-G-A

223320430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641483-G-C

http://identifiers.org/hco/1/GRCh38#223320516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182641428-A-C

223320597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182641017-G-T

http://identifiers.org/hco/1/GRCh38#223320666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182640942-C-A

223320811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640821-A-T

223320958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640675-G-A

223321008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640640-C-T

223321019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640629-C-G

http://identifiers.org/hco/1/GRCh38#223321285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182640383-C-A

223321286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640382-C-G

223321408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182640250-C-T

http://identifiers.org/hco/1/GRCh38#223321708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182639966-C-A

223322650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638932-G-A

http://identifiers.org/hco/1/GRCh38#223322730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182638877-C-A

223322730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638877-C-T

223322932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638672-C-T

223323271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638404-G-A

223323274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638401-G-A

223323552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638279-T-C

223323607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638234-G-C

223323713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638191-C-T

223323723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638183-A-G

223323724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638182-G-A

http://identifiers.org/hco/1/GRCh38#223323725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182638181-C-A

223323916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182638052-A-G

223324081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182637907-C-T

http://identifiers.org/hco/1/GRCh38#223324325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182637752-C-A

223324325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182637752-C-G

223324418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182637679-A-G

223324679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182635103-T-G

223324940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634940-G-A

223324977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634906-T-C

223324977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634906-T-G

223325146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634757-T-A

223325166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634737-C-T

223325188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634716-C-T

223325433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182634145-T-C

http://identifiers.org/hco/1/GRCh38#223327499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182634099-A-C

223327659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633926-G-A

223328138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633502-C-G

223328245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633380-C-T

223328252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633370-T-C

223328605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633115-C-T

223328614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182633106-C-T

223329158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632600-T-C

223329207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632390-A-G

223329223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632374-T-C

223329284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632310-C-T

223329343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632249-C-T

223329522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632086-T-A

223329522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632086-T-C

223329585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182632031-T-A

http://identifiers.org/hco/1/GRCh38#223329590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182632026-C-A

http://identifiers.org/hco/1/GRCh38#223329604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182632012-A-C

223330133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182631811-A-G

223330181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182631763-C-T

223330311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182631633-A-G

223330418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630871-T-A

223330488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630801-G-A

223330518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630771-A-G

http://identifiers.org/hco/1/GRCh38#223330585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182630705-C-A

223330585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630705-C-T

223330657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630633-G-A

223330657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630633-G-C

223330671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630619-A-G

223330779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630511-T-C

223330910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630380-A-T

223330912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630378-G-T

223330960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630329-T-C

223331169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630195-T-C

223331266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630099-G-T

223331294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630068-A-G

223331354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630009-G-A

223331354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182630009-G-T

223331491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629872-G-A

223331733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629646-G-A

223331733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629646-G-C

223331733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629646-G-T

223331778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629607-G-A

223331828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629557-T-A

223331879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629505-A-G

223331902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629482-T-C

223331931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629432-C-T

223331989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629388-C-T

223332029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629347-G-C

223332072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629311-C-T

223332106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629241-T-A

223332244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629103-T-C

223332303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629044-A-G

223332342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182629005-T-C

223332401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182628947-T-C

223332402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182628946-T-C

223332408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182628940-G-A

223332408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182628940-G-C

223335515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182627603-G-C

223336364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182625707-G-A

223336387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182625684-T-A

223336527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182625567-A-T

223336912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182625247-A-G

223337422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624953-G-A

223337636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624732-C-T

223337894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624536-C-T

223338012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624415-G-T

223338028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624399-C-T

223338289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182624156-C-T

223338766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182623221-T-C

223338772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182623217-T-A

223339257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182622419-G-C

223339478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182622230-G-A

223339633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182622087-C-T

223339672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182622054-A-G

223339759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621975-C-T

223339772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621962-C-T

223339802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621931-G-C

223339804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621929-A-G

223339822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621911-G-A

223339925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621804-G-C

223340149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621614-G-A

223340149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621614-G-C

223340149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621614-G-T

223340151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621612-C-G

http://identifiers.org/hco/1/GRCh38#223340598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182621208-C-A

223340598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621208-C-G

223340598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621208-C-T

223340643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621170-T-A

223340643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621170-T-C

223340643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621170-T-G

223340662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621150-G-T

223340700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182621119-G-A

http://identifiers.org/hco/1/GRCh38#223340764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182621056-A-C

http://identifiers.org/hco/1/GRCh38#223341453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182620411-A-C

223341523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182620350-C-T

223341854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182620119-A-T

223341863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182620110-C-T

http://identifiers.org/hco/1/GRCh38#223341887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182620073-A-C

223341931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182620029-T-G

223341946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182620016-A-G

223342000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619968-A-G

223342192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619816-G-A

223342241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619767-G-A

223342241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619767-G-T

223342256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619752-A-G

223342293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619715-T-C

223342370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619638-G-A

223342614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619395-T-C

223342944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182619074-T-C

223343176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182618073-A-T

223343327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182617958-C-T

223343605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182617680-G-A

223343605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182617680-G-C

223343605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182617680-G-T

http://identifiers.org/hco/1/GRCh38#223343938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182617404-A-C

