41699523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 81954316-G-A

41699544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 81954337-T-C

41699544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 81954337-T-G

http://identifiers.org/hco/22/GRCh38#41699569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954362-A-C

41699569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 81954362-A-G

41699574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 81954367-C-G

41699616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81954409-G-A

41699616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81954409-G-C

41699631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81954424-C-T

http://identifiers.org/hco/22/GRCh38#41699703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954496-C-A

41699703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81954496-C-G

41699703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81954496-C-T

41699727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954520-T-A

41699727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954520-T-C

41699749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954545-T-C

http://identifiers.org/hco/22/GRCh38#41699753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954549-C-A

41699753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954549-C-T

http://identifiers.org/hco/22/GRCh38#41699827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954620-C-A

41699827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954620-C-G

41699827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954620-C-T

41699874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954659-A-G

http://identifiers.org/hco/22/GRCh38#41699876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954661-C-A

http://identifiers.org/hco/22/GRCh38#41700099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81954920-C-A

41700194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81954969-G-A

41700258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955040-G-T

41700512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955252-G-A

41702741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955365-G-A

41703138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955895-C-T

41703172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955929-T-C

http://identifiers.org/hco/22/GRCh38#41703192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81955943-C-A

41703192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955943-C-T

41703198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955949-A-G

http://identifiers.org/hco/22/GRCh38#41703214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81955967-C-A

41703214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81955967-C-T

41703261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81956012-A-G

41703473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81956225-T-C

http://identifiers.org/hco/22/GRCh38#41703478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81956230-C-A

41703497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81956268-G-A

41703497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81956268-G-C

41703497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81956268-G-T

41705633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81957179-G-A

41705655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81957201-A-G

41705704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81957240-T-G

41713990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959308-G-A

41713990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959308-G-C

41713990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959308-G-T

41713991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959309-T-G

41714043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81959360-A-G

41714043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81959360-A-T

41714146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959469-A-G

41714156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959479-G-A

41714156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959479-G-T

41714335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959632-T-C

41714413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81959962-A-G

41714462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81960011-A-G

41715116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81960407-G-A

41715721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961376-G-T

http://identifiers.org/hco/22/GRCh38#41715898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81961678-A-C

41715898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961678-A-G

41715898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961678-A-T

41715983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961750-T-C

41715991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961758-G-A

41715991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961758-G-T

41716024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961784-A-T

http://identifiers.org/hco/22/GRCh38#41716041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81961801-C-A

41716041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 81961801-C-T

http://identifiers.org/hco/22/GRCh38#41716094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81961854-C-A

http://identifiers.org/hco/22/GRCh38#41716123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81961883-C-A

41716123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81961883-C-G

41716123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81961883-C-T

http://identifiers.org/hco/22/GRCh38#41716171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81961931-C-A

41716212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81961970-T-A

41716391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81962079-T-G

41716510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81962152-G-T

41716531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81962173-C-T

41717836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964037-G-A

41717836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964037-G-T

41717900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964091-G-A

41718075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81964130-C-T

41718165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81964220-A-G

http://identifiers.org/hco/22/GRCh38#41718189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81964244-A-C

41718189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81964244-A-G

41718300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964355-G-A

41718300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964355-G-T

41718362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964380-G-A

41718362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964380-G-C

41718362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964380-G-T

41718375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81964393-T-C

http://identifiers.org/hco/22/GRCh38#41723799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81965965-A-C

41723799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81965965-A-T

41723811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81965977-A-T

41723825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81965991-T-C

41723842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966008-G-A

41723842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966008-G-C

41723847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966012-G-A

41723847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966012-G-C

41723847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966012-G-T

41723850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966015-G-A

41723863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966028-G-C

41723863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966028-G-T

41723880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81966044-T-C

41723959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81966114-G-A

41723959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81966114-G-T

41723962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81966117-G-A

41723980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81966135-G-A

41724024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81966179-A-G

41729448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967087-A-G

41729536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967155-T-C

http://identifiers.org/hco/22/GRCh38#41729598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81967213-C-A

41729598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967213-C-T

41729621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967236-A-G

41729621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967236-A-T

41729630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967245-G-A

41729630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967245-G-T

http://identifiers.org/hco/22/GRCh38#41729689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81967299-C-A

41729689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81967299-C-G

41729689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81967299-C-T

41729766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81967376-C-T

41729827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967456-G-A

41729827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967456-G-C

41729827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967456-G-T

41729894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967534-G-T

http://identifiers.org/hco/22/GRCh38#41729898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81967538-C-A

41729902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967557-T-C

41729927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967580-G-A

41729927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967580-G-C

41729927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81967580-G-T

41730592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81969086-C-G

http://identifiers.org/hco/22/GRCh38#41730703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81969170-C-A

