http://identifiers.org/hco/7/GRCh38#44748599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#6339109-C-A

44748599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6339109-C-G

44748599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 6339109-C-T

http://identifiers.org/hco/7/GRCh38#44748621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6339130-C-A

44748621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5 prime UTR variant
orthologous variants: 6339130-C-T

44748749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, undefined
orthologous variants: 6339267-G-A

44748749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, undefined
orthologous variants: 6339267-G-T

http://identifiers.org/hco/7/GRCh38#44748775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6339300-C-A

44748775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6339300-C-T

44748798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6339324-C-T

44749074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339581-T-C

44749074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339581-T-G

44749088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339593-T-C

44749088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339593-T-G

44749097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339602-G-A

44749097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6339602-G-T

44749417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6339842-G-A

http://identifiers.org/hco/7/GRCh38#44749659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6340096-A-C

http://identifiers.org/hco/7/GRCh38#44749701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6340133-C-A

44749752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340204-G-A

44749752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340204-G-C

44749865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 6340311-A-G

44749944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 6340391-G-A

http://identifiers.org/hco/7/GRCh38#44749967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6340409-C-A

44750235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340640-C-T

44750346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340726-C-T

44750420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340796-C-T

44750421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340797-G-A

44750441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6340946-C-T

44750773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6341440-T-C

44751028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 6341615-T-A

44751246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6341832-A-G

44751321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6341881-C-G

44751369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6341928-A-G

44751375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 6341934-T-C

44751414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6341963-G-C

44751529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6342027-T-G

44752450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6342541-T-G

44752490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6342581-G-C

44752647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6342707-G-A

http://identifiers.org/hco/7/GRCh38#44752656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6342715-C-A

44752833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6342877-A-G

44753171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6343171-A-T

44753234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6343209-G-A

44753234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6343209-G-T

44753320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6343248-C-T

44753751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6343562-G-C

44754381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344152-A-G

44754405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344164-T-C

44754446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344194-T-C

44754543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344288-G-T

44754684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344408-C-T

44754846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6344572-C-T

44755849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6345365-C-T

http://identifiers.org/hco/7/GRCh38#44756168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6345548-C-A

44756168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6345548-C-T

44756189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6345569-C-T

http://identifiers.org/hco/7/GRCh38#44756323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6345703-C-A

44756323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6345703-C-G

44756323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6345703-C-T

44756551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6345884-C-T

http://identifiers.org/hco/7/GRCh38#44756732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6346054-C-A

44756732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6346054-C-G

44756732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6346054-C-T

44757090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 6346375-C-T

44757093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 6346378-G-A

44757093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 6346378-G-C

http://identifiers.org/hco/7/GRCh38#44757163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6346448-C-A

44757163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346448-C-G

44757163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346448-C-T

44757189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346456-A-G

44757279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346594-G-A

44757350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346637-G-A

44757350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346637-G-C

44757365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346652-G-A

44757365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6346652-G-T

http://identifiers.org/hco/7/GRCh38#44757498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6346785-A-C

44757498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 6346785-A-G

44757549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 6346836-C-T

http://identifiers.org/hco/7/GRCh38#44757568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6346856-C-A

44757568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6346856-C-T

44757587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6346873-A-T

44757604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6346890-A-G

http://identifiers.org/hco/7/GRCh38#44757776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6346995-C-A

44757776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6346995-C-G

44757776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6346995-C-T

44757853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: synonymous variant
orthologous variants: 6347034-G-A

44758139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347319-T-A

44758139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347319-T-C

44759261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347489-G-A

44759261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347489-G-T

44759436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: synonymous variant
orthologous variants: 6347662-T-C

http://identifiers.org/hco/7/GRCh38#44759439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6347665-C-A

44759439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: synonymous variant
orthologous variants: 6347665-C-T

44759491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347716-G-T

http://identifiers.org/hco/7/GRCh38#44759523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6347743-C-A

44759523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron variant
orthologous variants: 6347743-C-G

44759652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, missense_variant
orthologous variants: 6347774-G-T

44759787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6347906-G-A

44759787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6347906-G-T

http://identifiers.org/hco/7/GRCh38#44759793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6347912-C-A

44759793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6347912-C-T

http://identifiers.org/hco/7/GRCh38#44759807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6347925-C-A

44759807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6347925-C-T

44759931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348048-A-G

http://identifiers.org/hco/7/GRCh38#44760057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6348170-A-C

44760068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348181-T-C

44760068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348181-T-G

44760232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348343-G-A

http://identifiers.org/hco/7/GRCh38#44760291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6348403-C-A

44760291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348403-C-T

44760310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348446-G-A

44760310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348446-G-T

44760330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348464-T-A

44760330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348464-T-C

44760330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348464-T-G

44760405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348535-G-A

44760405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6348535-G-C

44760541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348672-C-G

44760541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348672-C-T

http://identifiers.org/hco/7/GRCh38#44760548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6348679-C-A

