http://identifiers.org/hco/16/GRCh38#27550247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125307188-C-A

27550247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125307188-C-T

http://identifiers.org/hco/16/GRCh38#27550292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#125307219-A-C

27550292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125307219-A-G

27550292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125307219-A-T

27550453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125307339-A-G

27550557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125307441-G-T

27550818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125307680-G-T

27554622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125310700-T-C

27554664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125310742-G-A

27554664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125310742-G-C

27554740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125310811-C-T

27555287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125311389-C-T

27555316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125311396-C-T

27556121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125311653-T-C

http://identifiers.org/hco/16/GRCh38#27556127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125311659-A-C

27556651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312302-G-C

27556684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312333-T-A

27556684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312333-T-G

27556764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312411-T-C

http://identifiers.org/hco/16/GRCh38#27556815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125312437-C-A

27556815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312437-C-T

27556865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125312485-G-A

http://identifiers.org/hco/16/GRCh38#27558766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125314699-C-A

27558996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125314859-G-A

27559005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125314876-C-T

27559037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125314908-C-T

27559038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125314909-G-A

27559061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125314933-C-T

27559139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125315073-G-A

27559257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125315224-T-G

27560591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125316050-C-T

27560883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125316306-A-T

27563198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125318392-G-A

27563780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319065-G-A

27563892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319199-A-T

http://identifiers.org/hco/16/GRCh38#27563946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125319273-C-A

27564100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319448-C-G

27564100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319448-C-T

27564120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319461-G-A

27564271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125319587-A-T

27566307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320170-G-T

27566320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320183-C-T

27566795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320609-C-G

27566795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320609-C-T

27566868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320652-A-G

27566911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320687-C-T

27566918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320694-C-T

27566922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320698-C-T

27567164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320875-C-T

27567184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320893-A-G

27567235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125320945-T-A

27568991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125323482-G-A

27569047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125323537-A-T

27569239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125323713-C-T

27569333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125323814-T-A

27569573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125324119-T-C

27571524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125324814-G-T

27571787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125325008-A-T

27571807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125325028-A-T

27571880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125325097-G-T

27572329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125325624-A-G

27572345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125325640-C-G

27572774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125326016-G-A

27573359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125326944-C-T

27573442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125327026-C-G

27573474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125327057-G-A

27573540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125327122-A-T

http://identifiers.org/hco/16/GRCh38#27574114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125327628-A-C

27574256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125327740-G-A

27574355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125327832-G-A

27574355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125327832-G-C

27574355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125327832-G-T

27574401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125327867-A-G

27574401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125327867-A-T

27574843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125328252-A-T

27575082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125328437-G-A

27575082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125328437-G-C

27576150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125329159-G-A

27576155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125329164-G-A

27576283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125329290-C-G

27576902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125329678-C-T

27577069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125329801-G-A

http://identifiers.org/hco/16/GRCh38#27579211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125330954-A-C

27579221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125330965-C-T

27579331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125331066-A-G

27579336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125331071-C-G

http://identifiers.org/hco/16/GRCh38#27580800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125332679-A-C

27580800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125332679-A-G

27581209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125332934-G-A

27581542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125333253-G-A

27582304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125333658-G-A

http://identifiers.org/hco/16/GRCh38#27582322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125333687-C-A

27582373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125333734-G-A

27582383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125333744-C-G

27583453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125334922-G-A

27583453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125334922-G-T

http://identifiers.org/hco/16/GRCh38#27583495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125334962-A-C

27583817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125335196-A-T

27590124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125337560-A-G

27590696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338158-A-G

27590707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338168-C-T

27590712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338173-G-A

27590715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338176-T-G

27590717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338178-G-A

27590735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338192-G-A

27590777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338234-C-T

27590781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338238-A-G

27591453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338872-T-C

27591466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125338885-C-T

27591836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125339281-C-T

http://identifiers.org/hco/16/GRCh38#27592108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125339541-C-A

