69013206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87312668-G-A

69013206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87312668-G-C

69013206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87312668-G-T

http://identifiers.org/hco/2/GRCh38#69013240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87312635-C-A

69013283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87312607-G-C

69013375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87312517-G-A

69013439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87312461-G-A

69013439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87312461-G-T

69013506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87312416-A-G

http://identifiers.org/hco/2/GRCh38#69013545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87312383-C-A

69013545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87312383-C-T

69013911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87312156-C-T

69014335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87311803-C-T

http://identifiers.org/hco/2/GRCh38#69014375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87311763-C-A

69014375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87311763-C-T

69014554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87311597-C-G

69014815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87311348-G-A

69015248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87310983-A-G

http://identifiers.org/hco/2/GRCh38#69015262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87310969-C-A

69015262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87310969-C-T

69015486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87310722-G-T

69016136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87310049-C-T

69016455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87309761-T-C

69016788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308852-A-T

69016833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308813-G-A

69017151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308607-T-G

69017494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308281-T-C

69017720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308070-T-C

69017781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87308009-G-A

69017797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87307993-A-G

69017813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87307984-G-A

69017824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87307973-G-A

http://identifiers.org/hco/2/GRCh38#69017826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87307971-C-A

69018734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87307296-C-T

http://identifiers.org/hco/2/GRCh38#69018799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87307229-A-C

69018799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87307229-A-G

69018877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87307031-C-T

69019181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87306721-G-A

69020388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87306501-G-A

69020797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87306119-T-C

69020831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87306084-C-T

69020889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87306016-T-C

69021674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87305401-A-T

69021847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87305246-C-T

69021986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87305118-T-C

69021989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87305115-G-T

69022149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304890-C-T

69022405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304637-C-T

69022463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304566-C-T

69022466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304563-A-G

69022802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304033-C-G

69022802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87304033-C-T

http://identifiers.org/hco/2/GRCh38#69022827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87304008-A-C

69023011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303847-A-T

http://identifiers.org/hco/2/GRCh38#69023059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87303779-C-A

69023059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303779-C-T

69023113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303732-G-A

69023194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303644-C-G

69023358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303457-T-C

69023408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87303383-G-A

69024235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87302346-A-G

69024327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87302254-G-A

69024436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87302139-A-G

http://identifiers.org/hco/2/GRCh38#69024523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87302053-C-A

69024523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87302053-C-G

69024575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87302008-G-C

69024619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301964-C-T

69024649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301933-C-T

69024999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301579-C-G

69025013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301565-T-C

69025037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301541-T-C

69025091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301490-A-G

69025122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87301468-G-A

69025804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87300892-T-C

69025894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87300804-G-C

69026228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87300510-G-T

69026248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87300487-T-C

69026476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87300403-A-G

69027012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299703-T-A

69027255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299469-G-A

69027260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299464-G-C

69027469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299290-G-A

69027606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299152-G-A

69027642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87299116-G-A

69027800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87298996-A-T

69027801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87298995-G-A

69027922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87298903-A-G

69028023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87298813-G-A

69028076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87298761-T-A

http://identifiers.org/hco/2/GRCh38#69028174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87298684-A-C

69028828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297927-A-G

69029579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297474-C-T

69029741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297303-C-T

69029749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297295-A-G

69029885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297182-T-C

69029898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297169-A-G

69029992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87297088-A-G

69030075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87297010-A-G

69030147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296929-C-T

69030338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296776-C-T

69030557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296576-T-G

69030663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296443-A-G

http://identifiers.org/hco/2/GRCh38#69030672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87296434-C-A

69030769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296340-T-C

69031078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296037-C-G

69031078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87296037-C-T

69031367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87295717-A-G

69031438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87295662-T-C

69031511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87295604-G-A

69031577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87295535-A-G

69031995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87295367-C-T

69032113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87295247-T-C

69032418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294848-G-A

69032491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294776-A-G

69032597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294677-A-G

69032656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294629-G-C

69032798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294363-G-A

69033084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87294073-A-G

69033225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293932-A-G

69033225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293932-A-T

69033521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293791-A-G

69033578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293763-G-A

69033726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293627-C-G

69033778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293581-C-T

69033905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293530-A-G

69034031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293411-C-T

http://identifiers.org/hco/2/GRCh38#69034040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87293398-C-A

http://identifiers.org/hco/2/GRCh38#69034042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87293396-C-A

69034042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293396-C-G

69034206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293229-G-A

69034237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293196-A-G

69034371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87293065-C-T

69035025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87292595-G-A

69035236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87292395-G-A

69035236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87292395-G-T

69039168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87290522-G-C

69039243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87290461-T-C

69039529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87290112-A-G

69039706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289666-T-C

69039750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289622-G-A

69039810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289566-G-A

69040034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289383-G-A

69040034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289383-G-C

69040094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87289324-A-T

http://identifiers.org/hco/2/GRCh38#69040187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87289241-C-A

69040187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289241-C-T

69040199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289229-A-G

http://identifiers.org/hco/2/GRCh38#69040203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87289225-A-C

69040700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87289015-T-A

69040724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87288987-G-T

69040794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87288943-T-A

69043998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87285983-T-C

69044690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87285431-T-C

69044690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87285431-T-G

69044695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87285426-T-C

69044831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285290-C-T

69044860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285261-G-A

69044860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285261-G-T

69044908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285220-A-G

69044965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285173-A-G

69044986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285152-C-T

69045118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87285017-A-T

69045718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87284108-T-G

69045803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87284059-G-T

69046305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87283341-A-G

69046324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87283326-G-T

69046339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87283316-A-G

69046492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87283199-G-C

69046503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87283188-A-G

69046514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87283177-G-A

69046788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87283013-A-T

69047843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87280731-A-G

69048029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87280563-A-T

69048502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87280109-A-G

69048905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87279720-T-C

69049126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87279522-C-T

69049172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87279483-A-G

69049172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87279483-A-T

69052948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87278903-T-C

http://identifiers.org/hco/2/GRCh38#69053038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87278714-A-C