223344436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182617063-G-A

223344526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616963-G-T

223344876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616665-T-C

223344930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616611-G-A

223345040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616491-T-C

223345040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616491-T-G

223345103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616441-C-T

223345396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616159-T-C

223345408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616147-G-A

223345408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182616147-G-C

223345816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182615700-C-T

223345818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182615698-T-C

223345900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182615653-A-G

223345969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182615585-C-T

http://identifiers.org/hco/1/GRCh38#223346321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182615067-A-C

223346431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182614955-C-T

223346522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182614871-C-G

223346747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182614678-C-T

223347895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182612095-G-A

223348040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611975-C-T

223348159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611836-A-G

223348366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611632-T-C

223348381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611617-T-G

223348494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611516-A-G

223348692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611354-A-G

223348763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182611248-T-C

223349075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610966-C-T

223349108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610840-G-C

223349382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610428-T-C

223349382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610428-T-G

223349657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610154-G-A

223349763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610053-C-T

223349805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182610012-C-T

223350109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609696-T-C

http://identifiers.org/hco/1/GRCh38#223350197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182609612-A-C

223350290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609524-T-A

223350366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609447-G-A

223350369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609444-G-A

223350414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609405-C-T

223350415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609404-A-G

223350482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609356-G-A

223350520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182609317-C-T

223350772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608922-G-A

223351232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608508-C-T

http://identifiers.org/hco/1/GRCh38#223351339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182608432-A-C

223351836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608104-A-G

223351866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608074-C-G

223351894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608046-C-G

223351894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182608046-C-T

223352273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607707-C-G

223352490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607494-A-G

223352545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607445-C-T

223352665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607329-C-G

223352771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607260-G-A

223352822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182607121-C-T

223352917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182606941-G-C

223353081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182606805-T-A

223353341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182606495-C-T

223353376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182606461-G-A

223354226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182605048-A-G

223354921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182602336-T-C

223355676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182602162-T-C

223355750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182602083-C-T

http://identifiers.org/hco/1/GRCh38#223355782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182602051-C-A

223355782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182602051-C-G

223355913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601938-C-T

223355970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601898-G-A

223355999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601856-G-C

http://identifiers.org/hco/1/GRCh38#223356148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182601678-C-A

223356209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601619-A-T

223356529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601389-C-T

223356566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601356-G-A

223356964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601141-C-G

223357031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182601076-C-T

223357266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182600885-T-C

223357539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182600651-T-C

223357803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182600394-A-G

223357850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182600346-T-C

223358016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182600181-G-C

223358678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 182599168-G-T

http://identifiers.org/hco/1/GRCh38#223358807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182597187-C-A

223359033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182596969-G-A

223359135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182596915-A-G

http://identifiers.org/hco/1/GRCh38#223359207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182596849-C-A

223359325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182596745-A-G

http://identifiers.org/hco/1/GRCh38#223359673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182596457-C-A

223359773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182596383-T-A

223359866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182596288-A-G

223360165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182596008-G-C

223360221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182595966-T-C

http://identifiers.org/hco/1/GRCh38#223360252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182595935-C-A

http://identifiers.org/hco/1/GRCh38#223360312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182595879-C-A

http://identifiers.org/hco/1/GRCh38#223360342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182595850-C-A

223360342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595850-C-T

223360406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595787-T-C

223360415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595778-G-A

223360415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595778-G-T

223360870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595320-T-C

223360946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595241-G-A

223360978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182595202-G-C

223361182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594802-G-A

223361227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594766-T-A

223361239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594754-T-C

http://identifiers.org/hco/1/GRCh38#223361675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182594343-A-C

223361676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594342-G-C

223361694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594324-G-T

223361904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182594134-G-C

http://identifiers.org/hco/1/GRCh38#223362072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182593973-C-A

223362106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182593924-T-A

223362903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182593085-T-C

223362949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182593039-C-T

http://identifiers.org/hco/1/GRCh38#223363144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182592881-C-A

223363144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182592881-C-T

223363213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182592816-G-A

223363213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182592816-G-T

223363349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 182592680-G-A

223363652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 182592364-A-G

223363739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182592276-G-A

223363739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182592276-G-T

223363749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 182592266-A-G

http://identifiers.org/hco/1/GRCh38#223363985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182592032-C-A

223363985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182592032-C-T

http://identifiers.org/hco/1/GRCh38#223364000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#182592017-C-A

223364000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182592017-C-T

223364098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 182591918-C-T

223364146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 182591870-C-T

223364172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 182591803-G-A

223364172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 182591803-G-T

223364186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 182591791-G-A

223364339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron variant
orthologous variants: 182591646-G-A

223364339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron variant
orthologous variants: 182591646-G-T

223364673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron_variant, undefined
orthologous variants: 182591327-C-T

223364906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron variant
orthologous variants: 182591129-G-A

223364907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron variant
orthologous variants: 182591128-C-T

223365006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25470
most severe consequence: intron variant
orthologous variants: 182591058-C-G