41730703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81969170-C-T

41730732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81969182-T-G

41730816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81969245-T-C

http://identifiers.org/hco/22/GRCh38#41730858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81969266-C-A

41730984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81969385-G-A

41731198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81969547-C-T

http://identifiers.org/hco/22/GRCh38#41731872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81969873-C-A

41731967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81969969-G-A

41731967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81969969-G-T

41732033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81970027-G-C

41732149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81970237-A-G

41732182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81970270-G-T

41732270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81970357-G-C

41732270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81970357-G-T

41732279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81970366-C-T

41732290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81970377-A-G

http://identifiers.org/hco/22/GRCh38#41732375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81970448-A-C

41732375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970448-A-T

41732399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970470-G-A

41732399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970470-G-T

41732437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970506-C-T

41732439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970508-C-G

41732439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970508-C-T

41732460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970528-A-T

41732481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81970549-G-A

41732481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81970549-G-T

41732549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81970617-G-T

41732657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970705-G-A

41732657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970705-G-C

41732657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970705-G-T

41732926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81970995-G-A

41739649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81971478-T-C

41739649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81971478-T-G

41739663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81971492-G-A

41739667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81971496-G-A

41739894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81971761-G-A

41740938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81972469-G-T

41740948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81972479-G-A

41743089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81973718-T-C

41743104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81973733-T-C

41743125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81973754-G-C

41743126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81973755-G-A

41743126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81973755-G-T

41743151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81973780-G-A

41743552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975043-A-T

41744839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975377-G-T

41744867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975405-A-G

41744869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975407-G-A

http://identifiers.org/hco/22/GRCh38#41744875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81975413-C-A

41744875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975413-C-T

41744920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975454-G-T

http://identifiers.org/hco/22/GRCh38#41744935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81975469-C-A

41744935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975469-C-G

http://identifiers.org/hco/22/GRCh38#41744950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81975484-C-A

41744950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81975484-C-T

http://identifiers.org/hco/22/GRCh38#41744968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81975505-C-A

41744979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81975516-G-A

41744979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81975516-G-T

41745056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81975593-T-C

41745088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975625-A-G

41745088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975625-A-T

41745098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975628-T-A

41745099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975629-G-A

41745099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975629-G-T

41745104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975634-G-A

41745104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975634-G-T

41745114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975644-A-G

41745116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975646-G-A

41745116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975646-G-C

41745116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975646-G-T

http://identifiers.org/hco/22/GRCh38#41745147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81975672-C-A

41745147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975672-C-G

41745147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975672-C-T

41745244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81975759-G-A

41745301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81976042-G-C

41745321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81976062-C-T

41745344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81976080-G-A

http://identifiers.org/hco/22/GRCh38#41746050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81976981-A-C

41746133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81977014-G-A

41746133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81977014-G-T

41746157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977038-G-C

41747555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977583-T-A

41747555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977583-T-C

41747555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977583-T-G

41747563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977591-G-A

41747563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977591-G-T

41747665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977677-C-T

41747671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977687-G-A

41747671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977687-G-T

41747942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977925-C-T

41747991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81977975-T-G

41748182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81978173-G-A

41748182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81978173-G-C

41748281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978268-G-A

41748281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978268-G-T

http://identifiers.org/hco/22/GRCh38#41748352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81978311-C-A

41748352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978311-C-T

41748367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978326-G-A

41748367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978326-G-C

41748367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81978326-G-T

http://identifiers.org/hco/22/GRCh38#41752387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81979929-C-A

41752387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81979929-C-T

41752463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81979980-G-A

http://identifiers.org/hco/22/GRCh38#41752640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#81980120-C-A

41752640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81980120-C-G

41752640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 81980120-C-T

41752686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980165-G-A

41752686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980165-G-T

41752782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81980260-T-G

41752837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980314-G-A

41752881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980345-C-G

41753098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980533-A-G

41753135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980588-C-T

41753351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81980845-C-T

41753870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81982125-A-G

41753870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81982125-A-T

http://identifiers.org/hco/22/GRCh38#41753940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81982193-C-A

41753940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81982193-C-G

41754016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81982269-C-G

41754016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81982269-C-T

41754064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982317-G-C

41754064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982317-G-T

41754065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982318-A-G

41754104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982354-G-A

41754104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982354-G-T

41754113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982363-A-T

41754126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982374-T-A

41754129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982377-G-A

41754129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982377-G-C

41754129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982377-G-T

41754196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982427-T-A

41754733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982679-A-G

41754807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982721-C-T

41754850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982763-A-T

41754851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982764-C-T

41754903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982815-T-C

41754910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982822-T-G

41755141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81982981-A-G

41755251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983084-T-C

41755281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983119-C-T

41755323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983156-T-C

41755504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983337-A-T

41755867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983748-C-T

41755868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983749-G-A

41755891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81983880-C-T

41756134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984087-G-T

41756485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984249-T-C

http://identifiers.org/hco/22/GRCh38#41756520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984282-C-A

http://identifiers.org/hco/22/GRCh38#41756565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984327-C-A