69053186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87278562-C-T

69053244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87278540-T-C

69053373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87278396-T-C

69053490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87278083-C-T

http://identifiers.org/hco/2/GRCh38#69053602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87277917-A-C

69053602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87277917-A-G

69053764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87277756-T-G

69053931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87277595-A-G

69054097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87277457-C-T

69054252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87277308-C-T

69055008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276807-T-C

69055192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276661-G-A

69055209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276645-T-G

69055301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276555-G-T

69055465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276388-T-C

69055495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276371-T-A

69055708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87276140-T-C

69055903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87275995-G-T

69055979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87275946-T-A

69056131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87275808-G-T

http://identifiers.org/hco/2/GRCh38#69056337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87275554-C-A

69056511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87275394-T-C

69056677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87275254-A-T

69064363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87272452-G-A

69064440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87272388-C-T

69064561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87272283-A-T

69064721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87272128-C-G

69064963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271931-A-G

69065004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271897-A-G

http://identifiers.org/hco/2/GRCh38#69065129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87271756-A-C

69065129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271756-A-G

69065606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271328-T-C

69065659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271288-T-C

69065868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271122-G-C

69065894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87271096-G-T

http://identifiers.org/hco/2/GRCh38#69065912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87271082-A-C

69066225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270865-A-G

69066603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270756-G-A

69066606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270753-G-A

69066613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270746-T-C

69066789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270602-A-G

69067316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270145-A-G

69067322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270118-G-A

69067322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270118-G-T

69067367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270071-T-A

69067367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270071-T-C

69067369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87270069-T-C

http://identifiers.org/hco/2/GRCh38#69067432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87270012-A-C

http://identifiers.org/hco/2/GRCh38#69067483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87269969-A-C

69067517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87269935-C-T

69067545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87269907-G-C

69067817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87268208-C-T

69068188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267871-A-T

69068655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267659-A-G

69068942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267407-G-A

69069006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267345-G-A

69069068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267286-C-T

69069090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267259-G-A

69069250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267071-G-C

69069304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87267017-C-G

69069370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266947-T-C

69069994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266449-A-G

69070116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266328-G-A

69070158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266297-T-A

69070249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266209-T-C

69070380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266065-T-C

69070403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87266043-T-A

69070473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265976-T-C

http://identifiers.org/hco/2/GRCh38#69070535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87265924-C-A

69070548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265911-G-A

69070548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265911-G-T

69070751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265713-T-G

http://identifiers.org/hco/2/GRCh38#69070752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87265712-C-A

69070752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265712-C-T

69070927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265560-C-G

69070993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265495-A-T

69071011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265476-A-T

http://identifiers.org/hco/2/GRCh38#69071596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87265333-A-C

69071596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265333-A-T

69071602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265327-G-A

69071656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265274-T-C

69071671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265260-A-G

69071684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265249-T-G

http://identifiers.org/hco/2/GRCh38#69071711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87265219-A-C

69071715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265215-G-A

http://identifiers.org/hco/2/GRCh38#69071913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87265051-C-A

69071932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87265033-G-A

69072230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264740-G-A

69072665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264329-G-A

http://identifiers.org/hco/2/GRCh38#69072768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87264275-A-C

69072768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264275-A-G

69072778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264265-G-A

69072918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264162-G-T

http://identifiers.org/hco/2/GRCh38#69073004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87264078-C-A

69073004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264078-C-G

69073004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87264078-C-T

69073030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87264052-A-G

69073120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263964-G-A

69073146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263943-G-A

69073146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263943-G-T

69073193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263849-G-C

69073193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263849-G-T

69073224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263820-A-G

69073224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263820-A-T

69073427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263653-C-T

69073428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263632-A-G

69073430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87263630-T-G

69074319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87262515-A-G

69074474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87262366-T-G

69074639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87262217-T-C

69074672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87262183-A-G

69074874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87262002-C-G

69074980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261887-T-C

69075001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261867-C-G

69075118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261772-G-A

69075133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261758-T-C

69075183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261706-T-C

69075338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261559-C-T

69075506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261379-A-G

69075540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261352-T-A

69075540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261352-T-C

69075565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87261327-A-G

69075664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261228-G-A

69075664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261228-G-T

69075733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261162-G-C

69075775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261122-T-C

69075789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261109-A-G

69075795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87261103-G-A

69076601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87260468-A-G

http://identifiers.org/hco/2/GRCh38#69076771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87260321-A-C

69077164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259976-G-A

http://identifiers.org/hco/2/GRCh38#69077181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259959-A-C

69077210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259932-G-C

69077210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259932-G-T

69077231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259913-T-C

http://identifiers.org/hco/2/GRCh38#69077255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259889-C-A

69077291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259866-A-G

http://identifiers.org/hco/2/GRCh38#69077299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259858-C-A

69077354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259797-C-T

69077370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87259780-A-T

http://identifiers.org/hco/2/GRCh38#69077560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259597-A-C

69077560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87259597-A-G

69077562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87259595-T-C

http://identifiers.org/hco/2/GRCh38#69077563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259594-C-A

http://identifiers.org/hco/2/GRCh38#69077594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87259569-A-C