44760548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6348679-C-G

44760583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348714-A-G

44760592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 6348723-T-C

44760732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348898-G-A

http://identifiers.org/hco/7/GRCh38#44761052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6349216-A-C

44761064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349228-T-C

44761229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349307-C-T

44761275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349354-A-G

44761275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349354-A-T

http://identifiers.org/hco/7/GRCh38#44761309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6349387-C-A

http://identifiers.org/hco/7/GRCh38#44761313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6349389-C-A

44761794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6349822-G-A

44761824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6349852-C-T

http://identifiers.org/hco/7/GRCh38#44761893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#6349921-C-A

44761893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6349921-C-T

44762319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350325-G-A

44762359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350350-C-T

44762411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350411-G-A

http://identifiers.org/hco/7/GRCh38#44762813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6350713-A-C

44762813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350713-A-G

44762813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350713-A-T

44762916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6350805-A-G

44762916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6350805-A-T

44763104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350966-G-T

44763138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351000-G-A

44764360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352348-C-T

44764499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352484-T-C

44764499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352484-T-G

44764521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352506-G-A

44764521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352506-G-T

44764555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352533-T-A

44764555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352533-T-G

http://identifiers.org/hco/7/GRCh38#44764560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352538-C-A

44764560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352538-C-T

http://identifiers.org/hco/7/GRCh38#44764623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352581-C-A

44764623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352581-C-G

44764623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352581-C-T

http://identifiers.org/hco/7/GRCh38#44764635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352593-C-A

http://identifiers.org/hco/7/GRCh38#44764637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352595-C-A

44764637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352595-C-G

44764637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352595-C-T

44765016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6352879-A-G

44765069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352918-A-G

http://identifiers.org/hco/7/GRCh38#44765138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352974-A-C

44765138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352974-A-G

44765156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6352991-G-A

http://identifiers.org/hco/7/GRCh38#44765160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6352995-C-A

http://identifiers.org/hco/7/GRCh38#44765311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353099-C-A

44765311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6353099-C-G

44765359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6353144-C-T

44765452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6353237-C-T

44765566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6353351-C-G

44765566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6353351-C-T

http://identifiers.org/hco/7/GRCh38#44765664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353451-A-C

http://identifiers.org/hco/7/GRCh38#44765806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353564-C-A

44765806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353564-C-G

44765806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353564-C-T

44765829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353586-G-T

44765836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353591-G-A

http://identifiers.org/hco/7/GRCh38#44765901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353612-C-A

44765901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353612-C-T

http://identifiers.org/hco/7/GRCh38#44766040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353693-C-A

http://identifiers.org/hco/7/GRCh38#44766042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353695-C-A

44766045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353698-T-C

http://identifiers.org/hco/7/GRCh38#44766107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353745-C-A

44766107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6353745-C-T

44766315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6353937-C-G

44766315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6353937-C-T

http://identifiers.org/hco/7/GRCh38#44766342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6353964-C-A

44766342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6353964-C-G

44766368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6353989-C-T

44766472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6354091-C-G

http://identifiers.org/hco/7/GRCh38#44766499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6354118-C-A

44766499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6354118-C-T

44766505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6354124-C-T

44766630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6354249-T-C

44766636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6354255-C-T

44766868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354460-G-A

44767214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354734-C-T

44767299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354799-C-G

44767363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354845-T-C

44767365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354847-G-A

44767365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354847-G-C

44767365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354847-G-T

44767477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354952-A-G

44767611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6355085-T-G

http://identifiers.org/hco/7/GRCh38#44767727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6355199-C-A

http://identifiers.org/hco/7/GRCh38#44767733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6355205-C-A

44767733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355205-C-G

44767779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355248-G-T

44767784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355253-G-T

http://identifiers.org/hco/7/GRCh38#44767836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6355300-A-C

44767836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355300-A-G

44767836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355300-A-T

44768020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355473-A-T

http://identifiers.org/hco/7/GRCh38#44768072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6355516-C-A

44768072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355516-C-G

44768072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355516-C-T

44768073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355517-T-A

44768073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355517-T-C

44768073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355517-T-G

44768116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355551-C-T

http://identifiers.org/hco/7/GRCh38#44768193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6355625-C-A

44768193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355625-C-G

44768193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355625-C-T

44768226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355657-G-A

44768226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355657-G-T

44768570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6355962-A-G

44768577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6355969-G-A

http://identifiers.org/hco/7/GRCh38#44768709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6356089-C-A

44768832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: 6356129-C-G

http://identifiers.org/hco/7/GRCh38#44768859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#6356160-C-A

44768859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: 6356160-C-T

44768873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: 6356174-T-C

44769420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: 6356586-G-A

44769420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22229
most severe consequence: 3 prime UTR variant
orthologous variants: 6356586-G-T