74202770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58041867-G-A

74202770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58041867-G-T

74202806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58041783-G-A

74202806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58041783-G-T

http://identifiers.org/hco/15/GRCh38#74202822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041767-C-A

74202822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58041767-C-T

http://identifiers.org/hco/15/GRCh38#74202865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041718-C-A

74202865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58041718-C-T

74202901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58041682-C-T

74202988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58041662-A-G

http://identifiers.org/hco/15/GRCh38#74203001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041651-A-C

74203001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 58041651-A-G

74203001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 58041651-A-T

http://identifiers.org/hco/15/GRCh38#74203043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041609-C-A

74203043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58041609-C-G

74203043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58041609-C-T

http://identifiers.org/hco/15/GRCh38#74203294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041386-C-A

74203294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041386-C-T

74203362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041326-G-A

74203362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041326-G-T

http://identifiers.org/hco/15/GRCh38#74203430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58041261-C-A

74203430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041261-C-G

74203447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041244-A-G

74203558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58041157-T-C

74203700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040826-G-A

74203759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040774-A-T

74203835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040701-A-G

74203848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040688-G-A

74203928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040629-T-C

74203948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040609-G-C

74203974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040583-G-A

74204599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040017-G-C

74204602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58040014-A-G

74205896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58039463-C-T

74206015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58039357-G-A

74206033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58039339-T-C

74206211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58039130-G-A

74206373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038991-G-A

74206657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038727-G-A

74206715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038676-A-G

74206733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038654-A-G

74207174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038356-G-A

http://identifiers.org/hco/15/GRCh38#74207311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58038236-C-A

http://identifiers.org/hco/15/GRCh38#74207558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58038020-C-A

http://identifiers.org/hco/15/GRCh38#74207563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58038015-C-A

74207563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038015-C-G

74207563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58038015-C-T

http://identifiers.org/hco/15/GRCh38#74207568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58038011-C-A

74207597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037982-T-G

74207615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037966-G-A

74207615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037966-G-C

74207615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037966-G-T

74207672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037906-G-T

http://identifiers.org/hco/15/GRCh38#74207782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58037816-C-A

74207782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58037816-C-T

74207876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58037697-T-A

74207876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58037697-T-C

74208074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037549-G-A

74208074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037549-G-C

74208074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037549-G-T

74208087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037536-G-A

74208087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037536-G-T

http://identifiers.org/hco/15/GRCh38#74208149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58037481-C-A

74208149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037481-C-T

74208185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037447-G-T

74208190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037442-G-A

74208190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037442-G-T

74208218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037401-C-T

http://identifiers.org/hco/15/GRCh38#74208468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58037194-C-A

74208468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037194-C-G

74208579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037106-G-A

74208651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037031-T-A

74208651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58037031-T-C

http://identifiers.org/hco/15/GRCh38#74208948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58036799-C-A

74209305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036485-T-C

74209340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036451-T-A

74209394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 58036396-A-G

74209558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58036229-T-A

74209579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036208-T-G

74209609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036185-A-G

74209609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036185-A-T

74209613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58036181-T-A

http://identifiers.org/hco/15/GRCh38#74209641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#58036154-C-A

74209641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036154-C-T

74209642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58036153-A-G

http://identifiers.org/hco/15/GRCh38#74209724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58036086-C-A

http://identifiers.org/hco/15/GRCh38#74209725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58036085-C-A

74209725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58036085-C-T

74209740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58036070-G-A

74209740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58036070-G-C

74209740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58036070-G-T

74209957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58035870-T-A

74210561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034464-G-C

74210684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034324-G-A

74210684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034324-G-C

74210839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034174-A-G

http://identifiers.org/hco/15/GRCh38#74210910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58034104-C-A

74210910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034104-C-G

74210919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034095-T-C

74210952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58034062-A-G

74211145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58033875-A-G

74211739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58033650-G-A

http://identifiers.org/hco/15/GRCh38#74212079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58032193-C-A

74212079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58032193-C-T

74212080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58032192-T-C

74212080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58032192-T-G

74212145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 58032127-G-A

74212145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 58032127-G-C

74212145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 58032127-G-T

http://identifiers.org/hco/15/GRCh38#74212170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58032116-C-A

74212170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032116-C-T

74212174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032112-G-T

74212188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032092-T-C

74212217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032065-A-G

74212218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032064-G-A

74212245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 58032044-A-G

74212313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031972-T-C

74212317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031968-G-T

74212350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031936-G-T

http://identifiers.org/hco/15/GRCh38#74212370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58031917-C-A