69077594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87259569-A-G

69077747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87259425-C-T

69079381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87258754-C-G

69079528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87258625-T-C

69079619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87258534-G-C

69080463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87257068-C-T

69080857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256616-T-C

69080857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256616-T-G

69081042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256444-T-C

69081081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256374-C-T

69081148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256301-C-T

69081348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256127-G-T

69081390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87256089-C-T

69081503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87255999-T-C

69081763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87255810-C-T

69082280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87255367-G-T

69082573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87254925-G-T

69082772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87254757-G-A

69083025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87254544-C-T

69083236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87254339-A-G

69083331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87254265-G-A

69084078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253608-T-C

69084143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253563-C-T

69084249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253425-T-C

69084278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253396-T-C

69084568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253242-T-C

69085479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87253027-A-G

http://identifiers.org/hco/2/GRCh38#69085605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87252908-C-A

69085853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252672-A-G

69085857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252668-A-G

69085866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252659-G-A

69085891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252634-G-A

69085891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252634-G-C

69085953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252579-T-C

69086015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252518-G-A

http://identifiers.org/hco/2/GRCh38#69086114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87252424-A-C

69086177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87252371-G-A

69086439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87252120-C-G

69086467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87252043-A-T

69086750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251602-A-G

69086786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251578-G-A

69086786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251578-G-T

69086794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251571-T-A

69086798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251567-C-T

69086844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251524-T-C

69086937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251438-C-T

69086995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251142-A-T

69087060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251084-G-A

69087089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87251059-G-A

69087414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87250758-C-G

69087619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87250190-C-T

69087767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87249560-C-T

69087780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87249544-C-T

69088048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87249260-T-G

69088227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87249082-T-C

69088487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87248821-G-A

69088890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87248512-A-G

69088890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87248512-A-T

69089068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87248353-G-A

69089095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87248328-C-G

69089475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247643-C-T

69089505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247613-T-A

69089586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247561-A-G

69089780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247373-G-C

69089980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247209-C-T

69090035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247169-C-G

69090131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247089-C-G

69090204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87247014-G-A

69090535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87246667-G-T

69090705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87246415-G-A

69090705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87246415-G-T

http://identifiers.org/hco/2/GRCh38#69090770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87246358-C-A

69090913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87246229-G-A

69090913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87246229-G-T

http://identifiers.org/hco/2/GRCh38#69090992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87246153-C-A

69090992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87246153-C-T

69091016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87246129-G-T

69091101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87246052-G-A

69091827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245510-C-T

69092055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245335-G-C

69092089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245301-G-C

69092161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245232-G-A

69092268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245163-A-G

http://identifiers.org/hco/2/GRCh38#69092374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87245056-A-C

69092425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87245002-T-C

69092446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244927-C-T

69092489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244880-A-T

69092501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244864-T-C

69092503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244862-G-A

69092537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244832-G-A

69092572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244797-T-G

69092605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87244767-A-G

69093295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87239436-A-T

69096778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238801-C-T

http://identifiers.org/hco/2/GRCh38#69096802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87238778-A-C

69096853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238734-C-T

69096859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238728-T-G

69097030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238596-T-G

69097031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238595-A-G

69097111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238510-C-G

69097112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238509-C-T

69097188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238467-C-T

69097205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238452-C-T

69097320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87238349-A-T

69098218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87236767-T-C

69098269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87236716-T-C

69099172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87236241-T-A

69099278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87236136-T-G

http://identifiers.org/hco/2/GRCh38#69099900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87235799-A-C

69100374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87235313-G-T

69100484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87235231-C-T

69100914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234853-C-T

69101115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234663-T-A

69101163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234621-C-T

69101282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234550-A-G

69101428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234445-G-A

69101447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234427-A-G

http://identifiers.org/hco/2/GRCh38#69101465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87234410-A-C

69101529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234347-G-C

69101632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234254-G-A

69101665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234219-A-G

69101736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87234156-A-G

69102004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233577-C-T

69102006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233575-T-A

69102404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233208-T-A

69102420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233192-T-C

69102574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233063-G-T

69102652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233029-G-T

69102665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233016-G-A

http://identifiers.org/hco/2/GRCh38#69102696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87233003-C-A

69102696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87233003-C-T

69102712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87232987-G-A

69102712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87232987-G-C

69102712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87232987-G-T

69102775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87232924-T-A

69102798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87232902-G-A

http://identifiers.org/hco/2/GRCh38#69102813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87232887-A-C

69102934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87232769-A-G

69102947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87232756-C-G

69102976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87232740-A-G

http://identifiers.org/hco/2/GRCh38#69103016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87232711-C-A

69103016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87232711-C-T

69103041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232686-G-A

69103055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232670-T-C

69103113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232551-A-G

69103113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232551-A-T

69103142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232523-T-A

69103142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232523-T-C

69103142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232523-T-G

http://identifiers.org/hco/2/GRCh38#69103176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87232489-A-C

69103176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232489-A-G

69103176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232489-A-T

http://identifiers.org/hco/2/GRCh38#69103186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87232479-C-A

69103186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232479-C-G

69103269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232419-C-T

http://identifiers.org/hco/2/GRCh38#69103289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87232402-C-A

69103289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232402-C-T

69103292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232399-T-G

69103302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232396-G-A

69103302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232396-G-C

69103302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232396-G-T

69103329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232369-G-A

69103329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87232369-G-T

69103625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87232075-A-G

69103641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87232059-A-G

69103693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87232008-A-T

69103873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87231840-G-T

http://identifiers.org/hco/2/GRCh38#69103901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87231822-C-A

69103912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87231813-C-T

69104334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87231680-G-T

69107981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230960-C-G

69108158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230782-A-T

69108188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230752-C-G

69108188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230752-C-T

69108206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230734-G-C

69108894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230159-A-T

69109044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87230029-G-T

69109146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87229937-G-A

69109285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87229797-T-C

69109292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87229790-G-A

69109470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87229605-C-T

http://identifiers.org/hco/2/GRCh38#69109642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87229467-C-A

