http://identifiers.org/hco/2/GRCh38#149330083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49956060-C-A

149330083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5 prime UTR variant
orthologous variants: 49956060-C-G

149330083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5 prime UTR variant
orthologous variants: 49956060-C-T

http://identifiers.org/hco/2/GRCh38#149330114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#49956091-C-A

149330114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 49956091-C-T

149330154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 49956110-G-A

149330154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 49956110-G-T

149330172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 49956128-G-A

149330188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5 prime UTR variant
orthologous variants: 49956141-G-A

149330284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron_variant, undefined
orthologous variants: 49956233-C-T

http://identifiers.org/hco/2/GRCh38#149330380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49956286-C-A

149330428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 49956335-C-G

149330428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 49956335-C-T

http://identifiers.org/hco/2/GRCh38#149330486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49956393-A-C

http://identifiers.org/hco/2/GRCh38#149330608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49956485-C-A

149330608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49956485-C-G

149330685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49956561-G-A

149330774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49956651-C-T

149330853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49956686-T-C

149330981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 49956780-G-A

149331053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49956833-T-G

149331343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957077-C-T

149331680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957332-T-C

149331766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957418-C-T

149331836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957488-T-C

149331979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957609-T-A

149332083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957700-G-A

149332154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957771-T-C

149332262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49957861-T-C

149332404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958005-G-A

149332446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958043-C-G

149332569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958139-T-G

http://identifiers.org/hco/2/GRCh38#149332587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49958162-A-C

149332668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958241-T-G

149332717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958315-C-T

149333455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958809-G-A

149333474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49958828-C-T

149333712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49959013-C-T

149333797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49959097-C-G

http://identifiers.org/hco/2/GRCh38#149333987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49959267-A-C

149333987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49959267-A-G

149334706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49959932-A-G

149334776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49959992-A-T

149336126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960100-T-C

http://identifiers.org/hco/2/GRCh38#149336145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49960111-C-A

149336288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960251-A-G

149336377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960326-A-G

149336511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960448-G-A

149336553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960488-A-G

149336679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960724-G-A

149336715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49960760-C-G

149336771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961019-A-G

149336797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961045-T-C

149336797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961045-T-G

149336820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961068-T-A

149337027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961247-C-T

149337239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961406-T-C

149337565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961704-G-A

149337565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961704-G-T

149338647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49961924-C-G

149338736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962013-A-T

149338759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962036-C-T

149338806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962083-T-C

149338811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962088-G-C

149339013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962276-C-T

149339273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962389-T-C

149339314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962436-A-G

149339348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962473-G-A

149339534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962659-A-G

149339578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962692-G-C

149339708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962825-A-G

149339738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49962856-T-A

http://identifiers.org/hco/2/GRCh38#149339752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49962870-C-A

149339903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49963014-T-C

149340313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49965105-G-A

149340346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49965132-A-G

149340574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49965355-A-G

149340927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49965675-C-T

149341301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966036-C-T

149341308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966043-A-T

149341377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966110-C-G

149341377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966110-C-T

149341383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966116-C-T

149341393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966126-T-C

149342439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49966665-T-A

http://identifiers.org/hco/2/GRCh38#149342484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49966716-A-C

149342708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967323-C-T

149342792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967399-G-T

149342913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967499-G-C

149342913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967499-G-T

149343024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967605-G-A

149343125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967707-G-A

149343365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49967920-G-A

149343587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968130-G-A

149343593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968136-T-C

149343671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968209-G-A

149343682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968219-G-A

http://identifiers.org/hco/2/GRCh38#149343855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49968371-C-A

149343855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968371-C-T

149343951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968575-C-T

149344001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968622-A-G

http://identifiers.org/hco/2/GRCh38#149344099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49968725-C-A

