22713373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 70297197-G-T

22713407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70297165-G-A

22713407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70297165-G-C

22713407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 70297165-G-T

22713638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296938-G-A

22713661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296924-G-A

22713661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296924-G-T

22713666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296919-G-A

22713666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296919-G-T

22713766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296825-G-C

22714036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296561-C-T

22714037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296560-C-G

22714271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296341-A-G

22714546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70296068-T-C

http://identifiers.org/hco/8/GRCh38#22714731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70295884-C-A

22714731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70295884-C-T

22714790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70295833-A-G

22715632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294882-G-A

22715632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294882-G-T

http://identifiers.org/hco/8/GRCh38#22715712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70294788-C-A

22715923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294556-G-A

22716016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70294498-C-G

22716016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70294498-C-T

22716222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294383-T-G

22716346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294254-T-C

http://identifiers.org/hco/8/GRCh38#22716446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70294170-C-A

22716502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70294107-G-A

http://identifiers.org/hco/8/GRCh38#22716746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70293905-C-A

22716941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70293772-A-G

22717606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70293504-G-A

22717725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70293410-T-A

22717726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70293409-C-G

22718484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292756-G-A

22718543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292703-T-C

22718799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292384-G-A

22718799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70292384-G-T

22719620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291533-G-C

22719743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291441-G-A

22719743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70291441-G-T

http://identifiers.org/hco/8/GRCh38#22720796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70290368-A-C

22720848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290322-G-C

22720915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290262-C-T

22721034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290166-G-T

22721224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70290004-G-C

22721300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289933-C-T

http://identifiers.org/hco/8/GRCh38#22721655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70289467-C-A

22721989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289151-G-A

22721989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289151-G-C

22722041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70289114-G-A

22722165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70288984-C-T

22722567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287751-A-G

http://identifiers.org/hco/8/GRCh38#22723323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70287351-C-A

22723323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287351-C-T

22723399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287273-T-C

22723572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287060-C-G

22723572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287060-C-T

22723628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70287008-G-A

22723638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286998-A-G

22723711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286921-G-A

22723711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286921-G-T

22723859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286758-C-G

22723928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286690-T-C

22724357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286338-G-A

http://identifiers.org/hco/8/GRCh38#22724717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70286047-C-A

http://identifiers.org/hco/8/GRCh38#22724744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70286019-A-C

22724744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286019-A-G

22724744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70286019-A-T

22724963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70285799-G-T

http://identifiers.org/hco/8/GRCh38#22725010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70285731-C-A

22725010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285731-C-T

22725242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285515-C-T

22725329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285422-T-G

http://identifiers.org/hco/8/GRCh38#22725339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70285412-A-C

22725436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285312-G-A

22725456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285292-T-A

22725581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285172-G-A

22725581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285172-G-T

http://identifiers.org/hco/8/GRCh38#22725592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70285161-C-A

22725730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70285026-G-A

22726037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284683-G-A

22726037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284683-G-T

22726043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284677-G-A

22726323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284415-C-T

22726357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284406-C-T

22726511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284278-T-C

22726534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284243-G-C

22726597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284173-C-T

22726600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284170-T-G

http://identifiers.org/hco/8/GRCh38#22726642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70284106-A-C

22726643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284105-T-C

22726717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284037-G-C

http://identifiers.org/hco/8/GRCh38#22726727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70284029-C-A

22726727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70284029-C-T

22726949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283770-A-G

22727054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283489-G-A

22727054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283489-G-T

http://identifiers.org/hco/8/GRCh38#22727104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70283439-A-C

22727104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283439-A-G

22727135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283409-T-C

22727160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283384-T-C

22727160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283384-T-G

22727165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283379-T-C

22727273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283247-C-T

http://identifiers.org/hco/8/GRCh38#22727276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70283244-C-A

22727276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283244-C-G

22727276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283244-C-T

22727443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283098-G-A

22727546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70283007-G-A

22728468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282212-T-G

22728517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282179-C-G

22728517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282179-C-T

22728546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282147-T-G

22728845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70282017-G-A

22729101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281955-G-A

22729560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281458-A-T

22729798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70281246-A-G

22730126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280906-G-T

22730192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280750-G-T

22730229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280713-T-C

22730229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280713-T-G

http://identifiers.org/hco/8/GRCh38#22730234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70280708-C-A

22730234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280708-C-T

22732206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70280014-G-A

22732254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279978-G-A

22732913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279611-C-T

22732975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279558-G-C

22733031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279494-C-T

22733037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279488-G-T

22733194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279424-C-T

22733446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279234-T-C

22733524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70279155-A-G

22733823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70278853-G-C

http://identifiers.org/hco/8/GRCh38#22733839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70278840-A-C

http://identifiers.org/hco/8/GRCh38#22734535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70278093-C-A