69110217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87228720-G-A

69111048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87228090-T-C

69111423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227714-A-G

69111546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227640-A-G

69111635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227560-T-C

69111635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227560-T-G

69111653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227541-T-G

69111676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227415-T-C

69111678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227413-T-C

69111884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227116-G-A

69111884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227116-G-T

69111896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227094-G-A

69111955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87227040-T-C

http://identifiers.org/hco/2/GRCh38#69112009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87226990-C-A

69112009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226990-C-T

http://identifiers.org/hco/2/GRCh38#69112029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87226970-A-C

69112090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226919-C-T

69112101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226909-G-A

69112101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226909-G-C

69112101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226909-G-T

69112247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226774-C-T

69112277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226741-T-C

http://identifiers.org/hco/2/GRCh38#69112737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87226384-A-C

69112762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226359-C-T

69113094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226098-T-C

69113178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87226002-A-T

69113248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225933-G-A

69113461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225734-C-T

69113485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225710-C-T

69113532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225666-A-G

69113553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225634-G-A

69113554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225633-G-C

69113562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225625-G-A

69113562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225625-G-T

69113674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225534-T-C

69114098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225107-A-G

69114157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87225050-C-T

http://identifiers.org/hco/2/GRCh38#69114421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87224606-A-C

69114722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224334-C-T

69114752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224304-A-G

69114960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224120-C-T

69115016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224083-C-T

http://identifiers.org/hco/2/GRCh38#69115039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87224060-C-A

69115039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224060-C-T

69115080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224048-G-A

69115080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87224048-G-T

69115265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223919-C-T

http://identifiers.org/hco/2/GRCh38#69115305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87223847-A-C

69115321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223831-G-A

69115379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223785-C-T

69115448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223716-T-C

69115550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223618-C-T

69116874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223272-G-A

69116904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223242-T-C

69117005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223147-A-G

69117007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87223145-C-T

http://identifiers.org/hco/2/GRCh38#69117121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87223039-A-C

http://identifiers.org/hco/2/GRCh38#69117122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87223038-C-A

69117309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222942-T-C

69117371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222873-A-T

69117502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222729-C-T

69117552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222698-T-G

69117634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222620-T-A

69117825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222446-T-G

69117865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222404-A-T

69118516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87222078-C-T

69118612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221973-A-G

69118684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221904-G-A

69118750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221829-A-T

69119094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221503-G-T

69119096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221501-G-T

69119175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221423-G-A

69119269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221404-G-A

69119269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221404-G-T

69119270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221403-C-T

69119277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221396-G-A

69119559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221148-G-C

69119596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221119-G-A

69119596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221119-G-C

69119597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87221118-G-A

69123121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87219429-G-A

http://identifiers.org/hco/2/GRCh38#69123210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87219349-C-A

69123210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87219349-C-T

69123283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87219287-T-C

69123393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87219199-G-A

69123534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87219064-C-G

69123622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87218991-C-T

69123953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87218730-G-A

69123955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87218728-T-C

http://identifiers.org/hco/2/GRCh38#69124097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87218611-A-C

69124106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87218602-A-G

69124112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87218596-T-C

http://identifiers.org/hco/2/GRCh38#69124508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87218063-A-C

http://identifiers.org/hco/2/GRCh38#69124678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87217907-A-C

69124727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217855-G-A

69124727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217855-G-T

69124807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217796-T-C

69125018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217604-G-A

69125045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217548-T-C

69125079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217515-G-A

69125079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87217515-G-T

http://identifiers.org/hco/2/GRCh38#69125295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87217287-C-A

69125857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216807-A-T

69125905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216759-G-A

http://identifiers.org/hco/2/GRCh38#69125922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87216743-C-A

69125930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216735-A-G

69126049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216631-T-C

69126192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216486-C-T

69126251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216451-C-T

69126305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216400-T-C

69126307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216398-G-A

69126416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216291-T-C

69126417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216290-G-A

69126567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216154-A-T

69126640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216089-A-G

69126712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216018-T-A

69126715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87216016-T-C

69126751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215979-A-G

69126756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215974-T-C

69126820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215928-T-G

69126908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215832-T-G

69126918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215822-C-T

69126983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215744-C-T

69127491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215342-G-C

69127595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215254-G-A

69127773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215168-T-A

http://identifiers.org/hco/2/GRCh38#69127839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87215124-A-C

69127839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215124-A-G

69127848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87215115-A-G

69128514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87214673-C-T

69128548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87214640-G-A

69128700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87214499-C-T

69129081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87214134-A-G

69129093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87214123-C-G

69129267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213989-T-A

69129390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213860-G-A

69129413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213840-A-G

http://identifiers.org/hco/2/GRCh38#69129459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87213795-A-C

69129506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213730-C-T

69129549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213677-C-G

69129549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213677-C-T

69129620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213635-G-A

69129644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87213611-A-G

69130116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant
orthologous variants: 87213216-C-T

69130251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87213075-A-G

http://identifiers.org/hco/2/GRCh38#69130256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87213070-C-A

69130256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87213070-C-G

69130377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87212946-C-T

69130635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87212538-T-C

69130782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87212426-T-C

69130911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87212304-G-A

69131185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87210589-T-C

http://identifiers.org/hco/2/GRCh38#69132379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87210408-A-C

69132381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87210406-G-A

69132667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87210120-T-C

69132874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209906-C-T

69132941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209843-G-T

69133112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209751-C-T

69133292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209629-C-G

69133292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209629-C-T

69133310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209616-T-A

69133348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209579-C-T

69133457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209460-G-A

69133469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209445-T-C

69134429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209216-C-G

69134429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87209216-C-T

http://identifiers.org/hco/2/GRCh38#69135029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87208690-C-A