41756694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984415-G-A

41756751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984471-G-A

http://identifiers.org/hco/22/GRCh38#41756786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984510-C-A

41756902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984552-A-G

http://identifiers.org/hco/22/GRCh38#41757015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984644-A-C

http://identifiers.org/hco/22/GRCh38#41757028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984657-C-A

41757036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984665-C-G

http://identifiers.org/hco/22/GRCh38#41757074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81984712-C-A

41757074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81984712-C-T

41758214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985017-G-T

41758228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985031-G-A

41758228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985031-G-T

http://identifiers.org/hco/22/GRCh38#41758241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81985035-C-A

41758241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985035-C-T

http://identifiers.org/hco/22/GRCh38#41758243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81985037-C-A

41758287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985074-T-A

http://identifiers.org/hco/22/GRCh38#41758306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81985091-C-A

41758306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985091-C-T

41758467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81985251-G-T

41763043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985482-T-C

41763091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985530-G-A

41763132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985571-G-A

41763133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985572-C-G

41763133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985572-C-T

41763142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985597-C-T

41763143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81985598-C-T

41763180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81985635-C-G

41763192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81985647-G-A

http://identifiers.org/hco/22/GRCh38#41763296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81985751-A-C

41763296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81985751-A-G

41770199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81986895-T-G

http://identifiers.org/hco/22/GRCh38#41770324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81986977-C-A

41770325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81986978-C-G

41770423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987094-G-A

41770439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987111-G-A

41770470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987142-A-G

http://identifiers.org/hco/22/GRCh38#41770540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81987206-C-A

41770575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987238-C-T

41770612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987275-A-G

41770612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987275-A-T

http://identifiers.org/hco/22/GRCh38#41770621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81987280-C-A

41770621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987280-C-T

41770654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987313-G-A

41770808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81987463-G-A

41770909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81987564-T-A

41770976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987629-A-G

41770986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81987639-A-G

41772973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81988637-A-G

41773056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81988718-T-C

41773101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81988763-G-A

http://identifiers.org/hco/22/GRCh38#41773256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81988910-C-A

41773405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81989039-T-C

41773983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81989258-G-T

http://identifiers.org/hco/22/GRCh38#41774199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81989439-C-A

41774199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989439-C-G

41774200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989440-T-C

http://identifiers.org/hco/22/GRCh38#41774212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81989450-C-A

41774221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989459-G-T

41774244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989482-A-G

41774248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989486-G-A

41774255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989493-T-C

http://identifiers.org/hco/22/GRCh38#41774261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81989504-C-A

41774261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989504-C-T

41774283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989514-A-G

41774299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989530-G-A

41774331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989563-A-T

41774386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81989611-G-T

41774618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990008-C-G

41774618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990008-C-T

41774645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990035-T-G

41774666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990194-G-A

41774958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990459-T-C

41775296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990775-T-C

41775335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81990814-C-T

http://identifiers.org/hco/22/GRCh38#41775492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81990947-A-C

41775898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991039-A-G

41775900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991041-G-T

41775932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991066-A-G

41775953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991088-G-T

41775961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991096-A-G

41775961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991096-A-T

41776063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81991195-A-G

41776063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81991195-A-T

41776135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991264-C-T

http://identifiers.org/hco/22/GRCh38#41776160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81991289-C-A

41776160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991289-C-G

41776169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991298-G-A

41776173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81991302-G-A

41776173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991302-G-C

41776204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 81991333-C-T

41776215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991344-C-G

41776215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81991344-C-T

41776246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991375-C-T

41776252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81991381-G-A

41776322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991435-G-A

41776344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991459-T-G

http://identifiers.org/hco/22/GRCh38#41776376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81991490-A-C

http://identifiers.org/hco/22/GRCh38#41776386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81991500-C-A

41776386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991500-C-T

41776969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991903-G-A

41776969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991903-G-C

41777060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991945-G-A

41777060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81991945-G-T

41777162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81992032-T-A

41778518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993552-C-T

41778559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993603-T-C

41778624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993661-G-T

http://identifiers.org/hco/22/GRCh38#41778745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81993771-C-A