27598287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125342571-T-A

27598357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125343625-C-T

27599680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344077-C-T

27599721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344114-T-A

27599721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344114-T-C

27599758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344156-T-C

27599810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344208-G-A

27599912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344335-G-A

27600151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344574-T-C

27600402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125344995-A-G

27600494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345079-A-G

27600684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345255-C-T

27601192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345434-C-G

27601233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345484-G-A

27601346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345592-G-A

27601797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125345898-C-G

27601977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125346071-C-T

27602068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125346171-C-T

27602282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125346323-G-A

27602336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125346374-A-G

27605649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125347503-G-C

27605819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125347657-G-A

27610583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125348765-G-C

27610583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125348765-G-T

http://identifiers.org/hco/16/GRCh38#27614797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125350738-C-A

27614797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125350738-C-T

27614859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125350814-A-T

http://identifiers.org/hco/16/GRCh38#27618316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125352037-A-C

27618316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352037-A-G

27618316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352037-A-T

27618317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352038-G-A

27618317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352038-G-T

27618339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352059-T-C

http://identifiers.org/hco/16/GRCh38#27618388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125352108-C-A

27618561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352282-T-G

http://identifiers.org/hco/16/GRCh38#27618568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125352289-C-A

27618568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352289-C-T

27618645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352358-A-G

27618734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352447-C-G

27618754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125352452-G-C

27619937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125353641-A-G

27619950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125353654-A-G

http://identifiers.org/hco/16/GRCh38#27620174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125353870-C-A

27620174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125353870-C-T

27620403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125354065-A-G

27620527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125354174-A-T

27620742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125354346-G-A

27625030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125355651-A-G

27625103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125355699-C-T

27625250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125355839-C-T

27625280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125355869-G-A

27625370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125355964-A-T

27626115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125356984-C-G

27626199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125357093-G-A

27626199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125357093-G-C

27626199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125357093-G-T

27626440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125357313-T-A

27626647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125357514-A-G

27628640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125359449-A-G

27628787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125359599-C-T

http://identifiers.org/hco/16/GRCh38#27628816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125359628-C-A

27628816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125359628-C-G

27628816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125359628-C-T

27628880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359691-A-G

27628889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359700-A-G

http://identifiers.org/hco/16/GRCh38#27628975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125359746-C-A

27629174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359782-A-T

27629223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359830-G-A

27629223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359830-G-T

27629241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359850-C-T

27629247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125359856-T-C

27629596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360217-A-G

27629596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360217-A-T

27629623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360243-G-C

http://identifiers.org/hco/16/GRCh38#27630592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125360541-A-C

27630994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360859-A-G

27630994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360859-A-T

http://identifiers.org/hco/16/GRCh38#27631048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125360910-C-A

27631048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125360910-C-T

27631903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125361390-A-G

27632052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125361535-C-T

27633925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362049-G-A

27634084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362206-G-A

27634105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362227-T-C

27634287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362408-G-A

27634287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362408-G-T

27634436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362527-G-A

27634611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362618-G-C

27634733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362737-C-G

27634733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362737-C-T

27636384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362878-C-G

27636501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125362991-C-T

27639297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125365797-C-T

27639823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125366241-C-T

27639926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125366290-G-A

27640274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125366605-C-G

27640274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125366605-C-T

27640724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125366974-A-T

27640825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125367093-G-A

27648637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125369777-C-G

27648637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125369777-C-T

27648713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125369853-A-G

27648713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125369853-A-T

27648757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125369897-T-C

27648757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125369897-T-G

27648868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125370073-G-A

27648868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125370073-G-C

27648868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125370073-G-T

http://identifiers.org/hco/16/GRCh38#27649080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125370313-A-C

27649285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125370502-G-A

27649670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125370662-C-T

27650168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371107-G-A

27650374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371300-T-C

27650431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371365-C-T

27650500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371433-C-G

27650500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371433-C-T

27650533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371463-G-A

27650533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371463-G-T

27650545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371470-A-G

27650667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125371584-A-T

http://identifiers.org/hco/16/GRCh38#27650706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125371607-A-C

27650926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372003-G-A

27651017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372091-A-G

27651056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372142-C-T

27651096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372179-A-G

27651161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372267-A-G

27651228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372342-G-A

27651234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372348-C-T

27651239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372353-A-G

27651489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372601-C-T

27651525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372636-G-A

27651629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125372743-G-A

27651927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125373083-C-T

27652063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125373238-G-T

27652155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125373458-A-G

27652415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125373731-G-A

27654311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375236-G-A

27654390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375301-G-A

http://identifiers.org/hco/16/GRCh38#27654391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125375302-A-C