74212373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031914-G-A

74212373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031914-G-T

http://identifiers.org/hco/15/GRCh38#74212409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58031881-C-A

74212409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031881-C-G

74212436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031855-G-A

74212525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58031792-G-A

74212525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58031792-G-T

http://identifiers.org/hco/15/GRCh38#74212564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58031765-C-A

74212564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58031765-C-T

74212596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58031735-A-G

74213734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031582-G-T

74213848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031496-G-A

74214073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031279-G-A

74214075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031277-G-A

74214100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031252-G-C

74214153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58031203-G-A

74214528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030910-C-T

74214571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030867-A-G

74214632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030815-T-C

74214776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030683-G-T

74215071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030201-A-G

74215148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58030153-C-T

74215356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58029935-G-A

74215434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58029852-G-A

74215434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58029852-G-T

74215945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58029031-A-G

74215956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58029020-G-A

74216001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58028975-G-A

74216112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58028859-G-A

74216176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58028800-C-T

74217059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026242-A-G

74217193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026107-A-G

74217193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58026107-A-T

74217266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58026031-G-C

74217266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58026031-G-T

http://identifiers.org/hco/15/GRCh38#74217551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58025746-A-C

74217617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025678-A-G

74217637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025658-G-A

http://identifiers.org/hco/15/GRCh38#74217699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58025597-C-A

74217749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025540-G-T

74217868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025434-C-G

http://identifiers.org/hco/15/GRCh38#74217911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58025398-C-A

74217911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025398-C-T

74217952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025368-C-T

74218200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025165-C-T

74218260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025122-G-C

74218365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025028-G-T

http://identifiers.org/hco/15/GRCh38#74218366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58025027-C-A

74218366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58025027-C-T

http://identifiers.org/hco/15/GRCh38#74218372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58025021-C-A

74218437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024972-T-C

74218453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024956-G-T

74218679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58024730-G-A

74218763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58024646-C-T

74218788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58024621-C-T

74218975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024517-G-A

74218975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024517-G-T

74219262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024404-C-T

74219621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024063-G-A

74219668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024026-G-T

74219689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58024004-C-T

74219713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58023978-C-G

74219953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58023733-C-G

74220611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58023143-G-A

http://identifiers.org/hco/15/GRCh38#74221245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58022327-A-C

74221245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58022327-A-T

http://identifiers.org/hco/15/GRCh38#74221287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58022290-A-C

74221287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022290-A-G

74221287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022290-A-T

74221293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022284-G-A

74221293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022284-G-T

74221295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022282-A-G

74221301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022276-A-G

74221321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022260-G-T

74221422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022200-G-A

74221422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022200-G-T

74221436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022186-G-A

74221436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58022186-G-C

74221648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58022079-G-A

74221648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58022079-G-T

74222343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021507-C-T

74222709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021146-G-A

74222709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021146-G-T

74222730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021119-C-T

http://identifiers.org/hco/15/GRCh38#74222760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58021081-C-A

74222761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021080-C-T

74222819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021015-T-C

74222819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58021015-T-G

http://identifiers.org/hco/15/GRCh38#74223711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58020168-C-A

74223942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58019932-G-A

74224615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58019335-G-C

74224642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58019307-G-A

74225153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58018776-T-A

74225158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58018691-C-G

74225158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58018691-C-T

74225283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018575-C-T

74225450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018542-G-A

74225450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018542-G-C

74225450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018542-G-T

74225598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018435-A-G

http://identifiers.org/hco/15/GRCh38#74225608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58018424-A-C

74225608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018424-A-G

74225707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58018342-A-G

74226194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017991-G-A

http://identifiers.org/hco/15/GRCh38#74226256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58017950-A-C

74226484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017728-C-T

74226982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017570-G-A

74227039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017525-T-G

74227147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017407-C-T

74227292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017266-C-T

74227317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017241-C-T

74227368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58017207-C-T

74227618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58016934-A-G

74227893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58016670-C-T

74227906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58016655-C-G

http://identifiers.org/hco/15/GRCh38#74228603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58015234-C-A

74228642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58015190-G-C

74228664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58015160-G-A

74228664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58015160-G-T

74228706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58015126-C-T

74228757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58015071-G-A

74228875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58014953-G-C

74228900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58014927-G-A

74229386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58014310-G-A

74229386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58014310-G-C

74229735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58014003-G-A

74230133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013653-G-A

74230259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013573-G-A

74230259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013573-G-T

http://identifiers.org/hco/15/GRCh38#74230299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58013541-C-A

http://identifiers.org/hco/15/GRCh38#74230300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58013540-A-C