22734539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70278089-G-C

22734782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70277942-G-T

22735070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70277741-C-G

22735320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70277537-G-A

22735347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70277510-A-G

22735493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70277018-T-G

22735546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276970-T-C

http://identifiers.org/hco/8/GRCh38#22737534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70276406-C-A

22737534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276406-C-G

22737541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276399-C-T

22737683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276260-G-A

22737693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276250-G-A

22737964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70276005-G-A

22738346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275582-G-A

22738478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275463-G-A

22738478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275463-G-T

22738556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275353-G-A

22738778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70275136-C-T

22738834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274493-C-T

22739149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70274208-G-A

22739448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70273916-T-G

22739514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70273816-C-G

http://identifiers.org/hco/8/GRCh38#22739766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70273616-C-A

22739766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273616-C-T

22739864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273520-T-C

22739867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273517-C-T

22739950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273435-T-G

22740004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273376-C-G

22740161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273139-A-G

22740179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70273121-A-G

22740396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272940-C-G

http://identifiers.org/hco/8/GRCh38#22740422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70272913-C-A

22740583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272568-G-T

22740595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272552-G-A

22740680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272474-T-C

22740680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272474-T-G

22740698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272456-G-A

22740718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272439-G-A

22740719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272438-G-A

22740719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272438-G-T

22740979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272205-G-A

22741178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70272016-T-A

22741238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271955-T-C

22741625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271604-G-C

22741667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271586-G-A

22741908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271371-C-G

22741908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271371-C-T

22742227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271132-C-G

http://identifiers.org/hco/8/GRCh38#22742238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70271120-C-A

22742238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70271120-C-T

22742765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270644-G-A

22742847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270572-T-C

22742853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270566-G-A

22743034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270384-G-T

22743150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270305-T-G

22743261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270252-G-A

22743262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270251-C-T

22743441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70270080-A-G

22743554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70269942-G-A

22743577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269916-G-A

22743577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269916-G-T

22743600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269893-C-T

22744242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70269097-G-T

22744339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70269021-T-A

22744451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268908-C-T

22744512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268845-A-G

22744855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268665-T-A

http://identifiers.org/hco/8/GRCh38#22744876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70268648-C-A

22744876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268648-C-T

22745506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70268114-T-C

http://identifiers.org/hco/8/GRCh38#22745617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70268023-C-A

22745617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70268023-C-G

22745617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70268023-C-T

22745650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70268000-G-A

22745650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70268000-G-T

http://identifiers.org/hco/8/GRCh38#22745718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70267938-C-A

22745718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267938-C-T

22745719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267937-C-T

22745783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267903-G-C

22745783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267903-G-T

22745814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267882-C-T

22745871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267809-A-G

22746023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267653-T-C

22746047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70267632-C-T

http://identifiers.org/hco/8/GRCh38#22746527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

22746736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

22746746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

22746749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

22747648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70266795-T-A

22747648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70266795-T-C

22748010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70266434-G-T

22748484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70265947-G-A

22748498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70265933-A-G

http://identifiers.org/hco/8/GRCh38#22748836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70265593-C-A

22749111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70265336-G-T

22749114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70265333-T-C

22749652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70264842-C-T

22751583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70263629-T-G

http://identifiers.org/hco/8/GRCh38#22752434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70262891-C-A

22752528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70262794-A-G

22752772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70262568-T-C

22753018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70262342-T-C

http://identifiers.org/hco/8/GRCh38#22753335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70262026-A-C

22753696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70261038-G-A

22754599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260386-G-A

22754599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260386-G-C

22754599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260386-G-T

22754717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260264-C-T

22754720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70260261-G-A

22755218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70259791-C-G

22755224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70259785-T-G

22755675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70259662-T-G

22755805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259535-G-A

22755805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259535-G-T

22755869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259471-G-T

22755914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70259429-A-G

22756415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70258858-A-G

22756535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70258705-C-T

22756551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70258695-G-A

22756787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70258470-G-A

22756992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258258-A-G

http://identifiers.org/hco/8/GRCh38#22757005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70258245-C-A

http://identifiers.org/hco/8/GRCh38#22757159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70258096-C-A

22757181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258075-G-T

22757199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258057-A-T

22757208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258048-A-G

22757238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70258018-C-T

22757260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257992-C-T

22757570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257678-T-C

22757661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257600-G-T

22757703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257548-A-T

22757728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257508-G-A

http://identifiers.org/hco/8/GRCh38#22757799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70257437-C-A

