http://identifiers.org/hco/1/GRCh38#59987356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96608151-C-A

59987376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96608176-A-G

59987662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96608434-G-T

59987663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96608435-G-A

59987859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96608697-G-A

http://identifiers.org/hco/1/GRCh38#59987975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96608803-C-A

59988123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96608933-C-G

59988355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609844-C-G

59988355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609844-C-T

http://identifiers.org/hco/1/GRCh38#59988359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96609848-C-A

59988359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609848-C-G

59988359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609848-C-T

59988367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609856-C-G

59988367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609856-C-T

59988369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609858-C-G

59988394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609884-T-G

59988397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96609887-G-A

59988666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96610125-G-T

http://identifiers.org/hco/1/GRCh38#59988796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96610241-C-A

59988812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96610256-G-A

http://identifiers.org/hco/1/GRCh38#59989017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96610445-C-A

59989145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 96610569-C-T

59989334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96610725-A-G

59989397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96610775-C-T

59989633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96610909-A-G

http://identifiers.org/hco/1/GRCh38#59989774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96611046-C-A

59989822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611094-G-T

59989829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611101-G-T

http://identifiers.org/hco/1/GRCh38#59989855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96611128-C-A

http://identifiers.org/hco/1/GRCh38#59989945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96611197-C-A

59989945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611197-C-G

http://identifiers.org/hco/1/GRCh38#59989958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96611207-C-A

59990161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611396-A-G

59990161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611396-A-T

59990224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611645-T-G

59990283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611779-G-A

59990283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611779-G-C

59990283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611779-G-T

59990298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611793-G-A

59990298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611793-G-T

59990340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611835-G-C

59990342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611837-G-T

59990349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non coding transcript exon variant
orthologous variants: 96611843-G-A

59990623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96612075-G-A

http://identifiers.org/hco/1/GRCh38#59990820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96612271-C-A

59990866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96612315-T-C

59990872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96612329-G-A

59990872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96612329-G-T

59990909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96612363-G-T

59991045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96612477-G-T

59994248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96613574-A-T

59994301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96613620-C-T

59994460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96613760-G-A

59994496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96613796-A-G

59994770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614029-C-T

59994781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614040-A-G

59994984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614238-C-T

59994998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614252-G-C

59995153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614412-C-G

http://identifiers.org/hco/1/GRCh38#59995305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96614515-C-A

59995473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614690-T-C

59995503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614730-T-C

59995619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96614846-G-T

59996216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96615535-G-T

59996217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96615536-A-G

59997150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96615916-G-A

59997173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96615927-G-T

59997315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616074-G-A

59997315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616074-G-T

59997430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616170-G-A

59997543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96616271-G-A

59997583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96616325-T-C

59997583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96616325-T-G

59997604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96616350-T-A

59997682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96616428-C-G

59997682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 96616428-C-T

59997684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96616430-C-T

59997769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 96616512-A-G

59997853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96616600-C-T

59997941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616684-G-A

59997941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616684-G-T

59997961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616704-G-A

59997961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616704-G-T

59997977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616713-T-A

59997977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616713-T-G

59998034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616765-G-C

59998103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616832-G-T

http://identifiers.org/hco/1/GRCh38#59998237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96616936-A-C

59998237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96616936-A-T

59998533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617232-G-A

59998533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617232-G-T

59998599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617303-A-G

59998994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617565-A-G

59999035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617593-T-C

59999175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617737-T-C

59999281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617838-C-G

59999281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96617838-C-T

59999577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618096-A-T

http://identifiers.org/hco/1/GRCh38#59999701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96618204-A-C

60000085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618586-T-C

60000340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618852-A-G

60000385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618897-T-C

60000396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618907-G-C

60000466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96618977-G-A

60000511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619021-A-G

60000770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619295-G-T

60000976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619496-G-A

60000976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619496-G-T

60001118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96619648-G-C

60001118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96619648-G-T

http://identifiers.org/hco/1/GRCh38#60001143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96619663-C-A