74230448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013394-A-T

74230517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013325-G-C

74230645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013218-G-A

http://identifiers.org/hco/15/GRCh38#74230650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58013213-C-A

74230785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58013100-C-T

74230980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58012906-A-T

74231197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58012717-C-T

74231292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58012637-A-G

74231292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58012637-A-T

74231462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58012499-G-T

74236144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009736-G-A

74236144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009736-G-T

http://identifiers.org/hco/15/GRCh38#74236146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009734-A-C

74236146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009734-A-T

http://identifiers.org/hco/15/GRCh38#74236178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009707-A-C

74236178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009707-A-G

74236293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009611-T-C

74236321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009583-A-G

74236321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009583-A-T

74236398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009514-T-C

74236398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009514-T-G

http://identifiers.org/hco/15/GRCh38#74236519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009398-C-A

74236519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009398-C-T

http://identifiers.org/hco/15/GRCh38#74236533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009388-C-A

74236533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009388-C-G

74236533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009388-C-T

http://identifiers.org/hco/15/GRCh38#74236560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009362-C-A

74236560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009362-C-T

http://identifiers.org/hco/15/GRCh38#74236561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009361-C-A

74236561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009361-C-T

http://identifiers.org/hco/15/GRCh38#74236597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58009343-C-A

74236643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009299-T-A

74236643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009299-T-C

74236648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009294-G-A

74236648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58009294-G-T

74236869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009152-T-C

74236870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009151-G-T

74236949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58009095-T-G

74237120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58008992-T-C

74239971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58008130-G-A

74240070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58008056-G-C

74240070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58008056-G-T

74240192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58007936-C-T

74240407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007744-G-A

74240519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007620-A-G

74240531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007608-G-A

74240556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007583-G-A

74240573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007572-G-T

74240978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007494-G-A

74240978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007494-G-C

74240978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007494-G-T

74241175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007311-C-T

74241446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58007051-G-A

74243337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58006809-A-G

74243343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58006803-G-A

74243551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58006569-G-A

74243988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58005956-A-G

74244035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58005909-T-G

74244238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005635-G-T

74244610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005134-A-G

74244719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58005042-C-T

74245173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004685-C-T

74245313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004536-G-A

74245314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004535-G-T

74245397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004441-C-T

74245441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004397-C-G

74245441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004397-C-T

74245470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004361-G-A

74245470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004361-G-C

74245487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004344-C-T

74245836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58004030-A-G

74245979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58003892-G-C

http://identifiers.org/hco/15/GRCh38#74246072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58003785-C-A

74246122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58003717-C-T

74248193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58002067-A-G

74248235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58002036-T-C

74248284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001997-G-T

74248429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001885-C-G

http://identifiers.org/hco/15/GRCh38#74249963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58001408-C-A

74249998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001386-T-C

74250066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001326-C-T

74250068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001324-C-T

74250107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001286-T-C

74250372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58001041-C-T

http://identifiers.org/hco/15/GRCh38#74250403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#58001011-A-C

74250675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000795-G-A

74250675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000795-G-T

74250681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000789-C-T

74250916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000542-T-C

74251074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000395-G-C

74251146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000323-G-C

74251515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58000014-C-T

74251599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57999943-G-A

74251716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57999852-C-T

http://identifiers.org/hco/15/GRCh38#74252108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57999652-A-C

74252551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57999403-G-A

74252551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57999403-G-C

74252551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57999403-G-T

74252938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57999055-T-C

74257218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57998091-C-T

74257378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57997771-G-A

74257433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57997713-T-G

74257434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57997712-T-C

74258167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57997053-C-T

74258548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996570-G-A

74258634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996425-A-G

74258713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996301-A-T

74258763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996247-C-T

74258901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996102-C-T

74258949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57996052-T-C

74259190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995833-G-A

74259190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995833-G-C

74259212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995811-G-A

74259212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995811-G-C

74259923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57995109-G-T

74260108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994919-G-A

74261717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994608-G-A

74261781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994542-A-G

http://identifiers.org/hco/15/GRCh38#74261895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57994459-C-A

74261922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994432-G-A

74262043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994313-G-A

74262261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57994114-C-T

http://identifiers.org/hco/15/GRCh38#74262394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57993992-A-C