69135029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 87208690-C-T

69135048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 87208671-T-C

69135106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87208613-T-C

69135106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87208613-T-G

http://identifiers.org/hco/2/GRCh38#69135109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87208610-C-A

69135109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87208610-C-T

69135141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87208587-T-C

http://identifiers.org/hco/2/GRCh38#69135292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87208438-A-C

69135292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87208438-A-G

69135599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87208131-T-C

69136235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87207434-C-T

69136236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87207433-T-G

69136464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87207366-T-C

69136500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87207328-A-T

69136883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206751-T-A

69136951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206686-G-A

69136964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206673-T-G

69136968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206669-G-T

69136991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206647-A-T

69137080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206569-T-G

69137112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206543-A-G

69137163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206471-A-G

69137180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206454-A-G

69137385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206222-G-A

69137385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206222-G-T

69137390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87206217-T-C

69138436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87205261-A-G

69138529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87205170-A-G

69138662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87205047-A-G

69139071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87204696-A-T

69139136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87204630-A-G

69142554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203933-A-G

69142770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203760-C-T

69142905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203640-G-A

69142905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203640-G-T

http://identifiers.org/hco/2/GRCh38#69142930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87203611-C-A

http://identifiers.org/hco/2/GRCh38#69143037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87203508-A-C

69143261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203367-A-G

http://identifiers.org/hco/2/GRCh38#69143263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87203365-A-C

69143465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87203192-T-C

69143798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87202878-G-A

69143798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87202878-G-T

69143806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87202870-C-G

69144253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87202464-A-G

69144272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87202455-C-T

http://identifiers.org/hco/2/GRCh38#69144308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87202418-A-C

69144370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87202327-G-T

69144423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87202274-G-A

69144435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87202262-T-C

69145645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201965-C-T

69145649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201961-G-A

69145649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201961-G-T

69145654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201956-G-C

69145654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201956-G-T

69145707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201906-A-G

69145839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201785-G-A

69145839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201785-G-T

69145844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201779-A-T

http://identifiers.org/hco/2/GRCh38#69145860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87201763-C-A

69145860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201763-C-G

http://identifiers.org/hco/2/GRCh38#69145909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87201712-C-A

69145923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201698-A-G

69145923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87201698-A-T

http://identifiers.org/hco/2/GRCh38#69146106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87200513-C-A

69146106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200513-C-T

http://identifiers.org/hco/2/GRCh38#69146116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87200503-C-A

69146116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200503-C-T

69146181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200445-T-C

69146216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200410-G-A

69146216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200410-G-C

69146218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200408-A-G

69146218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200408-A-T

69146238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87200382-T-C

69146765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87199335-G-A

69146775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87199326-C-T

69146877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87199267-T-C

69147035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87199042-G-A

http://identifiers.org/hco/2/GRCh38#69147119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87198958-C-A

http://identifiers.org/hco/2/GRCh38#69147154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87198922-C-A

69147207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87198876-G-C

69147280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87198782-G-A

69148084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87198570-A-G

69148131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87198523-C-T

69148449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197820-G-T

69148478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197797-G-A

69148500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197768-G-A

69148553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197591-T-C

69148553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197591-T-G

69148555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197589-A-G

69148633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197507-T-C

http://identifiers.org/hco/2/GRCh38#69148648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87197494-C-A

69148703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197444-C-T

69148705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197442-T-C

69149124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197126-G-A

http://identifiers.org/hco/2/GRCh38#69149166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87197084-C-A

69149187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197070-C-T

69149224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197053-C-T

69149259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197040-G-C

http://identifiers.org/hco/2/GRCh38#69149261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87197038-C-A

69149261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87197038-C-T

69149819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87196568-G-C

69150394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87196032-G-A

69151948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194555-G-A

http://identifiers.org/hco/2/GRCh38#69151965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87194538-A-C

http://identifiers.org/hco/2/GRCh38#69152069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87194447-C-A

http://identifiers.org/hco/2/GRCh38#69152136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87194378-C-A

69152149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194368-C-G

69152226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87194292-G-T

69152340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194177-G-C

69152340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194177-G-T

69152346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194171-T-A

69152360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194156-T-C

69152380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87194139-T-C

69154074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87193823-T-C

69154435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87193472-C-G

69154458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87193449-A-G

69157908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87192147-T-C

69158007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87192070-C-G

69158125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191986-A-G

69158136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191975-C-T

http://identifiers.org/hco/2/GRCh38#69158204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87191920-A-C

69158218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191906-C-T

69158247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191870-G-A

69160039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191425-G-A

http://identifiers.org/hco/2/GRCh38#69160087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87191378-C-A

http://identifiers.org/hco/2/GRCh38#69160112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87191356-A-C

69160185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191290-A-G

69160204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87191261-G-A

69160257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191197-T-C

69160275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191170-G-A

69160276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191169-C-T

69160309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191132-C-G

69160352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87191089-T-A

http://identifiers.org/hco/2/GRCh38#69160396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87191045-C-A

http://identifiers.org/hco/2/GRCh38#69160761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87190721-A-C

69161065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190447-C-T

69161093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190420-G-A

69161203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190312-A-G

69161235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190287-A-T

69161488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190029-G-A

69161511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87190006-A-T

69161539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189982-A-G

69161568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189953-G-T

69161569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189952-C-T

http://identifiers.org/hco/2/GRCh38#69161573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87189948-C-A

69161637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189883-C-T

69161641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189879-T-G

69161834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189693-G-A

69161866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189659-G-T

69162150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189250-G-T

69162358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87189072-G-A

http://identifiers.org/hco/2/GRCh38#69162448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87188988-A-C