149344099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968725-C-G

149344099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968725-C-T

149344164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968792-A-G

149344315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49968930-C-T

149346057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49970651-C-T

149346316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49970915-A-G

149346384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49970973-T-A

149346384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49970973-T-C

149347082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971432-G-A

149347155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971473-G-C

149347219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971496-A-G

149347262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971539-A-T

149347395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971682-T-A

149347395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971682-T-C

149347429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49971716-C-T

http://identifiers.org/hco/2/GRCh38#149347781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49972617-C-A

149348724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974073-A-G

149348853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974204-T-G

149349018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974368-G-A

149349018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974368-G-C

149349193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974514-T-C

149349290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974609-G-A

149349609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974893-T-C

149349653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49974941-A-G

149350016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975289-C-G

149350038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975311-C-T

http://identifiers.org/hco/2/GRCh38#149350149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49975431-C-A

149350269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975575-A-G

http://identifiers.org/hco/2/GRCh38#149350362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49975672-A-C

149350543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975865-A-G

149350584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975908-T-C

149350622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975943-A-G

149350656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49975972-T-G

149350862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976154-A-G

149350970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976277-G-T

http://identifiers.org/hco/2/GRCh38#149351366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49976433-C-A

149351366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976433-C-T

149351482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976471-G-C

149351760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976741-G-C

149351798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976777-C-T

149351805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976784-T-A

149351854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976833-C-G

149351928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49976868-T-C

149352662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977140-G-A

149352662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977140-G-T

149352715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977193-A-G

149352715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977193-A-T

149352969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977434-A-G

149353193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977643-G-A

149353193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977643-G-C

149353534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49977974-G-A

http://identifiers.org/hco/2/GRCh38#149353634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49978076-C-A

149353634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49978076-C-G

149353869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49978286-G-A

149353975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49978390-G-T

149354566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49979636-A-G

149354800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49979870-G-A

149354965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980021-C-T

149354977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980033-G-A

149355404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980438-A-T

149355423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980480-C-G

149355443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980500-G-C

149355443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980500-G-T

149356039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980954-A-G

149356047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49980962-A-G

http://identifiers.org/hco/2/GRCh38#149356352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49981194-C-A

149356971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49981738-T-C

149357329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982098-T-C

149357368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982136-T-C

149357369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982137-T-G

149357378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982146-C-T

149357427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982192-A-G

149357503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982268-T-C

149357547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982311-G-T

http://identifiers.org/hco/2/GRCh38#149357558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49982322-A-C

149357754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982580-A-T

149358314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982756-C-T

149358535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49982852-C-T

149359061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49983381-A-G

149362160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986057-G-A

149362310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986190-T-G

149362334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986200-C-T

149362409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986264-C-T

149362482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986332-T-A

149363032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49986665-G-A

149363595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987177-G-A

149363677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987243-C-T

149363714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987280-A-G

149363746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987308-G-A

149363757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987319-A-G

149363890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987451-G-A

149364009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987563-G-A

149364009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49987563-G-C

149364458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988075-C-T

149364541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988152-A-T

149364721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988327-C-T

149365081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988674-A-G

149365130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988747-G-A

149365130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988747-G-T

149365133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49988750-G-A

149365359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49989139-T-C

149365427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49989204-G-C

149365767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49989485-A-G

149365831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49989550-T-A

http://identifiers.org/hco/2/GRCh38#149366018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49990156-C-A

149366018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990156-C-T

149366167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990288-T-G

149366376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990486-C-G

149366560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990666-G-A

149366597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990706-A-G

149366723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990832-G-C

149366876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49990984-C-T

149366967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991076-C-G

149367205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991324-A-G

http://identifiers.org/hco/2/GRCh38#149367228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49991345-A-C

149367228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991345-A-T

149367283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991395-G-A

149367395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991506-C-T

149367560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991655-T-C

149367606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991701-G-A

149367606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991701-G-T

149367630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991729-A-G

149367794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991868-T-C

149367815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49991888-G-T

149367932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49991993-G-T

149367944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992005-A-G

149367963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992023-T-A

149367963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992023-T-C

149367963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992023-T-G

149367964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992024-T-A

149368009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49992095-G-A

149368037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49992283-T-C

149368059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49992301-G-A

149368059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49992301-G-T

149368065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 49992307-A-G

149368174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992408-T-G

http://identifiers.org/hco/2/GRCh38#149368362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49992577-C-A