74262434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57993963-C-T

74262462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57993935-A-G

74262516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57993881-C-G

74262581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57993814-G-T

http://identifiers.org/hco/15/GRCh38#74262595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57993803-C-A

74262595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993803-C-T

http://identifiers.org/hco/15/GRCh38#74262605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57993793-C-A

74262605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993793-C-T

http://identifiers.org/hco/15/GRCh38#74262622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57993771-C-A

http://identifiers.org/hco/15/GRCh38#74262647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57993747-A-C

74262944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993449-T-A

74263285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993160-G-T

74263453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993106-T-G

74263553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57993001-A-G

74263895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992751-G-C

74264035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992662-C-G

74264035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992662-C-T

74264247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992457-A-G

74264349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992354-G-A

74264388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992312-G-A

74264402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992298-T-C

74264415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992285-T-C

74264421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992279-C-T

74264580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992169-G-A

74264588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992162-G-A

74264656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992082-T-C

74264679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992059-A-G

74264715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57992023-A-G

74264884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991859-A-T

74264906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991842-A-G

74265035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57991717-G-A

74265065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57991679-G-C

74265338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57991530-T-C

74265539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991338-C-T

74265627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57991261-G-A

74266020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990867-T-C

74266097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990699-G-A

74266356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990411-G-A

74266498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57990307-A-G

http://identifiers.org/hco/15/GRCh38#74266561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57989439-A-C

74266561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989439-A-G

74266561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989439-A-T

74266563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989437-T-A

74266563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989437-T-C

74266563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989437-T-G

http://identifiers.org/hco/15/GRCh38#74266576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57989424-C-A

74266576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989424-C-G

74266576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57989424-C-T

74266706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57989322-A-G

http://identifiers.org/hco/15/GRCh38#74266729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57989299-A-C

74267507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988974-G-A

74267507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988974-G-T

74267669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988813-T-C

74267835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988642-G-T

74268062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988446-T-G

74268082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988426-G-A

74268219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988289-T-A

74268219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988289-T-C

74268219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988289-T-G

74268337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57988179-T-C

74268387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57988129-T-A

74268387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57988129-T-C

74268387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57988129-T-G

74268467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988049-G-A

74268467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988049-G-T

74268554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57988002-A-G

74268567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987989-G-A

74268567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987989-G-C

74268567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987989-G-T

74268581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987962-A-G

74268581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987962-A-T

74268601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987942-G-A

74268601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987942-G-T

http://identifiers.org/hco/15/GRCh38#74268687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57987641-C-A

74268687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987641-C-T

74268702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987620-A-T

74268886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987452-C-T

74269162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987217-C-T

74269296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987115-C-T

74269318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57987112-T-C

74269584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57986940-C-T

74269709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57986850-G-A

74269709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57986850-G-C

74270173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57986443-G-A

74271479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985162-G-A

74271479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985162-G-C

74271581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985058-A-G

http://identifiers.org/hco/15/GRCh38#74271592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57985043-C-A

74271592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57985043-C-T

74271627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984987-G-T

74271631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984973-G-A

74271631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984973-G-T

74271821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984810-T-G

http://identifiers.org/hco/15/GRCh38#74271884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57984780-C-A

74271887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984777-G-A

74271887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984777-G-T

74271928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984745-T-C

74271942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984726-G-C

74271942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984726-G-T

74272016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984655-C-T

74272050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984626-C-G

74272077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984608-A-G

74272681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984027-G-A

74272692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984016-G-T

http://identifiers.org/hco/15/GRCh38#74272708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57984000-C-A

74272708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984000-C-G

74272708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57984000-C-T

http://identifiers.org/hco/15/GRCh38#74272955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57983783-C-A

http://identifiers.org/hco/15/GRCh38#74273002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57983738-C-A

74273002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57983738-C-T

http://identifiers.org/hco/15/GRCh38#74273026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57983715-C-A

74273026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57983715-C-G

74273026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57983715-C-T

74273125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57983650-T-A

74273304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57983473-A-G

74273972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982791-C-T

74273975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982788-G-T

74274119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982569-T-C

74274137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982552-T-C

74274328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982368-A-G

74274362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982336-G-A

74274417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57982295-T-C

74274923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57981826-G-A

74275119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57981662-A-G

74275342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57981432-C-G

74275492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57981320-T-A

74276015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57981145-A-G

74276162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980982-C-T

74276239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980896-G-C

74277014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980257-G-A

74277027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57980244-G-A

74277688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979470-C-T

74277795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979359-C-T

74277931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979208-G-A

74278060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979067-A-G

74278086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57979041-T-C

74278213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57978905-C-T

74278216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57978902-G-C

74278240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57978874-C-G

74278591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57978567-T-A

74278631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57978532-A-G

http://identifiers.org/hco/15/GRCh38#74279908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57977294-C-A