22757799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257437-C-T

22757863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257400-G-A

22757863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257400-G-C

22757881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257382-T-C

22757901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257370-T-C

22757929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257367-T-C

http://identifiers.org/hco/8/GRCh38#22757980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70257319-C-A

http://identifiers.org/hco/8/GRCh38#22758045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70257267-C-A

http://identifiers.org/hco/8/GRCh38#22758150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70257172-C-A

22758155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257148-G-T

http://identifiers.org/hco/8/GRCh38#22758156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70257147-C-A

22758156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70257147-C-G

22758267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70256913-T-C

22758304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70256832-C-G

22758304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70256832-C-T

http://identifiers.org/hco/8/GRCh38#22758330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70256807-C-A

22758341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70256798-G-A

22760520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70255602-G-A

22761177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70255011-G-C

http://identifiers.org/hco/8/GRCh38#22761267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70254938-C-A

22761267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70254938-C-T

22761353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70254870-G-A

22761443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70254779-G-A

http://identifiers.org/hco/8/GRCh38#22762005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70254199-A-C

22762170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70254005-C-T

22762382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253792-C-G

22762382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253792-C-T

22762428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253732-C-T

22762496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253681-G-A

22762496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253681-G-T

22762566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70253616-C-T

22763507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252898-A-G

22763745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70252681-C-T

http://identifiers.org/hco/8/GRCh38#22765443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70250173-C-A

22765444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70250172-C-G

22765676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249947-G-A

22765747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249873-G-A

22766153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249297-T-A

22766225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249224-G-A

22766284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249168-C-G

22766321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70249130-G-A

22766525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248925-A-T

22766936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248547-C-T

22766966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248517-G-T

22767006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248478-T-C

22767163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248318-G-T

22767170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70248311-G-A

22768104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70247288-C-T

22768250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70247136-C-G

22768336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70247022-T-G

http://identifiers.org/hco/8/GRCh38#22768476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70246910-C-A

22768476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246910-C-T

22768763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246638-G-A

22768763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246638-G-T

22769304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246223-C-T

22769452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70246019-C-T

22769520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245950-T-C

22770103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245256-A-G

22770114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245245-G-A

22770165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245183-G-C

22770199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70245150-G-T

22770301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244397-A-G

22770399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244322-C-T

22770510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244187-G-C

22770530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70244167-T-C

22770797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243414-A-G

22771076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243168-G-A

22771116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243128-A-G

22771140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70243104-T-C

22772343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242751-G-A

22772350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242744-A-G

22772368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242726-C-T

22772496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242596-T-C

22772497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70242595-T-C

22773353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70241552-A-T

22773369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70241536-A-T

22773437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70241485-G-C

22773810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70241222-G-A

22774088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240958-G-A

22774088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240958-G-T

22774304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240717-G-A

22774304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240717-G-T

22774501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240520-C-T

22774540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240479-A-G

22774816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240192-T-C

22774859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240148-C-G

22774969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240048-G-A

22774969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70240048-G-C

22775023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239998-C-G

22775023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239998-C-T

http://identifiers.org/hco/8/GRCh38#22775126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70239888-C-A

22775126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239888-C-G

22775185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239825-C-T

http://identifiers.org/hco/8/GRCh38#22775896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70239116-A-C

22775947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70239065-G-A

http://identifiers.org/hco/8/GRCh38#22776171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70238901-A-C

22776171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238901-A-G

22776275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238821-T-C

22776558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238550-C-T

22776706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238431-C-T

22776783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238344-G-A

22776783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238344-G-C

22776783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238344-G-T

22776787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238340-A-G

22776810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238317-C-T

22776840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238287-C-T

22776923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238216-A-G

22776960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70238179-C-T

22777407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236653-G-A

22777426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236608-G-C

22777638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236392-G-A

22777718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236327-C-T

22777722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236323-C-G

22777831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70236196-G-A

22778169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235893-C-G

22778171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235891-T-C

22778236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235825-G-A

22778336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235727-G-A

22778669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235538-G-C

22778767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235429-C-T

22778842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70235361-T-C

http://identifiers.org/hco/8/GRCh38#22778860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70235343-A-C

22779208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234959-G-A

22779208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234959-G-C

22779220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234947-C-T

22779381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234784-G-A

22779446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70234722-G-A

http://identifiers.org/hco/8/GRCh38#22779708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70234459-A-C