149368684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992705-A-T

149368808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992791-A-G

149368816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49992799-A-G

http://identifiers.org/hco/2/GRCh38#149369195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49993113-C-A

149369201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49993119-A-G

149369460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49993350-A-G

149369587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49993496-G-A

149369999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49993994-G-A

149369999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49993994-G-T

149370011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994006-C-T

149370178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994177-G-C

149370341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994330-C-T

149370377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994359-G-A

149370377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994359-G-T

149370469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994436-G-A

149370469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994436-G-C

149370469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994436-G-T

149370490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994472-G-C

http://identifiers.org/hco/2/GRCh38#149370500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49994483-C-A

149370500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994483-C-T

149370617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 49994601-T-C

149370660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994640-C-T

149370764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994739-A-G

149370947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49994993-A-G

149370976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995027-A-G

149370991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995043-A-G

149370994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995046-G-A

149371085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995120-G-A

149371340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995358-A-G

149371475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995509-T-G

149371502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995536-G-A

149371502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995536-G-C

149371527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995572-A-G

149371532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995605-T-A

149371631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995703-A-G

149371844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995894-T-A

149371844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49995894-T-C

http://identifiers.org/hco/2/GRCh38#149371855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49995905-C-A

149372216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996255-C-T

149372271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996308-G-A

149372271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996308-G-T

149372483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996439-A-G

149372554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996488-A-G

149372593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996527-G-C

149372606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996540-T-C

149372719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996656-G-A

149372763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49996693-G-T

149372898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49997789-G-C

149372931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49997820-T-C

149372974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49997859-C-G

149373002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49997887-T-A

149373150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49998017-G-A

149373415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49998307-A-T

149373969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49998806-G-A

http://identifiers.org/hco/2/GRCh38#149374049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#49998884-A-C

149374107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49998939-T-C

149374287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999152-G-A

149374532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999339-T-G

149375120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999554-G-T

149375161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999595-G-A

149375253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999721-G-A

149375253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999721-G-T

149375375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999834-A-G

149375397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 49999858-A-G

149375687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000101-C-T

149375717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000130-T-C

149375732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000145-T-A

149375901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000308-A-G

149375955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000371-G-A

149376025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000441-C-T

149376114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000529-C-T

149376133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000547-G-A

149376133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000547-G-T

http://identifiers.org/hco/2/GRCh38#149376234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50000651-C-A

149376311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000712-G-C

149376538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000930-A-G

149376585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50000977-T-C

149376906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50001286-C-T

149377167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50001571-G-C

149377200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50001614-T-A

http://identifiers.org/hco/2/GRCh38#149377323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50001733-A-C

149377426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50001824-A-T

149378566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50002308-C-T

149379556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50004178-C-T

149381122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50006197-A-G

149381817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50006671-A-G

149382262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007135-G-A

149382339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007207-G-A

149382472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007329-C-T

149382574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007418-C-T

149382796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007626-C-G

149382861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007692-A-G

149382884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50007721-T-A

149383695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50008497-T-C

http://identifiers.org/hco/2/GRCh38#149383772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50008566-A-C

149384345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009085-G-A

149384416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009152-A-T

149384435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009172-G-A

149384435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009172-G-T

149384437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009174-C-T

http://identifiers.org/hco/2/GRCh38#149384482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50009219-C-A

149384492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009229-G-A

149385302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009733-G-A

149385400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009810-G-T

149385513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50009921-C-T

149385671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010079-G-A

149385719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010153-G-C

149385856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010530-A-G

149385908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010640-G-A

http://identifiers.org/hco/2/GRCh38#149386007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50010737-C-A