74279908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977294-C-T

74279976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57977234-G-A

74280074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57977136-T-C

74280074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57977136-T-G

74280142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977075-G-A

74280142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977075-G-T

74280169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977049-C-T

74280193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977025-G-A

74280193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977025-G-C

74280207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977008-G-A

74280207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977008-G-T

74280215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977000-G-A

74280215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57977000-G-T

74280393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976871-G-T

74280510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976744-C-T

74280579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976633-G-A

74280579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976633-G-T

http://identifiers.org/hco/15/GRCh38#74280586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57976626-A-C

74280586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976626-A-G

74280594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976618-T-C

74280594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976618-T-G

74280595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976617-G-A

74280595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976617-G-T

74280615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976598-T-G

74280712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57976459-T-C

74280727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57976444-A-G

74280740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57976431-A-G

74280740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57976431-A-T

74280799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57976372-A-G

74280844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976327-G-A

74280844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976327-G-T

74280855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976311-G-A

74280855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976311-G-C

74280855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976311-G-T

74280897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976128-T-C

http://identifiers.org/hco/15/GRCh38#74280906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57976120-C-A

74280906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976120-C-G

74280906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976120-C-T

74281055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57976001-G-A

74281461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57975147-T-C

http://identifiers.org/hco/15/GRCh38#74281664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57974964-C-A

74281664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974964-C-T

74281707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974929-G-A

74281707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974929-G-C

74281707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974929-G-T

http://identifiers.org/hco/15/GRCh38#74281744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57974884-C-A

74281793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57974840-A-G

74281851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 57974782-T-C

74281851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 57974782-T-G

74282120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974497-C-T

74282331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974305-T-C

74282348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974288-C-G

74282627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57974052-C-T

74282697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57973984-G-T

74283289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57973167-G-A

74283289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57973167-G-T

74283443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57973034-A-G

74283831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972646-A-G

http://identifiers.org/hco/15/GRCh38#74283834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57972643-C-A

74283834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972643-C-T

74283863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972612-A-G

74284101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972390-C-T

74284137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972351-T-A

74284279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972211-G-C

74284454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972039-C-G

74284454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57972039-C-T

http://identifiers.org/hco/15/GRCh38#74284492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57972011-C-A

74284893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971640-G-T

http://identifiers.org/hco/15/GRCh38#74284921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57971612-C-A

74284921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971612-C-G

74284952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971589-A-G

74284953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971588-T-C

74285254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971363-A-G

74285452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971177-T-A

74285567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57971069-C-T

74286318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57970664-C-T

74286382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57970600-C-G

http://identifiers.org/hco/15/GRCh38#74286574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57970413-A-C

74288959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57970225-A-G

74289086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57970105-G-C

74289112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57970079-C-T

74289872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969473-G-A

74289935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969415-C-T

74290082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969259-A-G

74290146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969204-T-C

74290204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969169-G-A

74290204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969169-G-C

74290247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57969126-G-A

74292203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57967862-G-A

74293082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57967566-T-G

74294993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57966280-G-A

74294993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57966280-G-T

74295543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965845-G-A

74295576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965816-G-A

74295717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965707-G-A

http://identifiers.org/hco/15/GRCh38#74295740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57965685-C-A

74295740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965685-C-T

74295893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57965559-C-T

74295965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965505-A-G

74296024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57965450-A-G

http://identifiers.org/hco/15/GRCh38#74296072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57965408-C-A

74296072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965408-C-G

74296072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965408-C-T

74296090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965391-T-C

74296325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57965204-T-C

74296966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57964914-G-A

74296971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57964909-C-T

74297072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57964815-A-G

74297176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57964719-G-A

74297716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57964483-A-G

74297918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57964317-G-A

74298284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57964005-G-T

74298355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963944-A-G

http://identifiers.org/hco/15/GRCh38#74299670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57963615-C-A

http://identifiers.org/hco/15/GRCh38#74299728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57963576-C-A

74299728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963576-C-G

http://identifiers.org/hco/15/GRCh38#74299771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57963526-C-A

74299771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963526-C-T

74299812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963492-A-G

74299844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963454-T-A

74299844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963454-T-C

http://identifiers.org/hco/15/GRCh38#74299979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57963388-C-A