60001143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96619663-C-T

60001175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619691-A-G

60001220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619736-T-A

60001220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619736-T-C

60001220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619736-T-G

60001279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619780-G-A

60001279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619780-G-T

http://identifiers.org/hco/1/GRCh38#60001282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96619782-C-A

60001296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96619796-G-A

60001580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96620076-G-C

60001674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96620156-G-A

60002270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96620555-C-T

60003716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96621672-G-A

60003788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96621739-T-C

http://identifiers.org/hco/1/GRCh38#60003916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96621849-C-A

60003950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96621883-C-T

60004003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96621924-G-A

60004021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96621942-C-T

60004088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96622013-A-G

60004288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96623257-A-G

60004619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96623615-C-T

60004643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96623639-C-T

60004659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96623655-G-A

60004771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96623783-A-G

60005082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624097-G-T

60005284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624289-G-A

60005284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624289-G-C

http://identifiers.org/hco/1/GRCh38#60005449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96624483-C-A

60005449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624483-C-T

60005863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624841-G-A

60005868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624848-T-C

60005933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96624911-T-A

60006069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625052-T-G

60008825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96625581-C-T

60008844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96625600-G-C

60008864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625620-T-C

60008916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625671-G-C

60008917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625672-G-C

60008917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625672-G-T

60008926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625681-G-C

60008926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625681-G-T

http://identifiers.org/hco/1/GRCh38#60008956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96625711-C-A

60008956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625711-C-T

60009018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625775-C-T

60009035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625792-A-G

60009081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96625841-C-G

60009311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626026-G-A

60009455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626172-A-G

60009478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626195-A-G

60009810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626462-A-G

60009810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626462-A-T

60009838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626489-T-C

60009936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626587-G-T

60009985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626632-A-T

60010260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626920-G-C

60010260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626920-G-T

60010274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96626924-A-G

60010380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627200-A-G

60010389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627209-C-T

60010434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96627254-G-A

60010465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627285-G-C

60010470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627290-G-T

http://identifiers.org/hco/1/GRCh38#60010489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96627310-C-A

60010721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627542-C-G

60010721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627542-C-T

http://identifiers.org/hco/1/GRCh38#60010733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96627557-C-A

60010733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627557-C-G

60010735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96627559-G-T

http://identifiers.org/hco/1/GRCh38#60010897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96627844-A-C

60010925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96627869-G-A

60010925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96627869-G-C

60010925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96627869-G-T

60010934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96627878-G-A

60010934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96627878-G-T

60010968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96627911-T-C

60011022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96627964-A-T

60011036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96627978-G-A

60011044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96627986-T-C

60011147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628087-G-A

http://identifiers.org/hco/1/GRCh38#60011260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96628190-C-A

60011382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628306-C-T

60011383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628307-G-A

60011444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628364-C-G

60011444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628364-C-T

60011447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628367-C-T

60011448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96628368-A-T

60011565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629012-G-T

60011668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629108-G-A

60011668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629108-G-T

60011727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629166-T-C

60012221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629589-G-T

60012304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96629715-G-A

60017792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96634066-G-A

http://identifiers.org/hco/1/GRCh38#60017838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96634112-C-A

60017938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96634228-T-C

60018651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96634823-G-A

60018980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635080-A-G

60018998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635093-G-C

60019004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635099-G-A

60024583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635889-G-A

60024660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635961-C-G

60024660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96635961-C-T

60024820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96636116-C-T

http://identifiers.org/hco/1/GRCh38#60025549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96637523-A-C

http://identifiers.org/hco/1/GRCh38#60025556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96637530-C-A

60025556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96637530-C-T

60025603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96637557-A-G

60025815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96637729-T-C

60027723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96638789-A-G

60027782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96638848-T-C

60028004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639063-G-C

http://identifiers.org/hco/1/GRCh38#60028213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96639218-A-C