69162460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87188976-G-T

69162470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87188960-T-G

69163133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87188319-G-A

69163582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187887-C-T

69163641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187831-A-G

69163648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187824-G-A

69163648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187824-G-C

69163648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187824-G-T

69163685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187789-G-A

69163685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187789-G-T

69163820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187644-G-T

69163866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187598-G-A

69163931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187522-T-A

69164062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187383-G-A

69164065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187380-T-A

69164065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187380-T-C

69164108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187349-C-T

69164116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187341-A-G

69164362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187117-T-A

69164362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87187117-T-C

69164799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87186723-C-T

69167448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87184041-C-G

69167784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183825-C-T

69167790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183819-C-T

69168066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183205-C-G

69168189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183111-G-A

69168189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183111-G-C

69168189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183111-G-T

69168297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87183047-C-G

69168356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182988-A-G

http://identifiers.org/hco/2/GRCh38#69168444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87182922-C-A

69168444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182922-C-T

69168515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182870-C-T

69168520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182865-G-A

http://identifiers.org/hco/2/GRCh38#69168869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87182583-A-C

69169038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182425-C-T

69169284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87182219-A-T

69169622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181973-A-G

69169664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181926-T-C

69169725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181858-G-A

69169847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181750-C-G

69169870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181726-A-T

69169998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181620-C-G

69170030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181594-G-A

69170118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181533-A-T

69170127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181526-T-C

69170172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181496-A-T

http://identifiers.org/hco/2/GRCh38#69170184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87181490-C-A

http://identifiers.org/hco/2/GRCh38#69170209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87181465-A-C

69170237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87181441-T-C

69170314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, missense_variant
orthologous variants: 87181365-G-T

http://identifiers.org/hco/2/GRCh38#69170430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87181287-C-A

69170430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87181287-C-T

69170431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87181286-A-G

69170431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87181286-A-T

69170468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87181250-A-G

69170568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87180860-C-T

69170783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87180654-G-A

69170826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87180611-C-T

69171421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179921-A-G

69171517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179839-G-A

69171536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179818-G-A

69171737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179658-A-G

69171860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179576-T-A

69171860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87179576-T-C

69172504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 87179237-C-T

http://identifiers.org/hco/2/GRCh38#69172612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87178857-C-A

69172612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87178857-C-T

69172800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87171894-G-A

69172997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87171726-G-A

69173211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87171438-G-A

69173218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87171431-T-C

http://identifiers.org/hco/2/GRCh38#69173307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87171335-C-A

69173549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87171078-G-A

http://identifiers.org/hco/2/GRCh38#69173904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87170753-A-C

69173923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87170732-C-G

69173951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87170682-G-A

69174016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87170619-T-C

69174706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87169946-G-A

69175028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87169675-C-T

69176114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168712-C-T

69176128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168698-C-T

69176138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168689-G-A

69176138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168689-G-C

69176138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168689-G-T

69176438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168427-C-T

69176523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168357-G-A

69176528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87168352-T-G

http://identifiers.org/hco/2/GRCh38#69177488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87167712-C-A

69177547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87167655-G-A

69177547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87167655-G-C

69178006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87167207-G-T

http://identifiers.org/hco/2/GRCh38#69178300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87166930-A-C

69178471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87166758-T-G

http://identifiers.org/hco/2/GRCh38#69181650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165952-C-A

69181676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165926-A-G

http://identifiers.org/hco/2/GRCh38#69181704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165887-A-C

69181704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165887-A-G

69181704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165887-A-T

69181716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165875-T-C

http://identifiers.org/hco/2/GRCh38#69182051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165637-C-A

69182092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165597-G-A

69182092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165597-G-T

69182101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165588-A-T

69182147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165542-G-A

69182147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165542-G-T

69182180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165514-G-A

http://identifiers.org/hco/2/GRCh38#69182366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165367-C-A

69182366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165367-C-T

http://identifiers.org/hco/2/GRCh38#69182404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165342-C-A

69182404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165342-C-G

69182404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165342-C-T

69182434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165322-T-C

http://identifiers.org/hco/2/GRCh38#69182449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165305-A-C

http://identifiers.org/hco/2/GRCh38#69182451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87165303-C-A

69182451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87165303-C-G

69182496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87165251-C-T

69184316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87164230-G-A

69184364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87164188-G-T

69184653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87163928-C-T

69185081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87163414-C-G

http://identifiers.org/hco/2/GRCh38#69185677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87163159-C-A

69185677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87163159-C-T

69185964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162898-C-T

69185965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162897-A-G

69185970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162892-T-C

http://identifiers.org/hco/2/GRCh38#69186028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87162839-C-A

69186028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162839-C-T

http://identifiers.org/hco/2/GRCh38#69186037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87162830-C-A

69186101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, undefined
orthologous variants: 87162749-G-A

69186215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162646-G-A

69186216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87162645-G-A

69186829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161465-G-A

69186947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161360-G-A

http://identifiers.org/hco/2/GRCh38#69187017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87161300-C-A

69187030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161287-A-G

69187048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161269-C-T

69187083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161242-T-C

69187118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161207-G-A

69187153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161177-C-T

69187220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161100-C-T

69187236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87161084-T-C

69189022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87159847-C-T

69189510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87159111-G-A

69189834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87158904-T-C

69189968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87158768-C-T

69189992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87158745-C-T

69190068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87158680-T-A

69191133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87157755-T-C

http://identifiers.org/hco/2/GRCh38#69191342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87157560-C-A

69193194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87157324-A-G

69193221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87157298-G-T

http://identifiers.org/hco/2/GRCh38#69193286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87157219-C-A