74299979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963388-C-T

http://identifiers.org/hco/15/GRCh38#74299984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57963383-C-A

74300070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963298-G-A

74300070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963298-G-T

74300099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57963269-A-G

74300455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962952-T-C

74300514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962900-A-G

http://identifiers.org/hco/15/GRCh38#74300548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57962863-C-A

74300548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962863-C-T

74300595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962807-T-C

74300604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962798-T-C

74300689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57962707-T-C

74300722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57962674-G-A

74300722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57962674-G-T

http://identifiers.org/hco/15/GRCh38#74300811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57962605-C-A

74300811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57962605-C-T

http://identifiers.org/hco/15/GRCh38#74300813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57962603-C-A

74300813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57962603-C-T

http://identifiers.org/hco/15/GRCh38#74300830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57962601-C-A

74300830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962601-C-T

74301135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962366-G-A

74301135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962366-G-T

http://identifiers.org/hco/15/GRCh38#74301142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57962359-C-A

74301236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962271-G-A

74301236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962271-G-C

74301236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962271-G-T

74301346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962215-A-G

74301534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962057-A-G

74301536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962055-G-A

74301569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57962025-G-T

74301669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961984-G-A

74301669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961984-G-T

74301690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961963-G-T

http://identifiers.org/hco/15/GRCh38#74301882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57961597-C-A

74301909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961570-G-A

74301909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961570-G-C

74301909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961570-G-T

74301963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961515-A-T

74302044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961435-A-G

74302229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961263-T-C

74302229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961263-T-G

74302297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961196-T-G

74302334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961170-T-C

74302396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961108-G-T

http://identifiers.org/hco/15/GRCh38#74302401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57961103-C-A

74302401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961103-C-G

74302403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57961101-T-C

74302519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960984-A-G

74302577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960927-G-T

74302600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960904-G-A

74302600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960904-G-T

74302687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960892-T-C

74302719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960863-G-A

74302719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960863-G-T

http://identifiers.org/hco/15/GRCh38#74302802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57960781-C-A

74302802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960781-C-T

74302875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960720-G-T

74302936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960659-T-C

74302981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960623-T-C

http://identifiers.org/hco/15/GRCh38#74303013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57960593-C-A

74303013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57960593-C-T

http://identifiers.org/hco/15/GRCh38#74303074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57960558-C-A

http://identifiers.org/hco/15/GRCh38#74303136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57960496-C-A

74303136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960496-C-T

http://identifiers.org/hco/15/GRCh38#74303494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57960303-C-A

74303494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960303-C-G

74303494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960303-C-T

74303693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960110-G-A

74303693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960110-G-T

74303777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960049-G-A

74303777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960049-G-T

74303825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960016-A-G

74303836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57960005-G-T

74303850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959993-G-T

74303957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959830-G-T

74303977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959796-G-A

74303977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959796-G-C

74303977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959796-G-T

http://identifiers.org/hco/15/GRCh38#74304026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57959575-C-A

74304074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57959523-C-T

http://identifiers.org/hco/15/GRCh38#74304150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57959452-C-A

74304150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57959452-C-G

74304375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959278-G-A

74304375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959278-G-T

74304610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959035-G-A

74304610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959035-G-T

http://identifiers.org/hco/15/GRCh38#74304619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57959026-C-A

74304619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959026-C-T

74304671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57959007-T-C

74304738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958943-G-A

74304774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958902-G-A

74304779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958895-G-A

74304873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958823-C-T

74305606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958486-G-A

74305782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958377-T-C

74305792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958367-G-A

74305936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958248-C-T

74306005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958181-G-A

74306026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958168-G-A

74306206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57958010-A-G

74306271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957948-C-T

74306280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957939-T-C

74307123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957455-G-A

74307183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957398-G-A

74307202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957379-G-A

74307346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57957258-T-C

74307848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956827-A-G

74307849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956826-C-T

74307930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956740-T-C

74308337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956373-G-C

74308493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956217-C-G

74308493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57956217-C-T

74308917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955875-G-A

74308943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955853-A-G

74309120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955723-A-G

74309466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955531-C-T

74309469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955528-C-T

74309635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57955397-G-A

74310845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57954220-T-G

74311006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57954059-G-A

74311247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57953382-C-G

74311268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57953361-T-G

74311295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57953334-C-G

74311299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57953330-T-C

http://identifiers.org/hco/15/GRCh38#74311464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57953163-C-A