149386007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010737-C-G

149386007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010737-C-T

149386041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010769-T-C

149386164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50010931-G-C

http://identifiers.org/hco/2/GRCh38#149386458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50011219-C-A

149386458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50011219-C-T

149386615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50011372-C-T

149387000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50011724-G-A

149387255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50011958-G-A

149387578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50012265-T-C

149387728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50012476-G-A

149387743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50012491-T-C

149387962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50012684-G-A

http://identifiers.org/hco/2/GRCh38#149388299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50013565-A-C

149388931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014255-C-G

149389062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014385-A-G

http://identifiers.org/hco/2/GRCh38#149389188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50014511-C-A

149389213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014536-G-A

149389367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014690-A-G

149389442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014766-C-T

149389503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014830-A-G

149389542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014869-C-T

149389591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50014916-A-G

149389802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015100-T-G

http://identifiers.org/hco/2/GRCh38#149389803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50015101-A-C

149390081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015189-A-G

149390084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015192-C-T

149390184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015293-G-A

149390334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015439-T-C

149390356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015461-T-A

149390511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015613-T-A

149390609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50015706-T-C

http://identifiers.org/hco/2/GRCh38#149390644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50015755-A-C

149391008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50016565-A-G

149391314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50016857-A-G

149391470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50017129-C-T

http://identifiers.org/hco/2/GRCh38#149391520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50017319-A-C

149391712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50017500-C-T

149391739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50017527-A-G

149391783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50017575-G-A

149392254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50017975-G-A

149392492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018185-C-T

149392555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018250-C-T

149392630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018343-C-T

149392653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018376-T-C

149393184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018603-T-C

149393425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50018841-G-C

149393703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50019122-T-C

149393843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50019258-C-T

149393866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50019282-A-T

http://identifiers.org/hco/2/GRCh38#149393999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50019639-C-A

149394041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50019681-T-C

149397570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50027322-A-G

149400328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50028793-C-G

149400328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50028793-C-T

149400467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50028917-T-C

149400702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029088-T-G

149400922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029337-A-G

149401005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029414-C-T

149401216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029499-G-A

149401216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029499-G-T

149401219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029502-C-T

149401464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50029724-G-A

http://identifiers.org/hco/2/GRCh38#149401679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50029906-C-A

149410358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030157-G-C

149410607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030406-G-A

149410612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030411-T-A

149410645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030496-C-T

149410673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030618-T-C

149410845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030779-A-G

149410941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50030868-C-G

149411145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50032677-C-T

149411353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50032887-G-A

149411454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50032976-G-T

149411686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50033212-T-C

149413477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50033501-A-G

149413900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50033900-G-A

149414113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50034152-G-A

149414161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50034179-C-T

http://identifiers.org/hco/2/GRCh38#149414939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50035406-C-A

149414939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50035406-C-T

149414995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50035524-A-T

149415460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50035950-T-C

http://identifiers.org/hco/2/GRCh38#149415530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50036029-A-C

149415673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036131-C-G

149416095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036272-G-A

http://identifiers.org/hco/2/GRCh38#149416146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50036302-C-A

http://identifiers.org/hco/2/GRCh38#149416279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50036392-A-C

149416279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036392-A-G

http://identifiers.org/hco/2/GRCh38#149416283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50036396-A-C

149416333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036433-A-G

149416346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036446-G-A

149416613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036643-C-T

149416717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036754-C-T

149416718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036755-C-G

http://identifiers.org/hco/2/GRCh38#149416731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50036770-C-A

149416869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036890-G-T

149416922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50036933-T-A

149417012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037017-C-T

149417036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037037-T-C

149417053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037052-G-A

149417113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037086-C-G

149417290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037265-A-G

149417315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037289-G-A

149417567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037565-T-C

149417669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037661-A-G

http://identifiers.org/hco/2/GRCh38#149417849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50037859-C-A

