http://identifiers.org/hco/10/GRCh38#132186964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138665960-C-A

132186964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5 prime UTR variant
orthologous variants: 138665960-C-G

132186964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5 prime UTR variant
orthologous variants: 138665960-C-T

http://identifiers.org/hco/10/GRCh38#132187011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138665976-C-A

132187011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138665976-C-G

132187011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138665976-C-T

http://identifiers.org/hco/10/GRCh38#132187012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138665977-C-A

132187012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138665977-C-G

132187012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138665977-C-T

132187231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666208-G-A

132187231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666208-G-T

132187274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666251-C-T

132187440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666358-C-T

132187505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666467-G-A

132187507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666469-C-T

http://identifiers.org/hco/10/GRCh38#132187757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138666725-C-A

132187787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666746-C-G

132187865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666837-G-T

http://identifiers.org/hco/10/GRCh38#132187877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138666849-A-C

http://identifiers.org/hco/10/GRCh38#132188046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138666990-C-A

132188055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138666999-G-C

132188128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667080-C-T

132188170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667114-C-G

132188409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667328-G-A

132188471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667378-G-A

132188498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667391-C-T

132188642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667533-C-G

132188685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667575-G-C

132188714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667587-C-T

132188772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667640-G-A

132188962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667803-A-G

http://identifiers.org/hco/10/GRCh38#132188983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138667824-A-C

132189040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138667871-A-G

http://identifiers.org/hco/10/GRCh38#132189302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138668117-C-A

132189302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668117-C-T

132189303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668118-C-T

132189311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668122-C-G

132189311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668122-C-T

132189340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668151-C-T

132189394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668206-C-T

132189498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668299-C-T

132189561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668360-C-G

http://identifiers.org/hco/10/GRCh38#132189616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138668392-A-C

132189620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668399-C-G

132189620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668399-C-T

132189625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138668404-G-A

http://identifiers.org/hco/10/GRCh38#132189964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138668724-C-A

132190369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669079-G-C

132190466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669156-G-A

132190569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669264-T-C

132190631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669324-A-G

132190631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669324-A-T

http://identifiers.org/hco/10/GRCh38#132190647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138669341-C-A

132190647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669341-C-T

132190652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669346-A-G

http://identifiers.org/hco/10/GRCh38#132190685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138669381-C-A

132190685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669381-C-T

132190686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669382-A-G

132190686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669382-A-T

132190773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138669452-G-A

http://identifiers.org/hco/10/GRCh38#132192261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138669719-C-A

132192261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669719-C-T

http://identifiers.org/hco/10/GRCh38#132192351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138669792-C-A

132192356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 138669797-T-C

132192406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669835-A-G

132192414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669843-G-A

132192414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669843-G-T

132192447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669876-T-C

132192458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669889-G-A

132192458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 138669889-G-T

132192526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669941-T-C

132192526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669941-T-G

132192531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138669946-G-A

132192586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670004-C-T

132192633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670044-C-G

132192766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138670183-T-C

132192817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138670234-G-A

132192890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670331-G-A

http://identifiers.org/hco/10/GRCh38#132192891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138670332-C-A

132192891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670332-C-G

132192891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670332-C-T

132193129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670617-T-C

132193160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670647-G-A

132193254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670706-G-A

132193633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670852-T-G

132193667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670869-C-T

132193718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138670885-G-T

132193956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671053-G-A

132194005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671108-C-T

132194036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671118-G-A

132194150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671218-A-G

132194255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671292-C-T

132194298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138671335-A-T

132194545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138671523-C-T

132194758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671693-G-A

132194758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671693-G-T

132194782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671717-G-A

http://identifiers.org/hco/10/GRCh38#132194864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138671797-C-A

132194864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138671797-C-T

132194918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138671851-C-T

132194921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138671854-G-A

132194921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138671854-G-T

132195028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671959-G-A

132195028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671959-G-T

132195030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671961-T-C

132195030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138671961-T-G

132195080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672025-T-C

132195138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672079-G-A

132195138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672079-G-C

132195138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672079-G-T

132195139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672080-A-G

132195188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672128-A-T

132195425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672375-A-G

132195691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672607-C-T

132195758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672675-C-T

132195839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672694-G-A

132195900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672722-G-A

132195900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672722-G-C

132196163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672864-G-A

132196172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672873-T-C

132196193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672877-C-G

132196289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138672971-C-T

132196355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138673045-C-T

http://identifiers.org/hco/10/GRCh38#132196411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138673112-C-A

132196716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138673418-G-A

132196716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138673418-G-T

132196725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138673429-G-A

132196725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138673429-G-T

132196959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673621-A-G

132196960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673622-T-C

132196997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673654-G-A

http://identifiers.org/hco/10/GRCh38#132197083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138673739-C-A

132197083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138673739-C-T

132197142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673807-T-C

132197163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673827-T-A

132197163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673827-T-C

132197197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673875-A-G

132197245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138673913-T-C

132198288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674189-G-T

132198343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674246-G-T

http://identifiers.org/hco/10/GRCh38#132198351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674254-C-A

http://identifiers.org/hco/10/GRCh38#132198379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674280-A-C

http://identifiers.org/hco/10/GRCh38#132198395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674295-C-A