74311492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57953147-A-G

74312179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57952656-T-G

74312241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57952594-C-T

74312938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57951941-A-G

74316120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57951256-T-G

74316168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57951207-T-G

74316546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57950796-C-T

74316838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57950532-A-T

74317477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57950261-G-A

74317477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57950261-G-C

74318031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949778-G-A

http://identifiers.org/hco/15/GRCh38#74318096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949716-A-C

74318096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949716-A-G

http://identifiers.org/hco/15/GRCh38#74318111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949707-A-C

74318111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949707-A-G

http://identifiers.org/hco/15/GRCh38#74318131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949700-A-C

74318217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949653-G-A

74318240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949630-G-C

74318406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949489-G-T

http://identifiers.org/hco/15/GRCh38#74318434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949468-C-A

74318434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949468-C-T

http://identifiers.org/hco/15/GRCh38#74318435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949467-C-A

http://identifiers.org/hco/15/GRCh38#74318441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949461-A-C

74318441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949461-A-G

http://identifiers.org/hco/15/GRCh38#74318449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949453-C-A

74318449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949453-C-G

74318449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949453-C-T

http://identifiers.org/hco/15/GRCh38#74318453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949449-C-A

74318453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57949449-C-G

74318548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949355-C-T

74318554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949349-G-A

74318554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949349-G-C

74318554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949349-G-T

74318563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949340-T-C

74318596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949307-G-A

http://identifiers.org/hco/15/GRCh38#74318630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949273-C-A

74318630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949273-C-G

http://identifiers.org/hco/15/GRCh38#74318650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949253-A-C

74318650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57949253-A-G

http://identifiers.org/hco/15/GRCh38#74318669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949233-C-A

74318669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949233-C-T

74318684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949218-T-C

74318727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949176-G-A

74318757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949146-C-G

74318757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949146-C-T

http://identifiers.org/hco/15/GRCh38#74318764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949139-C-A

74318764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949139-C-T

http://identifiers.org/hco/15/GRCh38#74318765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949137-C-A

http://identifiers.org/hco/15/GRCh38#74318818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57949084-C-A

74318818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57949084-C-T

74319444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948857-A-G

74319444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948857-A-T

74319454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948847-G-A

74319454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948847-G-T

74319456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948845-G-T

http://identifiers.org/hco/15/GRCh38#74319490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57948814-C-A

74319580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57948716-A-G

74319678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57948626-T-C

74319700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948603-A-G

http://identifiers.org/hco/15/GRCh38#74319726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57948573-C-A

http://identifiers.org/hco/15/GRCh38#74319788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#57948503-C-A

74320005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948300-C-G

74320099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948204-G-A

74320099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948204-G-C

74320215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948057-G-C

74320252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57948014-T-C

74322421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57946285-T-C

74322633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57946124-A-T

74322831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57945905-C-T

74325541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57945196-T-C

74325612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57945102-T-C

74325668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57945055-A-G

74326897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57944411-G-A

http://identifiers.org/hco/15/GRCh38#74326921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57944393-C-A

74327175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57944164-A-G

74327287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57944032-T-C

74327672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943952-C-G

74327798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943852-A-G

74327800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943850-G-T

74327850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943795-G-T

http://identifiers.org/hco/15/GRCh38#74327954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57943697-C-A

74327958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943693-A-G

74328669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57943046-C-T

http://identifiers.org/hco/15/GRCh38#74328670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57943045-A-C

http://identifiers.org/hco/15/GRCh38#74328915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57942799-C-A

74328915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57942799-C-G

74328915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57942799-C-T

74329449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941693-A-T

74329492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941649-A-G

74329543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941599-T-C

74329807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941353-G-T

74329942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941228-G-A

74330119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941068-T-C

74330119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941068-T-G

74330120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941067-G-A

74330120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941067-G-T

74330141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941043-G-T

http://identifiers.org/hco/15/GRCh38#74330149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57941034-A-C

74330149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941034-A-G

74330179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57941005-G-T

74330255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940930-G-A

74330328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940855-G-A

74330328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940855-G-T

http://identifiers.org/hco/15/GRCh38#74330465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940755-C-A

74330465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940755-C-G

74330465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940755-C-T

http://identifiers.org/hco/15/GRCh38#74330481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940747-C-A

74330542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940669-G-C

74330542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940669-G-T

74330545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940666-A-G

http://identifiers.org/hco/15/GRCh38#74330558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940658-C-A