69193341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87157164-C-T

69193412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: synonymous variant
orthologous variants: 87157093-C-T

http://identifiers.org/hco/2/GRCh38#69193466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87157057-C-A

69193466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87157057-C-T

69193500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87157023-T-C

69194282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87156758-C-T

http://identifiers.org/hco/2/GRCh38#69194440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87156618-A-C

69196703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87155722-G-T

69196747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87155679-A-G

69196966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87155521-G-A

69197454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87155110-C-T

69197502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87155069-G-T

69197762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87154837-G-A

69198198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87154414-T-C

69199089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87153986-G-A

69199462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87153632-G-A

69199700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87153422-G-A

69199737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87153416-C-T

69199982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87153203-G-A

69200289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87152911-A-G

69200294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87152906-C-T

69200406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87152771-G-A

69200406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87152771-G-C

69200406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87152771-G-T

69200665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87152560-G-T

69200710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87152515-C-T

69200731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87152494-C-G

69201164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87152119-G-A

69201364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151987-G-A

69201364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151987-G-T

69201492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151921-T-C

69201664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151795-C-G

69202147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151431-G-A

69202201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151398-G-A

http://identifiers.org/hco/2/GRCh38#69202207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87151392-A-C

69202630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87151104-G-A

69203151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87150553-A-G

69203321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87150372-G-T

69203638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87150063-C-T

69203700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87149967-C-G

69203713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87149954-A-T

69203736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87149930-T-G

http://identifiers.org/hco/2/GRCh38#69203829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87149808-C-A

69203960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87149675-G-A

http://identifiers.org/hco/2/GRCh38#69204197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87149395-A-C

http://identifiers.org/hco/2/GRCh38#69204402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87149210-C-A

69204980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87148659-T-C

69205108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87148546-C-T

69205679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87148060-C-T

69205807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147993-T-C

69205808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147992-G-A

69206029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147826-T-C

69206096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147763-G-A

69206370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147543-A-G

69206429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147507-G-A

69206471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147467-T-C

69206518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147418-C-T

69206729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147244-A-G

69206741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147232-C-G

69206842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87147118-A-G

69207067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87146921-A-G

69207302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87146697-T-C

69207355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87146642-C-G

69208278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87146187-C-T

69209209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87145620-A-G

http://identifiers.org/hco/2/GRCh38#69209318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87145525-C-A

69209318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87145525-C-T

69209352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87145491-T-C

69209480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87145369-C-T

69209862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144998-T-C

69209946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144945-C-T

69209958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144933-G-A

69210211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144709-C-G

69211117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144203-G-A

http://identifiers.org/hco/2/GRCh38#69211172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87144153-A-C

69211197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87144130-G-A

69211371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143956-C-T

69211398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143929-G-C

69211430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143897-A-T

69211465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143859-A-T

69211619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143714-A-T

http://identifiers.org/hco/2/GRCh38#69211636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87143697-C-A

69211636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143697-C-G

69211768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143581-T-C

69212264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143255-G-A

69212290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87143233-A-G

69213306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142741-C-T

69213394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142650-C-T

http://identifiers.org/hco/2/GRCh38#69213395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87142649-A-C

69213448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142596-T-C

69213604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142442-C-T

69213782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142267-T-A

69213908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142143-G-A

69213943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142124-G-A

69213943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142124-G-T

69213958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87142109-G-A

69214488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87141396-T-C

http://identifiers.org/hco/2/GRCh38#69214568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87141320-A-C

http://identifiers.org/hco/2/GRCh38#69214647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87141257-C-A

69214874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87141090-C-G

69215156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87140891-A-G

69215289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87140772-A-G

69215317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87140745-A-G

69215425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87140647-G-C

69215796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87140121-T-C

69216263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87139638-A-G

69216374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87139557-C-T

69217124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87138877-C-G

69217129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138872-G-A

69217388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138645-T-C

69217423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138614-A-G

69217726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138398-G-A

69217749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138376-G-A

69217749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138376-G-T

69217767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138358-C-G

69217767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138358-C-T

69217906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138232-G-A

69217936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138203-G-A

69217939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138200-C-T

69218027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138115-C-T

69218172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87138010-G-A

69218402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137820-A-G

69218424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137798-T-C

69218625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137662-A-G

69218900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137453-A-G

69218957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137412-C-G

69219083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137296-G-A

69219260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137129-T-C

69219265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137124-G-T

69219271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137118-G-A

69219274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137116-T-C

69219380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137046-G-A

69219380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87137046-G-T

69220058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87135796-G-A

http://identifiers.org/hco/2/GRCh38#69220097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87135759-C-A

69220393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87135513-C-T

69220546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87135368-T-C

69220589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87135322-A-G

69220597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87135314-C-T

69220767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134941-G-C

69220969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134772-A-G

69221073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134192-G-C

69221183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134107-A-G

69221289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134023-C-G

69221289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87134023-C-T

69221666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87133630-C-T

69221771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87133558-G-T

69221915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87133414-G-T

69222039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87133310-T-C

69222218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87133187-T-C

69222455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87132994-C-T

69222594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87132851-A-G

69222825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87132670-A-G

http://identifiers.org/hco/2/GRCh38#69223189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87132147-A-C

69223207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87132129-G-A

69223477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131879-G-A

69223566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131814-T-G

69223569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131811-G-A

69223569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131811-G-T

69223759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131640-T-G

69223795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131608-C-G

69223828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131596-G-A

69223845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131579-C-T

69224028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87131397-A-G

69225032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130557-T-C

69225155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130467-C-T

69225157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130465-C-T

69225170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130452-C-T

69225201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130420-A-G

69225324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130304-A-G

69225664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87130018-A-T

69225825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129869-T-C

69225924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129775-A-G

69226142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129629-G-A

http://identifiers.org/hco/2/GRCh38#69226155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87129612-C-A