132198396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674296-A-G

http://identifiers.org/hco/10/GRCh38#132198399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674299-C-A

132198399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674299-C-T

http://identifiers.org/hco/10/GRCh38#132198512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674394-C-A

132198512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674394-C-G

132198512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674394-C-T

132198530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674417-A-T

http://identifiers.org/hco/10/GRCh38#132198593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674474-C-A

132198593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674474-C-G

132198593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674474-C-T

http://identifiers.org/hco/10/GRCh38#132198621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674510-C-A

132198621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674510-C-G

132198621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674510-C-T

132198669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674554-T-C

http://identifiers.org/hco/10/GRCh38#132198814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674740-C-A

132198914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense variant
orthologous variants: 138674836-G-A

http://identifiers.org/hco/10/GRCh38#132198946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674868-C-A

132198946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138674868-C-T

http://identifiers.org/hco/10/GRCh38#132199029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674979-C-A

132199029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674979-C-T

http://identifiers.org/hco/10/GRCh38#132199033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138674983-C-A

132199033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674983-C-G

132199036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674986-G-A

132199043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138674993-T-C

132199319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675250-T-C

132199338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675286-C-T

132199542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675473-C-G

132199851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675688-C-G

http://identifiers.org/hco/10/GRCh38#132199916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138675710-C-A

132199916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675710-C-T

132199923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675717-C-T

132199941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675735-C-T

132200149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675912-C-T

132200150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138675913-A-G

http://identifiers.org/hco/10/GRCh38#132200287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138676012-C-A

132200287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676012-C-T

132200313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676043-G-A

132200372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138676100-G-A

132200393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138676121-G-A

132200405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138676133-T-C

132200426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense variant
orthologous variants: 138676154-C-G

132200447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138676175-C-T

132200601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676324-G-A

132200601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676324-G-T

http://identifiers.org/hco/10/GRCh38#132200619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138676342-C-A

132200619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676342-C-G

132200619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676342-C-T

http://identifiers.org/hco/10/GRCh38#132200714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138676444-C-A

132200714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676444-C-T

132200716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676446-C-T

132200829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676570-G-A

132200829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676570-G-C

132200929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138676670-C-T

132201009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676747-G-A

132201054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138676783-A-G

132201917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138677710-G-A

132201963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: synonymous variant
orthologous variants: 138677755-C-T

132202209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138677996-G-A

132202209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138677996-G-T

http://identifiers.org/hco/10/GRCh38#132202237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138678024-C-A

http://identifiers.org/hco/10/GRCh38#132202261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138678051-C-A

132202261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678051-C-T

132202270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678060-C-T

132202369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678142-C-T

132202502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678273-A-G

http://identifiers.org/hco/10/GRCh38#132202537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138678305-C-A

132202537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678305-C-T

132202619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678361-A-T

http://identifiers.org/hco/10/GRCh38#132202702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138678442-C-A

132202702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 138678442-C-T

132202756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 138678496-G-T

132202768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, missense_variant
orthologous variants: 138678508-C-G

132202768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 138678508-C-T

132202783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 138678523-A-T

132202867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678612-G-A

http://identifiers.org/hco/10/GRCh38#132202884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138678625-C-A

132202884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678625-C-T

132202888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678633-G-A

132202888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678633-G-C

132202888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron variant
orthologous variants: 138678633-G-T

http://identifiers.org/hco/10/GRCh38#132203776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138679670-C-A

132203776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138679670-C-T

132203794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138679688-G-A

132203794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138679688-G-C

132203839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138679733-G-A

132203842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138679736-T-C

http://identifiers.org/hco/10/GRCh38#132203945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138679838-C-A

http://identifiers.org/hco/10/GRCh38#132204000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138679869-C-A

http://identifiers.org/hco/10/GRCh38#132204034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138679911-C-A

132204131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680037-C-T

132204394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680391-C-T

132204581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680552-G-A

132204590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680561-A-G

132204615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680581-C-T

132204739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680727-T-C

132204740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680728-G-A

132204740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680728-G-C

132204740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680728-G-T

http://identifiers.org/hco/10/GRCh38#132204792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138680768-C-A

132204792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138680768-C-T

http://identifiers.org/hco/10/GRCh38#132204793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138680769-C-A

132204948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680922-T-A

132204948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680922-T-C

http://identifiers.org/hco/10/GRCh38#132204967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138680942-A-C

132204983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680959-G-A

132204983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680959-G-T

132205028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680994-G-A

132205028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138680994-G-T

132205112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681079-C-T

132205114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681081-T-A

132205114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681081-T-C

132205152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681116-G-A

132205152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681116-G-T

132205304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681239-C-T

132205322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681247-G-A

132205427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681382-G-A

132205427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681382-G-T

132205458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681414-T-C

132205485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681442-G-T

132205572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681519-G-T

132205694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681653-C-G

132205694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681653-C-T

132205695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681654-G-A

132205695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681654-G-C

132205747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3016
most severe consequence: 3 prime UTR variant
orthologous variants: 138681712-G-A