27654419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375321-G-T

27654433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375333-G-A

27654513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375407-G-A

27654513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375407-G-C

http://identifiers.org/hco/16/GRCh38#27654525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125375419-C-A

27654525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375419-C-T

27654554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125375448-T-C

27654699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125375627-A-G

27654716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125375644-T-C

http://identifiers.org/hco/16/GRCh38#27655643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125376112-A-C

27655643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125376112-A-G

27655674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125376142-G-A

27655974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125376376-T-G

27658528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125377993-G-T

http://identifiers.org/hco/16/GRCh38#27662514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125382995-C-A

27662691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125383149-A-G

27666336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -G-A

27666352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/16/GRCh38#27669167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125389620-A-C

27669167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125389620-A-T

27669212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125389658-A-G

27669292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125389730-C-T

http://identifiers.org/hco/16/GRCh38#27669432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125389861-C-A

27669559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125389987-C-G

27669559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125389987-C-T

27672592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391497-T-C

27672618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391522-T-C

27672618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391522-T-G

27672874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391756-G-A

27672874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391756-G-C

27673000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125391861-G-A

27673497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392275-G-A

27673581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392371-T-A

27673581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392371-T-C

27673581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392371-T-G

27673621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392412-C-G

27673655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392446-C-G

27673655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392446-C-T

27674018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392784-G-T

27674220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392845-G-A

27674220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125392845-G-T

27674518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125393045-T-C

27674591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125393117-C-T

27674602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125393127-G-A

27674618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125393143-G-T

27677625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125394322-T-C

27677625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125394322-T-G

27677737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125394396-A-G

27677944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125394599-T-C

27678048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125394702-A-G

27678108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125394733-G-A

27678127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125394749-T-G

27678242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125394837-A-G

27678347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125394896-C-T

http://identifiers.org/hco/16/GRCh38#27678659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125395196-A-C

27678659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125395196-A-G

http://identifiers.org/hco/16/GRCh38#27678819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125395334-C-A

27678819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125395334-C-T

27681143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396529-A-G

27681313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125396665-G-T

27681353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125396701-C-T

27681514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125396861-G-A

27681521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125396868-A-T

27681562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396907-G-A

27681577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396922-G-A

http://identifiers.org/hco/16/GRCh38#27681610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125396956-C-A

27681633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396977-G-A

27681633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396977-G-T

27681652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125396997-A-T

27681669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125397014-G-T

27683187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125397824-G-A

27683652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125397993-G-A

27683766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125398087-T-C

27685373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125399589-A-G

27685453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125399673-A-T

http://identifiers.org/hco/16/GRCh38#27685461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125399681-C-A

27685593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125399800-C-G

27685727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125399947-C-T

27686426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125400457-G-A

27686544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125400583-G-A

27686552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125400591-G-A

27686739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125400778-T-C

27687152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125401140-G-T

27687186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125401174-G-A

27687410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125401366-A-G

27687518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125401458-T-C

27689591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125404225-G-A

27689625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125404256-A-T

27689706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125404330-C-G

27689733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125404351-A-G

27698147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411766-G-T

http://identifiers.org/hco/16/GRCh38#27698178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125411797-A-C

27698178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411797-A-G

27698215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411843-G-C

27698215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411843-G-T

http://identifiers.org/hco/16/GRCh38#27698247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125411874-C-A

27698247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411874-C-G

27698257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411883-G-T

27698272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411899-G-C

27698304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411930-C-T

27698312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411936-T-A

27698312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411936-T-C

27698524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412157-A-G

27698540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412172-T-C

27698540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412172-T-G

27699102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412594-G-A

27699713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412907-T-A

27700652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413311-G-A

27700695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413355-A-G

27700775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413419-G-C

27700838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413493-A-T

27700967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413612-A-G

27701106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413721-T-C

27701134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413748-G-C

27701134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413748-G-T

http://identifiers.org/hco/16/GRCh38#27701464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125413836-C-A

27701498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125413864-T-A

27701498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125413864-T-C

27701508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125413874-T-C

27701616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125413980-A-G

27701633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125413997-G-A

27701637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125414001-G-T

27701641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125414005-G-A

27701641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125414005-G-C

27701641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125414005-G-T

http://identifiers.org/hco/16/GRCh38#27701702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125414067-C-A