22780407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233691-G-T

http://identifiers.org/hco/8/GRCh38#22780423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70233675-C-A

22780511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233397-A-T

22780670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70233233-C-T

22781166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232787-G-A

22781304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232660-G-C

22781304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232660-G-T

22781838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232156-C-T

http://identifiers.org/hco/8/GRCh38#22781959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70232039-C-A

22781959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232039-C-T

http://identifiers.org/hco/8/GRCh38#22781980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70232020-C-A

22781987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70232013-T-G

22782833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230765-T-C

22783087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230591-C-T

22783446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70230249-G-A

22784456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229608-A-G

22784600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229488-G-A

22784600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229488-G-T

22784936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70229138-G-A

22785209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70228908-T-A

22785283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70228792-T-C

22785628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70228521-G-A

22785956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70228187-G-A

22785956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70228187-G-T

22786051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70228089-C-T

22787264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227727-T-G

22787521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227475-T-A

22787736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227331-C-T

22787756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227323-G-A

22787937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227158-G-A

22787937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227158-G-T

22787942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227153-G-A

22787942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227153-G-T

22787975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227120-G-A

22787996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227099-G-A

22787996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70227099-G-C

22788569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226565-G-A

22788569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226565-G-C

22788569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226565-G-T

22788595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226540-T-C

22788595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226540-T-G

22788730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226427-G-A

22788809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70226350-C-T

22789295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225826-T-G

22789455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225676-C-T

22789524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225612-G-A

22789708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70225446-C-G

22790846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70223465-A-G

22791062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70223246-G-C

22791230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70223084-C-G

22791230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70223084-C-T

22791556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70222731-G-A

22791693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70222584-G-A

22792458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221804-C-T

22792487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221775-A-T

22792617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221663-C-T

22792740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221581-C-T

22793168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70221147-A-G

22793481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220636-A-G

22793872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70220088-G-A

http://identifiers.org/hco/8/GRCh38#22793874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70220086-C-A

22793992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219976-T-C

22794041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219931-G-T

22794105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70219866-T-A

http://identifiers.org/hco/8/GRCh38#22794277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70219602-C-A

22795699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218685-G-T

22796346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70218049-G-T

22796426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217951-G-A

22796552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217831-A-T

http://identifiers.org/hco/8/GRCh38#22796640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70217744-A-C

22796640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217744-A-G

22797461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217627-G-A

22797531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217560-C-T

22797656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217441-G-A

http://identifiers.org/hco/8/GRCh38#22797888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70217276-C-A

22798074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70217091-G-A

22798405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216762-A-G

http://identifiers.org/hco/8/GRCh38#22798434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70216734-C-A

22798434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216734-C-T

http://identifiers.org/hco/8/GRCh38#22798447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70216721-C-A

22798474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216693-G-A

22798474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216693-G-T

http://identifiers.org/hco/8/GRCh38#22798483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70216684-C-A

22798483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216684-C-G

22798483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216684-C-T

http://identifiers.org/hco/8/GRCh38#22798512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70216654-C-A

22798512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70216654-C-T

22798562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70216604-G-A

22798562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70216604-G-T

22798679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70216472-T-C

22799267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70215961-G-A

22799455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70215791-G-A

22800209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70215617-G-A

22800267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70215557-G-T

22800809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214790-A-G

22800919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214731-C-T

22800975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214690-G-A

22800980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214685-C-T

22801006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214659-C-T

22801043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214620-T-A

22801348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214325-A-T

22801408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214267-T-C

22801591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214085-T-C

22801663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214010-G-C

22801663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70214010-G-T

22801702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70213969-T-C

22802289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70213288-A-G

22802318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70213259-C-T

22802428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70213151-C-G

22802487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70213072-G-C

22802846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70212695-T-C

22802953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70212598-C-T

22803051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70212503-C-T

22804727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70211149-G-T

22805818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70210764-T-C

22805876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70210713-T-A

22805913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70210662-G-T

22806301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70210249-T-C

22806326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70210225-G-C

22810483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70208253-C-T

22810688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207962-G-A

22810703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207947-T-A

22810707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207943-T-A

22810709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207941-T-A

22810711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207939-T-A

22810711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207939-T-C

22810713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207937-T-A

22810715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207935-A-T

22810894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207754-G-T

22811047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70207623-G-T

22811567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70207082-C-T

http://identifiers.org/hco/8/GRCh38#22812690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70206593-C-A

22813130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70205827-C-T

22813690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70205280-A-G

22813816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204978-T-C

22813971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204862-G-C

22814489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204421-A-G

22814498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204412-G-A

http://identifiers.org/hco/8/GRCh38#22814509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70204401-A-C