74330558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940658-C-T

http://identifiers.org/hco/15/GRCh38#74330565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940651-C-A

http://identifiers.org/hco/15/GRCh38#74330573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940643-C-A

74330573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940643-C-G

74330593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940628-G-A

74330593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940628-G-C

http://identifiers.org/hco/15/GRCh38#74330632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940619-C-A

http://identifiers.org/hco/15/GRCh38#74330675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940577-A-C

74330676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940576-G-T

74330689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940563-A-T

74330698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940554-G-A

74330788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940465-T-C

74330792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940461-G-A

74330792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940461-G-T

http://identifiers.org/hco/15/GRCh38#74330917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940364-C-A

74330917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940364-C-T

http://identifiers.org/hco/15/GRCh38#74330926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57940355-A-C

74330926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940355-A-G

74330928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940353-G-A

74330928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940353-G-T

74330947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940335-A-T

74331062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57940196-A-G

74331117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57940141-G-A

http://identifiers.org/hco/15/GRCh38#74331344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57939905-C-A

74331344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939905-C-T

74331350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939904-G-A

74331350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939904-G-T

http://identifiers.org/hco/15/GRCh38#74331354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57939900-C-A

74331354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939900-C-T

http://identifiers.org/hco/15/GRCh38#74331357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57939897-C-A

74331357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939897-C-T

74331382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939875-G-T

74331387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939870-C-T

74331442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939812-T-C

http://identifiers.org/hco/15/GRCh38#74331447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57939807-C-A

74331491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939761-G-A

74331732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939538-T-A

74331732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939538-T-C

http://identifiers.org/hco/15/GRCh38#74332555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57939119-C-A

74332555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57939119-C-T

http://identifiers.org/hco/15/GRCh38#74332871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57938861-C-A

74332871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57938861-C-T

http://identifiers.org/hco/15/GRCh38#74333129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57938629-C-A

74333129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57938629-C-G

74333129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57938629-C-T

http://identifiers.org/hco/15/GRCh38#74333141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57938616-C-A

74333141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57938616-C-T

74333208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57938558-T-C

74333235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57938529-G-A

74333235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57938529-G-T

74333251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57938513-G-A

74333251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57938513-G-T

http://identifiers.org/hco/15/GRCh38#74333284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57938480-C-A

74333284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57938480-C-T

http://identifiers.org/hco/15/GRCh38#74333612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57938081-C-A

74333612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57938081-C-T

74333700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937880-C-T

http://identifiers.org/hco/15/GRCh38#74333729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57937851-A-C

74333729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937851-A-G

http://identifiers.org/hco/15/GRCh38#74333741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57937839-C-A

74333741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937839-C-T

74333766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937814-G-A

http://identifiers.org/hco/15/GRCh38#74333780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57937799-C-A

74334804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937379-G-A

http://identifiers.org/hco/15/GRCh38#74334891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57937329-C-A

74334891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937329-C-G

74334891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57937329-C-T

http://identifiers.org/hco/15/GRCh38#74335179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57937041-C-A

74335179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57937041-C-G

74335179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57937041-C-T

74335245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936973-A-G

http://identifiers.org/hco/15/GRCh38#74335272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936942-A-C

74335272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936942-A-G

74335285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936929-G-A

74335285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936929-G-T

74335345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936872-G-A

74335402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936813-T-C

74335402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936813-T-G

http://identifiers.org/hco/15/GRCh38#74335513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936555-C-A

74335513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 57936555-C-T

74335553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936517-A-G

http://identifiers.org/hco/15/GRCh38#74335623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936436-C-A

74335623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936436-C-G

74335632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936427-G-A

74335632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 57936427-G-T

74335695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936373-G-A

74335695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936373-G-T

http://identifiers.org/hco/15/GRCh38#74335700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936369-C-A

74335702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936367-G-A

74335702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936367-G-T

http://identifiers.org/hco/15/GRCh38#74335706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936363-A-C

74335859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936213-A-G

74335893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936195-G-A

74335948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57936144-C-T

74336018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 57936074-C-T

74336023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 57936069-G-A

http://identifiers.org/hco/15/GRCh38#74336055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57936037-C-A

74336055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936037-C-T

74336056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936036-C-G

74336085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936008-G-A

74336085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57936008-G-T

74336111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57935987-A-G

74336125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57935973-A-T

http://identifiers.org/hco/15/GRCh38#74336180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57935754-C-A

74336429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense variant
orthologous variants: 57935548-A-T

http://identifiers.org/hco/15/GRCh38#74336440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26552
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#57935537-A-C