27702240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125414574-A-G

27702800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415092-C-T

27702840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415129-G-A

27703278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415255-C-T

27703437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415346-T-C

27703437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415346-T-G

http://identifiers.org/hco/16/GRCh38#27703782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125415640-C-A

27703782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415640-C-G

http://identifiers.org/hco/16/GRCh38#27704055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125415928-C-A

27704055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415928-C-G

27705989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125416737-T-G

27706008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125416751-T-C

27706027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125416770-T-C

27706887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125417423-C-G

27707025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125417544-C-G

27707459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125417989-C-T

27707732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418240-G-A

27707732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418240-G-T

http://identifiers.org/hco/16/GRCh38#27707784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125418279-C-A

27708382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418893-A-G

27708387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418898-G-A

27708388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418899-T-G

http://identifiers.org/hco/16/GRCh38#27708601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125419056-C-A

27708782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125419217-C-G

http://identifiers.org/hco/16/GRCh38#27708803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125419238-A-C

27717812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426238-C-T

27717841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426270-A-G

27717857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426289-C-T

27717951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426377-G-A

27718126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426542-A-G

27718126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426542-A-T

27718130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426546-A-G

27718134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426568-T-C

http://identifiers.org/hco/16/GRCh38#27718318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125426729-C-A

27718318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426729-C-T

http://identifiers.org/hco/16/GRCh38#27718378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#125426764-C-A

27718378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 125426764-C-T

http://identifiers.org/hco/16/GRCh38#27718428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125426807-C-A

27718428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125426807-C-T

27718458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125426835-G-T

http://identifiers.org/hco/16/GRCh38#27718516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125426891-A-C

27718618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426993-G-C

27718618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426993-G-T

http://identifiers.org/hco/16/GRCh38#27718847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125427148-C-A

27718847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427148-C-T

27718908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427205-G-A

27718908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427205-G-T

27718911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427208-G-A

27718943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427229-T-A

27718943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125427229-T-C

27720918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125428277-C-G

27720974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125428335-T-G

27721004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125428394-G-T

27721076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125428457-T-G

27721433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125428793-G-A

27721704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429047-C-G

27721724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429066-G-A

27721724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429066-G-T

27723505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125430720-A-G

27723505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125430720-A-T

27723608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125430805-G-A

27724091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431263-T-G

27724454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431526-C-T

27724932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431925-C-G

27725262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432192-G-A

27725376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432295-G-T

27725430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432335-G-A

27725552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432458-G-A

27733327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436337-A-G

http://identifiers.org/hco/16/GRCh38#27733661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125436565-A-C

27733677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436577-T-A

27733759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436653-T-C

27733802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436687-G-A

27735048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437417-G-T

27735154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437507-T-G

27735255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437566-C-T

27735563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125437870-T-G

27735688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437996-C-T

27735728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125438036-C-G

27735728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125438036-C-T

27737124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125439222-T-C

27737677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125439598-G-A

27737726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125439649-G-T

27737817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125439740-C-T

27738144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440017-C-T

27738232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440131-A-G

27738253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440238-G-T

27738413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440411-C-T

27738497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440489-C-T

http://identifiers.org/hco/16/GRCh38#27738541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125440536-A-C

27738565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440566-C-T

27738661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440633-G-A

27738717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440679-C-T

27739863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441583-C-T

27739890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441610-T-C

http://identifiers.org/hco/16/GRCh38#27739897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125441616-A-C

27739936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441653-A-G

27739989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441700-T-C

27740007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441718-T-C

27740228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125441939-A-G

27740264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125441975-G-A

http://identifiers.org/hco/16/GRCh38#27740402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442110-C-A

27740402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125442110-C-T

http://identifiers.org/hco/16/GRCh38#27740510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442218-A-C

27740510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125442218-A-G

27740510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125442218-A-T

http://identifiers.org/hco/16/GRCh38#27740567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442275-C-A

27740659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125442367-C-T

http://identifiers.org/hco/16/GRCh38#27740679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442387-C-A

27740679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125442387-C-T

http://identifiers.org/hco/16/GRCh38#27740786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442494-C-A

27740983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442657-G-A

http://identifiers.org/hco/16/GRCh38#27740984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442658-C-A

27740984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442658-C-T

http://identifiers.org/hco/16/GRCh38#27741036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125442710-C-A