22814637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204272-G-C

22814891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204045-G-A

22814891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204045-G-C

22814894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70204042-G-T

22814944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70203997-G-T

22814948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70203993-C-T

22815080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70203865-G-T

22815176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70203773-A-G

22815298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70203643-T-C

22816832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70202070-G-A

22816874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70202028-T-C

22817224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70201365-C-T

http://identifiers.org/hco/8/GRCh38#22817540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70201109-C-A

22817540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70201109-C-T

22817579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70201058-T-G

22817582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70201055-T-C

22817584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70201053-A-G

22817768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70200854-T-G

22817812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70200805-C-T

22818085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70200535-A-T

22818127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70200498-G-T

22818830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70199890-G-A

22818877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70199843-G-T

22818921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70199802-T-C

22818934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70199789-T-A

22820190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70198231-G-A

22820546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197992-G-A

22820546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197992-G-C

22820596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197941-A-G

22820598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197939-C-T

22820637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197918-T-C

http://identifiers.org/hco/8/GRCh38#22822335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70197310-A-C

22822572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197066-T-C

22822614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70197018-A-G

22827046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190894-T-C

22827211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190758-A-T

http://identifiers.org/hco/8/GRCh38#22827411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70190350-C-A

22827485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190276-G-A

22827508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190253-T-C

22827618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190129-A-G

22827618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190129-A-T

http://identifiers.org/hco/8/GRCh38#22827633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70190118-C-A

http://identifiers.org/hco/8/GRCh38#22827693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70190064-C-A

22827693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70190064-C-T

22832727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70188764-G-C

22832728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70188763-G-T

22833299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70187616-C-T

22833518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70187363-G-A

22833518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70187363-G-C

22833721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70187175-G-A

22833938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186966-G-A

22833988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186918-A-G

22834140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186773-A-G

22834147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70186766-C-T

22834748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70185519-T-G

22835305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70184783-T-C

22835321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70184768-T-A

22838706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70181723-T-C

22838707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70181722-G-A

22839113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70181315-G-C

22839346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70181081-T-C

22839378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70181050-C-T

22839436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180992-G-A

22839455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180973-T-C

22839813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180634-T-A

22839846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180603-C-G

22839846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180603-C-T

22839852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180597-G-A

22839852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180597-G-C

22839852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180597-G-T

22839860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180589-C-G

22839876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180573-G-A

22839973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180503-T-C

22840056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70180422-A-T

22840626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70179826-C-T

22840817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70178610-C-T

22841391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70178011-A-G

22841637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177808-G-A

22841689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177768-G-T

22841813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177676-A-G

22841939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177577-C-G

22842008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70177520-G-A

22842187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70177371-T-C

22842508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70177059-G-C

22843574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70176442-C-T

22845100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174979-C-T

22845641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70174768-T-G

22846153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173697-G-A

22846228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173640-G-T

http://identifiers.org/hco/8/GRCh38#22846251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70173617-A-C

22846337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173531-G-A

22846343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173525-G-A

22846348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173520-A-G

22846470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173398-A-G

22846470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173398-A-T

22846498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70173370-T-C

22846583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70173302-A-G

22846860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70173020-G-A

http://identifiers.org/hco/8/GRCh38#22847278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70172542-C-A

22847593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172290-T-C

22847655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172218-T-C

22847694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172179-C-G

22847694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172179-C-T

22847703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172158-A-G

22847711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172153-G-A

22847711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70172153-G-C

22848447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70171388-G-A

22848502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70171322-A-T

22848551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70171267-G-A

22848574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70171244-G-A

22849300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70170350-T-C

http://identifiers.org/hco/8/GRCh38#22850158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70169077-C-A

22850555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70168555-G-A

22850556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70168554-C-T

22850845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70168190-T-C

22850846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70168189-T-G

22850847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70168188-G-A

22851101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167902-C-G

http://identifiers.org/hco/8/GRCh38#22851134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70167874-C-A

22851134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167874-C-G

22851134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167874-C-T

22851362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167671-G-A

22851362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167671-G-T

22851364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70167669-T-G

22851650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70166639-G-A

22851650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70166639-G-C

22852866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70165415-G-A

22853391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70164869-T-C

22853580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70164703-G-C

22853665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70164619-C-T

http://identifiers.org/hco/8/GRCh38#22853869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70164413-A-C