60028262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639267-G-C

60028459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639455-C-T

60028462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639458-T-C

60028490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639486-C-G

60028862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96639771-G-A

60030904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96640015-C-T

60031277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96640386-A-G

60031472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96640571-T-C

60031620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96640700-T-C

http://identifiers.org/hco/1/GRCh38#60031922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96640972-C-A

http://identifiers.org/hco/1/GRCh38#60032003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96641039-C-A

60032003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96641039-C-T

60032072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96641108-A-G

60032073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96641109-T-C

http://identifiers.org/hco/1/GRCh38#60033100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96641840-A-C

http://identifiers.org/hco/1/GRCh38#60033188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96641927-C-A

60033364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642100-G-A

60033364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642100-G-T

http://identifiers.org/hco/1/GRCh38#60033393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96642202-C-A

60033393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642202-C-G

60033393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642202-C-T

60033395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642204-G-A

60033395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642204-G-T

http://identifiers.org/hco/1/GRCh38#60033436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96642260-C-A

60033436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642260-C-T

60033488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96642305-G-A

http://identifiers.org/hco/1/GRCh38#60033497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96642314-A-C

60033640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 96642457-T-A

60033640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 96642457-T-C

60033640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 96642457-T-G

60033679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642494-T-C

60033685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642500-C-T

60033703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642519-T-C

60033703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642519-T-G

60033717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642533-T-C

60033727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642543-G-A

60033727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642543-G-T

60033738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642552-T-C

60033738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642552-T-G

60033784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642584-C-G

60033813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96642615-A-G

http://identifiers.org/hco/1/GRCh38#60034060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96642862-A-C

60034294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96643085-G-C

http://identifiers.org/hco/1/GRCh38#60034337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96643121-A-C

60034339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96643123-G-T

http://identifiers.org/hco/1/GRCh38#60035384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96643328-A-C

60035593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96643457-G-A

60036066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96643895-T-C

http://identifiers.org/hco/1/GRCh38#60037905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96646084-C-A

http://identifiers.org/hco/1/GRCh38#60038105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96646291-C-A

60038105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 96646291-C-G

60038105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 96646291-C-T

60038126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646312-A-G

http://identifiers.org/hco/1/GRCh38#60038165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96646352-C-A

60038165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646352-C-G

60038165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646352-C-T

60038228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646420-A-T

60038231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646423-T-A

60038231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646423-T-C

60038231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646423-T-G

60038288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96646469-C-T

http://identifiers.org/hco/1/GRCh38#60038291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96646472-A-C

60039049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96649419-G-A

60039830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650010-G-T

60039863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650044-T-A

60039868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650049-G-T

60039910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 96650091-G-A

http://identifiers.org/hco/1/GRCh38#60039911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96650092-C-A

60039992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96650173-C-T

60040006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650187-G-A

60040081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96650262-A-G

60040102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650283-G-A

60040102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650283-G-T

60040141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650322-C-T

60040154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96650335-T-A

60040154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96650335-T-G

60040155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650336-G-A

60040155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, missense_variant
orthologous variants: 96650336-G-T

60040166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 96650347-G-A

60040230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650403-A-G

60040266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650434-T-C

60040372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650534-C-T

60040557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650717-G-C

http://identifiers.org/hco/1/GRCh38#60040589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96650749-C-A

60040688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650816-A-T

60040730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650857-T-C

60040743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96650870-A-G

60041147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651133-A-G

60041147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651133-A-T

60041162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651148-G-A

http://identifiers.org/hco/1/GRCh38#60041165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96651151-C-A

60041165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651151-C-G

60041165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651151-C-T

60041209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651191-T-C

60041224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651206-A-T

60041611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651562-A-G

60041709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651657-G-A

60041709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651657-G-T

60041733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651682-C-T

60041781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651709-C-T

60041792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651720-T-A

60041792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96651720-T-G

http://identifiers.org/hco/1/GRCh38#60041890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96651782-C-A

60042416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652168-C-G

60042487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652225-A-G

60042487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652225-A-T

http://identifiers.org/hco/1/GRCh38#60042492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96652230-C-A

http://identifiers.org/hco/1/GRCh38#60042521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96652260-C-A