27741036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442710-C-G

27741036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442710-C-T

27741060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442735-T-A

27741060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442735-T-C

27743547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444635-G-C

27743713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444783-T-G

27744072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445099-A-G

27744126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445155-A-G

27744140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445169-G-A

27745622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445701-G-A

27745690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445772-T-C

27745690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125445772-T-G

27746361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446358-G-T

27746387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446383-G-A

27746387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446383-G-T

27746503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446480-C-T

27746625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446622-G-T

27746630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446627-A-T

27746696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446666-C-G

27746840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446778-G-A

27746875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125446811-G-T

27747037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125447096-G-A

27747302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125447561-G-A

27747377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125447628-G-A

27747596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125447848-G-A

27747792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125447971-C-T

27747978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448141-C-G

27747978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448141-C-T

27748005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448168-G-A

27748018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448193-T-G

27748251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448423-T-C

27749298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125449150-C-G

27749309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 125449161-A-G

http://identifiers.org/hco/16/GRCh38#27749529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125449419-C-A

27749804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125449694-G-T

27749839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125449708-C-G

27749839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125449708-C-T

27749912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125449781-C-T

27750267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125450136-G-A

http://identifiers.org/hco/16/GRCh38#27750278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125450147-C-A

27750278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125450147-C-T

http://identifiers.org/hco/16/GRCh38#27751476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125450888-C-A

27751476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450888-C-G

27751576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450965-A-G

27751868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125451258-G-A

http://identifiers.org/hco/16/GRCh38#27752032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125451526-C-A

27752032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451526-C-G

27752032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451526-C-T

27752036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451530-T-C

http://identifiers.org/hco/16/GRCh38#27752044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125451538-C-A

27752164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451644-C-G

27752222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451712-G-A

27752904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125452402-T-C

http://identifiers.org/hco/16/GRCh38#27753379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125452849-C-A

27753427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125452883-C-G

27753436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125452890-G-A

27753597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453059-G-A

27753731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453224-T-C

27753731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453224-T-G

27753739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453232-C-T

27753758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453265-T-C

27753999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453533-G-A

27753999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453533-G-T

27754024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453585-C-T

27754046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453618-G-T

27754154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453713-T-C

27754170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125453729-C-T

http://identifiers.org/hco/16/GRCh38#27754250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125453809-C-A

27754250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 125453809-C-T

27754476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125453885-G-A

27754476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125453885-G-T

http://identifiers.org/hco/16/GRCh38#27754542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125453931-C-A

http://identifiers.org/hco/16/GRCh38#27754842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125454140-C-A

http://identifiers.org/hco/16/GRCh38#27754852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125454150-C-A

27754852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125454150-C-T

http://identifiers.org/hco/16/GRCh38#27754984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125454232-C-A

27754984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125454232-C-T

27755303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125454520-A-G

27755341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125454550-T-G

27755457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125454648-C-T

27756405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125455532-T-C

27756405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125455532-T-G

27756794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125455910-T-G

27757536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125456457-C-G

http://identifiers.org/hco/16/GRCh38#27757578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125456498-C-A

27757583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125456503-G-A

27757706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125456606-A-G

27758206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125457052-C-T

27758310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125457149-C-T

27758623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125457529-C-T

27758911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125457777-G-C

27759369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125458107-T-C

27759446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125458179-C-T

http://identifiers.org/hco/16/GRCh38#27759482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125458209-A-C

27759913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125458523-T-G

27760082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125458676-C-G

27760465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125459012-G-T

27760951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125459396-G-A

27761091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125459502-G-C

http://identifiers.org/hco/16/GRCh38#27761334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125459642-C-A

http://identifiers.org/hco/16/GRCh38#27761375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125459664-C-A

27761375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125459664-C-G

27761375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125459664-C-T

http://identifiers.org/hco/16/GRCh38#27761394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125459683-A-C

27761492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125459779-G-A

27761529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense variant
orthologous variants: 125459816-G-A

27761558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125459845-C-T

27761827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460028-C-T

27761838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460039-G-T

27762253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460377-C-T

27762404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460499-T-G

27762414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460509-A-G

27762437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460525-A-G

27762512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125460606-T-C

27762971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125461032-C-T

27764806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125463347-T-C

27764851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125463389-G-A

27764907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125463445-C-T

27765473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125463822-T-G

27766208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464359-G-A

27766208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464359-G-T

27766211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464362-G-A

27766223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464372-T-C

27766224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464373-T-C

27766224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464373-T-G

27766491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464598-T-C

http://identifiers.org/hco/16/GRCh38#27766523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125464622-C-A