22853885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70164397-T-C

22854028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163810-A-G

22854044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163794-C-G

22854053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163785-C-T

22854083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163757-G-T

22854157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163654-C-T

22854794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70163054-C-T

22854958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162829-G-A

22854958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162829-G-C

22854958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162829-G-T

http://identifiers.org/hco/8/GRCh38#22854961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70162826-C-A

22854961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162826-C-G

22854962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162825-A-G

22854962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162825-A-T

22854967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162820-T-A

22854967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162820-T-G

22854969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162818-T-G

22854992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162795-G-A

22854992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162795-G-T

22854995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162792-T-A

22854995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162792-T-G

22854996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162791-G-A

22854996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162791-G-T

http://identifiers.org/hco/8/GRCh38#22854998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70162789-A-C

22854998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162789-A-T

22855045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162707-T-A

22855045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162707-T-C

22855045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162707-T-G

http://identifiers.org/hco/8/GRCh38#22855384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70162432-C-A

22855384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70162432-C-T

22857937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70159271-G-T

22858210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158998-G-A

22858371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70158836-A-G

22858454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70157345-C-T

22859121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156992-A-G

22859199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156924-A-G

22859270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156861-A-G

22859637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156597-C-G

22859685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156549-C-T

22859731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156503-A-G

22859794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70156453-C-T

http://identifiers.org/hco/8/GRCh38#22863559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70150966-C-A

22863559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150966-C-G

22863891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150624-T-C

22863917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150600-C-T

22864025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150497-A-G

22864062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150446-C-T

22864063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150445-G-A

22864312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150240-T-G

22864527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150066-G-A

22864527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70150066-G-T

22864711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70149885-T-A

22864881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70149714-G-A

22864881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70149714-G-T

http://identifiers.org/hco/8/GRCh38#22864992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70149562-A-C

22865091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70149453-T-C

22865297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149265-C-T

22865300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149262-C-T

22865423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149174-G-A

22865423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149174-G-T

22865549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149031-G-T

http://identifiers.org/hco/8/GRCh38#22865553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70149027-C-A

22865553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70149027-C-T

22865636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148941-C-T

22865696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148873-G-A

22865696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148873-G-T

22865820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148760-C-T

22866127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148569-G-A

22866177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148532-T-C

22866315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148409-G-A

22866589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148159-C-G

22866620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70148128-A-G

22867006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70147809-T-G

22867653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70147122-C-T

22867824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146977-C-G

22867978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146823-T-C

22868143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146661-A-G

22868192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146624-C-T

22868295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146453-T-C

22868306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146438-G-A

22868441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70146300-G-A

22869912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143769-C-T

22870169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143581-T-C

22870287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143479-C-T

22870406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143371-T-C

22870581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143211-G-A

22870594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70143204-G-A

22871418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70142245-A-G

22872355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70141835-A-G

22873796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139791-G-A

http://identifiers.org/hco/8/GRCh38#22874019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70139610-C-A

22874280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70139374-T-C

22876475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70137226-G-C

22876593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70137136-C-T

22876832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136450-C-T

22877033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70136233-A-G

22877757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70135362-G-A

22877760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70135359-G-A

22877760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70135359-G-C

22877866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70135242-G-A

http://identifiers.org/hco/8/GRCh38#22878430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70134823-C-A

22878911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70134332-A-G

22879523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70132408-A-G

22879541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70132390-A-G

22879581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70132358-C-T

22882051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128954-T-A

22882282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128699-T-C

22882669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70128411-T-G

22883104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70128027-C-T

22883676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70127095-T-C

22883898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70126871-A-G

22884041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126739-G-A

22884041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126739-G-C

22884041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126739-G-T

22884068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126712-A-G

http://identifiers.org/hco/8/GRCh38#22884194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70126601-C-A

22884516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126303-G-T

http://identifiers.org/hco/8/GRCh38#22884587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70126235-C-A

22884587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126235-C-T

22884671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126163-G-T

22884715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126128-T-C

22884716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126127-G-T

http://identifiers.org/hco/8/GRCh38#22884746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70126094-C-A

22884789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126049-G-A

22884789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70126049-G-T

22884889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125950-T-C

22884919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125934-T-C

22884934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125919-A-G

http://identifiers.org/hco/8/GRCh38#22884943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70125910-C-A

22884943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125910-C-T

http://identifiers.org/hco/8/GRCh38#22885005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70125877-A-C

22885064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125816-G-A

22885114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125768-T-C

22885115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125767-G-T

22885130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125744-A-G

22885180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70125698-C-T

22895693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70119027-T-C

22895949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70118775-G-T

22895952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70118772-T-C

http://identifiers.org/hco/8/GRCh38#22896490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70118287-C-A