149417849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50037859-C-G

149417990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038010-G-A

149418061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038274-G-C

149418205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038399-C-T

149418301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038500-A-T

149418368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038560-C-T

149418545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038729-A-G

149418662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038842-G-A

149418662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038842-G-T

149418676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50038855-G-A

149418900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50039664-T-G

149418902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50039666-A-G

http://identifiers.org/hco/2/GRCh38#149418962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50039727-A-C

149419272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040009-G-A

149419273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040010-C-T

149419542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040301-G-A

149419641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040409-G-A

149419752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040537-C-T

149419814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040598-A-G

149419928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040692-T-C

149419977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040742-C-T

149420092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040851-A-G

149420104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040864-G-A

149420130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50040883-G-A

149420229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040983-C-T

149420230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50040984-G-A

149420373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041101-T-G

149420473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041202-T-C

149420537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041265-G-C

http://identifiers.org/hco/2/GRCh38#149420551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50041279-A-C

http://identifiers.org/hco/2/GRCh38#149420865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50041592-C-A

149420875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041602-T-C

149420914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041640-G-A

149420983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041714-C-T

149421053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50041779-A-G

149421416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042163-G-T

149421430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042176-A-G

149421430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042176-A-T

149421509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042243-G-A

149421509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042243-G-C

149421726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042451-A-G

149421851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042577-G-A

149421855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042581-A-G

149421887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042611-A-G

149421887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042611-A-T

149421974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042698-T-C

149422124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50042850-T-C

http://identifiers.org/hco/2/GRCh38#149422292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#50043027-C-A

149422531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50043882-T-C

149422769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044098-C-G

http://identifiers.org/hco/2/GRCh38#149422798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50044127-C-A

149422925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044225-A-G

149423079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50044361-G-T

149423137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50044411-G-A

149423240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50044497-G-A

149423282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044539-A-G

149424859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044599-C-G

149424883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044628-C-G

149424932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50044698-A-G

149425451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50045390-A-G

149425637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50045676-T-C

149425753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50045789-C-T

http://identifiers.org/hco/2/GRCh38#149426023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50046041-A-C

149426343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50047080-A-G

149426350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50047087-G-A

http://identifiers.org/hco/2/GRCh38#149426522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50047243-A-C

149426974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50047640-A-G

149427106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50047780-T-C

149427140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50047807-G-C

149427264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50048139-C-T

149427957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50048952-C-T

149427985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50048980-G-C

149428066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049063-C-T

149428116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049113-A-G

149428154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049152-C-T

149428258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049263-T-G

149428439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049437-G-A

149428524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049515-C-T

149428573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049560-C-T

149428654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049637-A-G

149428664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049661-A-G

149428680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049677-C-G

149428680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049677-C-T

149428721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049704-G-A

149428744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50049723-T-C

149429184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050005-A-T

149429562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050353-A-G

149430613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050617-G-T

149430713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050717-A-G

149430821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050833-T-C

149430985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50050991-C-T

149431017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051023-A-T

149431251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051261-C-T

149431366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051378-C-T

http://identifiers.org/hco/2/GRCh38#149431416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50051413-A-C

149431416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051413-A-G

149431684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051654-T-C

149431752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051725-A-G

149431803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50051775-G-T

149432059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50052262-A-G

http://identifiers.org/hco/2/GRCh38#149432082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50052285-C-A