27766523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464622-C-T

27766527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464623-T-A

http://identifiers.org/hco/16/GRCh38#27766582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125464678-C-A

27766582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464678-C-G

27766582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464678-C-T

27766594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464690-G-A

27766597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464693-G-A

27766597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464693-G-T

27766599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464694-G-A

27766599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464694-G-T

27766723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125464792-C-T

27769822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, undefined
orthologous variants: 125465472-C-G

27769822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, undefined
orthologous variants: 125465472-C-T

27769880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense variant
orthologous variants: 125465517-C-T

27771588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 125466775-G-A

27773033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125467855-G-T

27773044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125467864-A-G

27773044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125467864-A-T

27773088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125467901-A-G

http://identifiers.org/hco/16/GRCh38#27773175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125467987-C-A

27773175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125467987-C-T

http://identifiers.org/hco/16/GRCh38#27773196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125468008-C-A

27773196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125468008-C-T

http://identifiers.org/hco/16/GRCh38#27773332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125468320-C-A

27773332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468320-C-T

27773366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468445-G-A

27773366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468445-G-C

27773536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468626-G-A

27773760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468802-C-T

27773761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468803-A-G

27773825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125468852-C-T

27774108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125469118-A-G

27774313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125469250-A-G

27774394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125469324-T-C

27774475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125469393-G-C

http://identifiers.org/hco/16/GRCh38#27774857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125469715-A-C

27774857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125469715-A-G

27775021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125469891-C-T

27775042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: synonymous variant
orthologous variants: 125469912-T-C

http://identifiers.org/hco/16/GRCh38#27775147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125469991-C-A

27775272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470083-A-T

27775296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470128-C-T

27775367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470198-C-T

27775920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470606-G-A

27775920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470606-G-C

27775951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125470637-G-A

27776683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125471087-G-A

27776686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125471089-A-G

27776823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron variant
orthologous variants: 125471225-C-T

27776993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125471388-T-C

27777149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471540-G-C

27777149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471540-G-T

27777255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471597-G-A

27777542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471794-G-A

27777542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471794-G-C

27777542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471794-G-T

27777544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471796-G-A

27777544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471796-G-C

27777544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471796-G-T

http://identifiers.org/hco/16/GRCh38#27777547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125471799-C-A

http://identifiers.org/hco/16/GRCh38#27777551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125471803-C-A

27777551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471803-C-T

27777562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471814-G-A

27777571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471823-A-G

27777573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471825-G-A

27777573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125471825-G-C

27777627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125471876-G-A

27777627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125471876-G-C

27777643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125471892-A-G

27777878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125472101-C-T

http://identifiers.org/hco/16/GRCh38#27777929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125472152-C-A

http://identifiers.org/hco/16/GRCh38#27778077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125472286-C-A

27778077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472286-C-T

27778302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472389-G-T

27778518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472594-C-T

27778555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472600-C-G

27778563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472608-T-C

27778563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125472608-T-G

http://identifiers.org/hco/16/GRCh38#27778711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125472757-C-A

27778711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125472757-C-G

27778767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125472808-G-T

http://identifiers.org/hco/16/GRCh38#27778906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125472950-A-C

27778912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125472956-G-A

27778912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125472956-G-C

http://identifiers.org/hco/16/GRCh38#27779107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125473102-C-A

27779107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473102-C-T

27779139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473120-T-A

27779139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473120-T-C

27779152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473133-G-A

27779152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473133-G-T

27779287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473209-G-A

27779287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473209-G-T

27779730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473359-G-A

27779730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473359-G-C

http://identifiers.org/hco/16/GRCh38#27779734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125473363-C-A

http://identifiers.org/hco/16/GRCh38#27779844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125473479-C-A

27779871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473504-G-A

27779871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473504-G-T

27780166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473770-T-C

27780166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473770-T-G

27780174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473778-G-T

27780205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473823-A-G

27780241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29068
most severe consequence: 3 prime UTR variant
orthologous variants: 125473850-T-C