22897395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70115268-A-G

22897419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70115245-G-T

22897581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70115083-G-A

22897886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70114632-T-C

22897898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70114620-G-A

22897898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70114620-G-T

22897985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70114528-G-C

22898551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70114298-C-T

http://identifiers.org/hco/8/GRCh38#22898703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70114152-C-A

22899265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70110804-G-A

22899432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70110628-T-C

22899439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70110611-G-A

22899651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70110420-T-C

22899934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70109967-G-A

http://identifiers.org/hco/8/GRCh38#22900016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70109810-C-A

22900050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70109776-T-G

http://identifiers.org/hco/8/GRCh38#22900060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70109767-A-C

22900208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70109619-C-T

http://identifiers.org/hco/8/GRCh38#22901087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70108770-A-C

22901087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70108770-A-G

22902474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70107086-T-C

22902521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70107042-T-C

22902551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70107012-C-T

22902722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70106889-G-A

22902722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70106889-G-C

22902994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70106737-G-A

22903188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70106553-C-T

22904246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70105632-C-G

22904246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70105632-C-T

22904510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70105392-G-A

22904510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70105392-G-T

22904894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104993-G-A

22904894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104993-G-C

22905064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104827-C-T

22905136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104759-C-T

22905141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104754-A-G

22905329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104348-G-A

22905329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104348-G-T

22905433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104277-G-A

22905433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70104277-G-T

22905752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70103992-C-T

22905972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70103811-A-G

22906103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70103700-C-T

22906231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70103588-G-A

22906661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70102875-A-T

22906682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70102854-T-A

22906685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70102851-C-T

22906937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70102617-A-G

22907577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70100307-G-A

22907646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70100237-G-A

22907856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70100040-A-G

22908691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099444-T-C

22908691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099444-T-G

22908861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099341-C-T

22908863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099339-T-A

22908863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099339-T-G

22908912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099276-C-T

http://identifiers.org/hco/8/GRCh38#22909027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70099184-C-A

22909045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70099166-G-A

22909101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70099097-T-C

22909200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70098995-A-T

22909238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70098964-T-C

22910683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097335-G-T

22910741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097279-A-G

22910750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097270-G-A

22910782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097241-C-G

22910836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097181-T-C

22911039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097022-G-A

22911039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70097022-G-T

22911142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096926-T-G

http://identifiers.org/hco/8/GRCh38#22911519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70096648-A-C

22911519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096648-A-G

22911581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096586-C-T

22911612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096555-A-G

22911628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096542-T-C

22911710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096473-A-G

22911710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096473-A-T

22911913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70096234-C-G

22912012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096155-G-A

22912012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096155-G-T

22912063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70096136-G-A

22912095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70096104-C-T

22912291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70095736-T-C

22912292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70095735-G-T

22913275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094890-A-G

22913308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094876-T-A

http://identifiers.org/hco/8/GRCh38#22913480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70094691-C-A

22913667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094567-G-A

22913705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094525-C-T

22913716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094517-G-A

22913753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094480-T-G

22913788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094444-T-C

22914564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094284-G-A

22914565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094283-C-T

22914582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70094264-C-T

22914958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70093889-C-T

22915081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70093781-C-T

22915096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70093766-C-T

http://identifiers.org/hco/8/GRCh38#22915408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70093582-A-C

22915408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70093582-A-G

http://identifiers.org/hco/8/GRCh38#22915483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70093514-C-A

22915497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70093500-G-A

22915644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70093378-C-T

22915718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70093286-T-C

22915718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70093286-T-G

22915896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70093108-C-T

22916210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70092791-A-G

22916268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70092733-T-C

22916407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70092563-G-C

22917081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70091694-T-G

22917134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70091647-G-A

22917134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70091647-G-C

22917234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70091559-G-A

22917303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70091482-C-T

22918076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70090931-A-G

22918450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70090637-G-A

22918732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70090433-T-A

22918823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70090335-C-T

22918885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70090271-G-A

22919107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70090095-A-G

22919212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089973-G-A

22919557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089735-C-T

22920070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089288-A-G

22920363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70089024-G-A

22920428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088956-T-A

22920524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70088856-T-C

22921385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087829-G-C

22921441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087775-G-C

22921489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087731-G-T

http://identifiers.org/hco/8/GRCh38#22921498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70087725-C-A

22921498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087725-C-T

22921651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087573-C-G

22921666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087558-G-A

22921876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70087095-A-G

22927430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70085262-C-G

22927437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70085255-G-A

22927437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70085255-G-T

http://identifiers.org/hco/8/GRCh38#22927522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70085165-C-A