149432169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50052377-G-C

149432381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50052565-T-C

149433006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50053033-A-T

149433041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50053065-G-A

149433078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50053104-C-T

149436995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50054860-T-C

149437082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50054943-G-T

149437175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055035-T-G

149437210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055062-C-T

149437449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055289-T-C

149437657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50055500-G-A

149437657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 50055500-G-T

149437870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055728-A-G

149437870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055728-A-T

149437872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055730-A-G

149437933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055787-G-T

149437947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055801-G-A

149437947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055801-G-T

149438016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055861-T-G

149438069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50055913-T-G

149438190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056032-G-A

149438279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056111-T-C

149438415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056247-C-T

149438459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056368-T-A

149438459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056368-T-C

149438492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056433-T-G

149438560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056543-C-T

149438655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056610-C-T

149438710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056667-C-G

149438841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50056761-T-C

149439262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50057806-A-G

149439505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058008-A-G

149439676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058171-G-A

149439676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058171-G-T

149439677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058172-G-C

149440511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058502-A-G

149440526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058519-G-T

149440538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058530-G-T

149440542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058534-A-G

149441029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058631-A-G

149441107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058712-T-C

149441128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50058733-A-G

149441651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50059252-C-T

149441706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50059337-C-T

149441882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50059502-C-T

149441897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50059517-T-G

http://identifiers.org/hco/2/GRCh38#149442227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50059830-C-A

149442572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50060184-C-G

149442572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50060184-C-T

149442573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50060185-G-A

149442573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50060185-G-T

http://identifiers.org/hco/2/GRCh38#149442599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50060211-C-A

149442825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50060431-T-C

149443495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50061331-T-C

http://identifiers.org/hco/2/GRCh38#149446633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50061734-C-A

149446633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50061734-C-T

149446708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50061807-G-A

149446708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50061807-G-T

http://identifiers.org/hco/2/GRCh38#149447161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50062250-A-C

149447171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50062260-C-T

149448940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063511-G-A

149448940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063511-G-T

http://identifiers.org/hco/2/GRCh38#149448950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50063521-C-A

149448950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063521-C-G

149448993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063558-A-G

http://identifiers.org/hco/2/GRCh38#149449050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50063614-C-A

149449050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 50063614-C-G

149449050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 50063614-C-T

149449056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 50063620-A-G

149449197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063759-A-G

149449252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063798-G-A

149449252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063798-G-C

149449252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063798-G-T

149449375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50063925-A-G

149449838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064387-G-A

149449987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064508-C-T

http://identifiers.org/hco/2/GRCh38#149450069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50064590-A-C

http://identifiers.org/hco/2/GRCh38#149450150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50064651-A-C

149450150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064651-A-G

149450381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064860-A-G

149450457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064904-T-G

149450501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50064936-T-C

http://identifiers.org/hco/2/GRCh38#149450544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50064988-C-A

149450606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065075-A-G

149450673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065149-T-C

http://identifiers.org/hco/2/GRCh38#149450719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50065204-C-A

149450910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065416-C-T

149451157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065607-G-A

149451157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065607-G-C

149451214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065664-A-T

149451216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065666-C-T

149451261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065713-A-G

149451361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065810-T-C

149451361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065810-T-G

149451487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065933-A-G

149451548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50065975-T-A

149451645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50066081-C-T

149451882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50066326-G-T

149451955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50066398-G-A

149452028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 50066464-C-T

149452075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50066510-T-C

149452120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067120-A-G

149452419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067387-A-G

149452487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067463-C-T

149452697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067665-C-T

149452850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067823-A-G

149452931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067880-T-C

149452944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50067894-G-T

http://identifiers.org/hco/2/GRCh38#149453169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50068060-C-A

149453169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068060-C-T

149453562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068383-A-G

149453651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068470-G-C

149453784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068571-G-A

149453823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068618-G-T

149453992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068750-C-T

149454204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068915-A-G

149454204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50068915-A-T

http://identifiers.org/hco/2/GRCh38#149454214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50068925-A-C

149454324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50069032-A-G

149454327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50069035-A-G

149454608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50069318-A-G

http://identifiers.org/hco/2/GRCh38#149454653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50069362-A-C

149454945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50069628-G-A

149455049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50069731-G-A

149455817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50070661-G-T

149455823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50070666-T-A

149456013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50070980-G-A

149456065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071010-A-G

149456070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071015-T-G

149456223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071164-T-C

149456295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071222-G-A

149456363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071292-G-C

149456822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071724-A-G

149456922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071802-C-T

149456981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50071853-A-G

149457151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072241-T-C

149457156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072262-G-A

149457188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072293-G-A

149457221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072330-G-A

149457497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072613-A-G

149457700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072762-T-G

149457766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072827-A-G

149457808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072861-T-A

149457856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50072922-A-G

http://identifiers.org/hco/2/GRCh38#149457966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50073068-A-C