41778815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81993841-G-A

41778815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81993841-G-T

41778853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81993883-T-C

41778880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81993888-A-G

41778888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81993896-G-A

41778888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81993896-G-T

41778993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993969-C-T

41779006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993982-T-C

41779006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81993982-T-G

41779474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81994057-G-T

41781263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81996625-G-A

41781263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81996625-G-T

41781426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81996789-T-G

41781430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81996793-G-A

41781430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81996793-G-C

http://identifiers.org/hco/22/GRCh38#41781532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81996904-C-A

http://identifiers.org/hco/22/GRCh38#41781558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81996933-C-A

41781600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81996983-C-G

41781600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81996983-C-T

http://identifiers.org/hco/22/GRCh38#41781601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81996984-C-A

http://identifiers.org/hco/22/GRCh38#41781619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81997001-C-A

41781619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81997001-C-T

41781620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81997002-A-G

41781805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81997172-C-G

41781805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81997172-C-T

41781882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997248-T-C

41781883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997249-G-A

41781883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997249-G-T

41781955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997319-G-A

41781955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997319-G-T

41782256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81997785-A-G

41782553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998091-C-G

41782553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998091-C-T

41782566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998104-C-G

41782573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998111-A-G

http://identifiers.org/hco/22/GRCh38#41782591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81998127-A-C

41782591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998127-A-G

41782591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998127-A-T

41782613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81998142-G-A

41783958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999329-C-G

41783969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999340-C-T

41784001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999370-T-C

41784015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999384-C-T

41784123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999454-T-G

41784149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999467-C-T

http://identifiers.org/hco/22/GRCh38#41784190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81999509-C-A

41784190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999509-C-T

http://identifiers.org/hco/22/GRCh38#41784325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81999628-C-A

http://identifiers.org/hco/22/GRCh38#41784331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81999634-C-A

41784334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81999635-G-C

41784334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81999635-G-T

41784428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81999724-T-C

41784428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81999724-T-G

41784434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999730-A-G

41784453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999762-G-C

41784463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999772-T-C

41784478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999787-G-C

41784543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999835-T-C

41784584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81999860-G-A

41784627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81999903-G-A

41784659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81999935-C-G

41784692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81999968-C-T

41784711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81999987-C-T

41784729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82000005-G-A

41784750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 82000026-C-T

41784801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000077-T-C

41784802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000078-G-A

41784802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000078-G-C

41784802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000078-G-T

41784803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000079-G-A

http://identifiers.org/hco/22/GRCh38#41784861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82000148-A-C

41784861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000148-A-T

http://identifiers.org/hco/22/GRCh38#41784869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82000156-C-A

41784869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82000156-C-T

41792993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82006180-G-T

41793696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82007413-T-C

41793696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82007413-T-G

41793729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82007445-G-T

41793808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82007598-T-G

41793825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82007619-G-A

41793825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82007619-G-C

41793825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82007619-G-T

41793855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82007649-T-C

41793884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82007678-A-G

41793933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007724-G-C

http://identifiers.org/hco/22/GRCh38#41793965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82007756-C-A

41793965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007756-C-T

41794040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007788-G-A

41794059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007810-G-C

41794066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007817-A-T

41794088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007838-T-G

41794093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007843-T-A

41794093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007843-T-C

41794169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82007920-A-G

http://identifiers.org/hco/22/GRCh38#41794351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82008073-C-A

41794351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82008073-C-T

http://identifiers.org/hco/22/GRCh38#41794474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82008202-C-A

41794474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 82008202-C-T

41794499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008228-T-C

41794550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008280-C-G

41794550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008280-C-T

http://identifiers.org/hco/22/GRCh38#41794572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82008302-C-A

41794572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008302-C-T

41794610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008339-T-A

41794613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008342-A-G

41795275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008922-A-T

41795307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82008946-G-A

http://identifiers.org/hco/22/GRCh38#41795312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82008951-C-A

41795362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009001-A-T

41795392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009032-G-A

41795392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009032-G-T

http://identifiers.org/hco/22/GRCh38#41795495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82009135-A-C

41795495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82009135-A-G

41795495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 82009135-A-T

41795573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009214-T-C

41795671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009304-A-G

41795713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009334-C-T

41795902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009032-G-A

41795902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009032-G-T

41795959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82009089-A-G

http://identifiers.org/hco/22/GRCh38#41799112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82010673-C-A

41799126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82010687-A-G

http://identifiers.org/hco/22/GRCh38#41799201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82010756-C-A

41799201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82010756-C-T

41799352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82010916-A-G

41799392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 82010954-T-C

http://identifiers.org/hco/22/GRCh38#41799425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#82010987-A-C

41799425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28613
most severe consequence: 3 prime UTR variant
orthologous variants: 82010987-A-G