22927522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70085165-C-T

22927893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70084758-A-G

http://identifiers.org/hco/8/GRCh38#22927952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70084698-C-A

22927952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084698-C-T

22928173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70084540-T-C

http://identifiers.org/hco/8/GRCh38#22928950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70083915-C-A

22928950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083915-C-G

22928950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083915-C-T

22929015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70083850-A-G

22940418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70078216-A-G

22940467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70078167-C-T

22941214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077742-T-C

22941215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077741-T-A

22941215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077741-T-C

22941237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077719-G-A

22941237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077719-G-T

22941238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70077718-A-G

22941348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70077628-G-A

22941348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70077628-G-T

22941377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70077607-G-A

22941377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70077607-G-T

22945314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70076188-A-G

22945476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70076051-T-G

22945822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70075765-G-T

22946120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70075450-G-A

http://identifiers.org/hco/8/GRCh38#22946234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70075337-A-C

22946409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70075262-A-G

22946417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70075254-G-C

22946973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074940-T-A

22947046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074864-G-A

22947079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074830-C-T

22947113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074796-G-C

22947113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074796-G-T

22947162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074758-G-A

22948115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074397-C-T

22948226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074287-G-A

http://identifiers.org/hco/8/GRCh38#22948254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70074259-C-A

22948254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron variant
orthologous variants: 70074259-C-G

22973866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068673-T-A

22974137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70068448-C-T

22974547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70067966-G-A

22974553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067960-G-C

http://identifiers.org/hco/8/GRCh38#22974682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70067834-A-C

22974903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067290-G-A

22974905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70067288-C-T

22975295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066986-C-G

22975445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70066832-G-T

22980956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70061594-A-T

22981411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70061249-C-T

22981514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70061149-G-C

http://identifiers.org/hco/8/GRCh38#22981901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70060854-C-A

http://identifiers.org/hco/8/GRCh38#22981955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70060795-C-A

22986914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70053917-G-C

22986936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053896-G-A

22986936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053896-G-C

22986970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053878-C-T

22987040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053810-A-G

22987240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053601-G-T

22987281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053575-G-A

22987317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053543-G-T

22987320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053540-A-G

22987373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70053497-G-A

22987373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70053497-G-T

22987383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70053487-A-G

http://identifiers.org/hco/8/GRCh38#22987423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70053453-C-A

22987423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053453-C-G

22987451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053425-G-T

22987452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053424-A-G

22987488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70053372-G-A

22987563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70053294-G-A

22987563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70053294-G-T

22987611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70053253-A-G

22988565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70052690-T-G

22988716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70052553-C-T

22988844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70052437-G-C

22988895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70052383-C-T

22989110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70052185-T-C

22989775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70051780-G-A

22989775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70051780-G-C

22989844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70051688-C-T

22989949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051563-T-C

22991944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70049719-A-T

22992080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70049598-T-C

22992254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70049410-C-T

22992883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70048780-G-A

22994419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047923-G-T

22994428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047914-G-C

22994428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047914-G-T

http://identifiers.org/hco/8/GRCh38#22994533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70047808-C-A

22994533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047808-C-G

22995402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047481-T-C

22995573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047316-G-C

22995604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70047295-G-A

http://identifiers.org/hco/8/GRCh38#22995857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70047073-C-A

22995857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70047073-C-T

22997942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044444-T-C

22998029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044364-T-A

22998059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70044334-C-G

22998127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70044277-G-C

22999161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70043423-C-G

22999161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70043423-C-T

22999211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70043392-G-A

http://identifiers.org/hco/8/GRCh38#22999347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043272-A-C

22999413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70043217-G-T

22999447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70043179-G-T

http://identifiers.org/hco/8/GRCh38#22999553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043085-C-A

22999553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043085-C-T

http://identifiers.org/hco/8/GRCh38#22999557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043081-C-A

22999557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043081-C-T

http://identifiers.org/hco/8/GRCh38#22999577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043060-C-A

22999577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043060-C-T

http://identifiers.org/hco/8/GRCh38#22999590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043047-C-A

22999590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043047-C-G

22999590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043047-C-T

22999591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043046-T-A

22999591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043046-T-C

22999596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043041-T-A

22999598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043039-T-C

http://identifiers.org/hco/8/GRCh38#22999606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043035-C-A

22999606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043035-C-G

22999606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043035-C-T

http://identifiers.org/hco/8/GRCh38#22999633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70043008-C-A

22999633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70043008-C-T

22999991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70042598-G-A

22999991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70042598-G-T