149458231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50073324-G-C

149458275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50073368-A-G

149458402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50073477-C-T

149458462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50073532-C-T

149464898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075037-G-A

149464983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075109-G-A

149465101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075199-A-G

149465126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075223-G-T

149465129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075226-T-C

149465135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075232-C-T

149465291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075357-G-T

149465383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075433-G-A

149465565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075593-T-C

149465613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50075693-C-T

149466104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076165-A-G

149466191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076256-A-T

149466583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076660-T-G

149466587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076664-T-G

149466657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076720-G-C

149466875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50076937-T-C

149467106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077133-G-A

149467133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077162-A-G

149467650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077653-A-G

149467715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077718-A-G

149467837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077817-C-T

149467947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077905-T-C

http://identifiers.org/hco/2/GRCh38#149467960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50077918-C-A

149467982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50077935-A-G

149468196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078098-T-A

149468300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078189-A-G

149468372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078263-A-T

149468600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078675-T-C

149468757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 50078835-C-T

149468914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078958-T-C

149468914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078958-T-G

149468918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50078962-T-C

149469174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50079202-T-G

http://identifiers.org/hco/2/GRCh38#149469528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50079507-C-A

149469543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50079522-A-G

149469689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50079683-C-T

149469708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50079701-T-C

http://identifiers.org/hco/2/GRCh38#149469898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50079907-C-A

149469943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50079946-A-G

149470226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50080234-G-A

149470258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 50080267-A-G

http://identifiers.org/hco/2/GRCh38#149470628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50080606-C-A

149470802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 50080781-G-A

149470823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 50080802-G-A

149470829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 50080808-G-A

149470900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50080881-T-A

149470946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50080928-G-A

149470965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50080947-G-A

149470965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50080947-G-T

149470966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50080948-G-A

149471017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50081003-T-C

http://identifiers.org/hco/2/GRCh38#149471039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50081025-C-A

149471039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50081025-C-T

149471057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50081055-T-C

149471102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 50081102-T-C

149471153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081150-G-A

149471153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081150-G-T

149471229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081218-G-T

149471275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081268-G-T

149471342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081335-C-G

149471432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081412-T-A

149471549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081534-G-T

149471908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081864-A-G

http://identifiers.org/hco/2/GRCh38#149471916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50081870-C-A

149471969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50081910-A-G

http://identifiers.org/hco/2/GRCh38#149472083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50082025-C-A

149472253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082210-G-T

149472377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082337-T-C

http://identifiers.org/hco/2/GRCh38#149472506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50082459-C-A

149472506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082459-C-T

149472619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082572-G-T

149472718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082665-C-T

149472847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082793-G-A

149472847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082793-G-C

149472857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50082822-G-A

http://identifiers.org/hco/2/GRCh38#149473189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50083145-C-A

149473189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083145-C-T

http://identifiers.org/hco/2/GRCh38#149473190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50083146-C-A

149473217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083173-A-G

149473217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083173-A-T

149473230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083186-T-C

149473292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083245-T-A

149473292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083245-T-C

149473292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083245-T-G

149473300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083253-G-A

149473380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083332-A-G

149473632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083579-A-G

http://identifiers.org/hco/2/GRCh38#149473674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50083617-C-A

149473674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083617-C-T

http://identifiers.org/hco/2/GRCh38#149473732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50083671-C-A

149473821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083739-G-A

149473887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50083801-G-A

149474107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50084029-T-C

http://identifiers.org/hco/2/GRCh38#149474140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50084060-C-A

149474171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 50084091-G-T

http://identifiers.org/hco/2/GRCh38#149475085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#50084334-C-A

149475085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 50084334-C-T

149475289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 50084549-C-T

149475660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 50085292-A-G

149475933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28751
most severe consequence: intron variant
orthologous variants: 50085548-A-G