60042662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652381-C-G

60042721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652434-G-A

60042843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652619-T-C

60042852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652628-G-A

60042852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652628-G-C

60043025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96652799-G-A

60051530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653523-C-G

60051530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653523-C-T

60051557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653548-A-G

http://identifiers.org/hco/1/GRCh38#60051695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96653679-C-A

60051695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653679-C-G

60051753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653738-G-T

60051758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653743-T-C

60051812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653797-C-T

60051819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653806-G-T

60051940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96653926-C-T

60052013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96654002-G-A

60052062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96654051-A-G

60053314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96655217-T-C

http://identifiers.org/hco/1/GRCh38#60053318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96655221-C-A

60055021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96657648-G-A

60055021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96657648-G-C

60055181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96657803-C-T

60055190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96657812-T-C

60055230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense variant
orthologous variants: 96657852-T-C

60055262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense variant
orthologous variants: 96657884-G-A

60055295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense variant
orthologous variants: 96657917-T-C

60055299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense variant
orthologous variants: 96657921-C-T

60055300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: synonymous variant
orthologous variants: 96657922-A-G

60055752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96658361-T-C

60055752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96658361-T-G

60057097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96658708-G-C

60057309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96658908-T-A

60057323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96658922-G-A

60057755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659294-G-A

60057755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659294-G-T

60057872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659399-A-G

60058191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659719-G-C

60058261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659786-C-G

http://identifiers.org/hco/1/GRCh38#60058293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96659818-A-C

60058340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96659898-T-C

http://identifiers.org/hco/1/GRCh38#60058488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96660112-C-A

60058488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96660112-C-G

60058535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96660163-A-T

http://identifiers.org/hco/1/GRCh38#60058601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96660218-C-A

http://identifiers.org/hco/1/GRCh38#60058743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96660337-C-A

http://identifiers.org/hco/1/GRCh38#60059096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96660986-A-C

60059156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661046-G-A

60059231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661120-T-G

60059773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661629-A-G

60059976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661828-G-A

60059976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661828-G-T

60060010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661865-C-T

60060055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96661914-T-C

60060175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96662112-A-G

60062659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96666474-T-G

60068161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96668971-A-G

60068165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96668975-C-T

60068229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669034-G-T

60068238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669043-C-T

60068260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669062-T-C

60068276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669078-C-T

60068365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669158-A-G

60068392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669185-A-G

60068405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669197-A-G

60068617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669773-C-T

60068793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96669957-C-T

60068869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96670032-T-C

http://identifiers.org/hco/1/GRCh38#60069459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96670572-C-A

60069459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96670572-C-T

60069759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96670815-G-C

60069945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96671051-G-A

http://identifiers.org/hco/1/GRCh38#60070022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96671102-C-A

60070443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96671456-G-A

60070706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96671672-G-A

60070870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96671763-T-C

60070924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96671813-G-A

60071476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672332-T-A

60071514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672369-C-T

60071574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672423-T-C

60071617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672448-C-T

60071639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672473-T-C

60071945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96672716-C-T

60072389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96673157-T-C

60072443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96673211-G-T

60072505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96673258-G-C

60072505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96673258-G-T

60072537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 96673291-A-G

60072553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: missense variant
orthologous variants: 96673307-C-T

60072635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: synonymous variant
orthologous variants: 96673389-T-C

60072971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674236-C-T

http://identifiers.org/hco/1/GRCh38#60073056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96674320-C-A

http://identifiers.org/hco/1/GRCh38#60073119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#96674384-C-A

60073189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674451-G-A

60073221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674474-C-G

60073278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674539-G-A

60073643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674887-G-T

60073669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: intron variant
orthologous variants: 96674918-G-T

60073697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: 5 prime UTR variant
orthologous variants: 96674949-G-T

60073723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: 5 prime UTR variant
orthologous variants: 96674976-A-G

60073738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: 5 prime UTR variant
orthologous variants: 96674988-G-A

60073738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28547
most severe consequence: 5 prime UTR variant
orthologous variants: 96674988-G-T