69226407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129400-T-G

69226496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129312-G-A

69226504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129304-G-A

69226559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87129269-A-G

http://identifiers.org/hco/2/GRCh38#69226717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87129003-C-A

http://identifiers.org/hco/2/GRCh38#69226723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87128997-C-A

69227026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128661-C-T

69227361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128396-T-C

69227428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128329-C-G

69227428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128329-C-T

69227450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128308-C-G

69227450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87128308-C-T

http://identifiers.org/hco/2/GRCh38#69227481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87128277-A-C

http://identifiers.org/hco/2/GRCh38#69229175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87127705-A-C

69229314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87127565-C-G

69230040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87126829-C-T

69230079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87126788-A-G

69230525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125798-G-A

69230568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125753-T-C

69230599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125721-T-C

69230613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125707-A-G

69230731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125606-A-G

http://identifiers.org/hco/2/GRCh38#69230733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87125604-C-A

69231363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87125179-G-T

69231649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87124926-G-A

69232220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87124237-T-C

http://identifiers.org/hco/2/GRCh38#69232467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87124049-C-A

69232475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87124044-G-A

http://identifiers.org/hco/2/GRCh38#69232479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87124040-C-A

69232713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87123824-G-A

69232713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87123824-G-T

http://identifiers.org/hco/2/GRCh38#69232794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87123743-A-C

69232860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87123678-C-T

69236971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87121135-C-T

69237066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87121027-C-T

69237232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120872-C-T

69237671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120509-T-C

69237866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120378-G-A

69237989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120266-G-A

69238014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120249-G-T

69238123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120175-G-T

69238182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120121-G-A

69238186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120117-A-G

69238187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87120116-T-C

69238606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87119737-T-C

69238861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87119485-C-T

http://identifiers.org/hco/2/GRCh38#69239169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87119179-A-C

69239169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87119179-A-G

69239244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87119100-T-C

69239521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87119073-G-A

69239649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118998-G-A

http://identifiers.org/hco/2/GRCh38#69239687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87118962-C-A

69239949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118766-C-T

69240118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118521-T-G

69240161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118481-G-T

69240591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118154-G-A

69240600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118145-T-C

69240627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87118125-G-T

69240884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87117748-T-C

69240948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87117663-C-T

69240993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87117623-C-T

69241152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87117398-G-C

69241531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87117007-G-A

69241560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116983-C-T

69241561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116982-T-C

69241604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116898-C-G

69241626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116852-C-G

69241626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116852-C-T

69241850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116650-G-A

http://identifiers.org/hco/2/GRCh38#69242605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87116369-C-A

69242606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116368-C-T

69243055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87116001-G-T

69243235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115834-A-T

http://identifiers.org/hco/2/GRCh38#69243277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87115788-C-A

69243277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115788-C-T

69243550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115539-C-T

69243612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115453-C-T

69243720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115311-A-T

69243764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115267-C-T

69243859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87115167-C-T

69244897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87114657-C-G

69244954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87114602-A-G

69245051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87114501-A-G

69245063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87114476-T-C

69245146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: intron variant
orthologous variants: 87114409-G-A

69245288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114272-G-A

http://identifiers.org/hco/2/GRCh38#69245333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87114227-C-A

69245333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114227-C-T

http://identifiers.org/hco/2/GRCh38#69245363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87114197-C-A

69245363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114197-C-T

69245393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114167-T-A

69245393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114167-T-C

69245393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114167-T-G

http://identifiers.org/hco/2/GRCh38#69245396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87114164-C-A

69245396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: missense variant
orthologous variants: 87114164-C-T

http://identifiers.org/hco/2/GRCh38#69245576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87113983-C-A

69245577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113982-C-T

http://identifiers.org/hco/2/GRCh38#69245735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87113846-C-A

69245770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113810-G-C

69245770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113810-G-T

69245790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113790-A-G

69245790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113790-A-T

http://identifiers.org/hco/2/GRCh38#69245887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87113721-C-A

http://identifiers.org/hco/2/GRCh38#69245891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87113717-C-A

69245891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113717-C-G

69245891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113717-C-T

69245900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113708-T-C

69245903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113705-G-A

69245903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113705-G-C

69245903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113705-G-T

69245915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113693-A-G

69245917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113691-G-A

69246019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113623-T-C

69246092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113558-C-T

69246153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113514-T-A

69246214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113453-G-A

69246214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113453-G-T

69246225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113445-T-G

69246264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113424-G-A

69246264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113424-G-T

69246312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113377-A-T

http://identifiers.org/hco/2/GRCh38#69246556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87113213-A-C

69246556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113213-A-G

69246646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87113108-A-G

http://identifiers.org/hco/2/GRCh38#69246900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87112874-C-A

69247375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112459-C-T

http://identifiers.org/hco/2/GRCh38#69247400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87112434-C-A

69247400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112434-C-T

http://identifiers.org/hco/2/GRCh38#69247418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87112416-C-A

69247458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112385-A-G

69247459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112384-G-T

69247495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112372-T-C

69247796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112094-G-T

69247866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112033-G-A

69247866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87112033-G-T

69247948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111955-G-T

69248029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111883-A-G

69248074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111841-G-A

69248074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111841-G-T

http://identifiers.org/hco/2/GRCh38#69248185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87111735-C-A

69248557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111367-A-G

69248630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111291-T-C

69248811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111152-T-A

69248811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87111152-T-G

http://identifiers.org/hco/2/GRCh38#69248927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87111067-C-A

69249147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21014
most severe consequence: 3 prime UTR variant
orthologous variants: 87110859-A-G