150000089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61310554-G-A

150000286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61310436-A-G

150000301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 61310421-A-G

http://identifiers.org/hco/5/GRCh38#150000311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61310411-C-A

150000311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 61310411-C-T

http://identifiers.org/hco/5/GRCh38#150000449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61310368-C-A

http://identifiers.org/hco/5/GRCh38#150000505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61310313-A-C

150000505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61310313-A-G

http://identifiers.org/hco/5/GRCh38#150000510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61310308-C-A

150000510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61310308-C-G

150000510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61310308-C-T

http://identifiers.org/hco/5/GRCh38#150000527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61310291-C-A

150000527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61310291-C-T

150001192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61309634-T-C

150001199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61309619-G-A

http://identifiers.org/hco/5/GRCh38#150001235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61309582-C-A

150001235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61309582-C-T

http://identifiers.org/hco/5/GRCh38#150001266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61309546-C-A

150001423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61309486-A-G

150001481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61309428-A-G

150002152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61308539-C-G

150002152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61308539-C-T

150002492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61307339-T-C

http://identifiers.org/hco/5/GRCh38#150002498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61307323-C-A

150002502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61307319-A-G

150004445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61305700-G-C

150004652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61305528-C-G

150005024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61305186-A-G

150006665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61304262-C-T

150006762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61304165-T-G

150006977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61303964-T-C

http://identifiers.org/hco/5/GRCh38#150007429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61303494-A-C

150007572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61303350-T-C

150007650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61303274-C-G

150007676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61303252-A-G

150008882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61302033-A-G

150009048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301874-G-T

150009062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301860-T-A

150009142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301786-C-T

http://identifiers.org/hco/5/GRCh38#150009150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61301770-A-C

150009431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301509-T-C

150009463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301477-A-G

150009493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301444-G-A

150009711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61301244-A-G

150009983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61300880-G-C

150010007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61300849-G-A

150010007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61300849-G-C

http://identifiers.org/hco/5/GRCh38#150010049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61300821-C-A

150010171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, missense_variant
orthologous variants: 61300703-C-T

150010226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, missense_variant
orthologous variants: 61300648-G-A

150010226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, missense_variant
orthologous variants: 61300648-G-T

150010293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61300581-C-T

150010354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, missense_variant
orthologous variants: 61300520-G-A

150010531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, missense_variant
orthologous variants: 61300343-C-T

150010536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 61300338-C-T

150010763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61299934-G-A

150010909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61299812-C-G

150011501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61299260-C-T

http://identifiers.org/hco/5/GRCh38#150011916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61298939-C-A

150012074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61298828-A-G

150012273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61298635-T-C

150018733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61295941-C-G

150021375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61292703-A-G

http://identifiers.org/hco/5/GRCh38#150021387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61292691-A-C

150022302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61292550-T-G

150023582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61291464-T-C

150024083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290999-G-A

150024119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290965-T-G

150024148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290945-A-G

150024166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290928-A-G

150024725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290346-A-G

150024830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290251-A-G

150025054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61290004-A-G

150025083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61289980-G-A

150025262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61289800-C-G

150026120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61289024-G-A

150026176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61288978-G-A

150026176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61288978-G-C

150026187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61288967-A-G

150026187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61288967-A-T

150026294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, undefined
orthologous variants: 61288928-A-G

150026413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288835-G-C

150026442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288806-A-G

http://identifiers.org/hco/5/GRCh38#150026628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61288592-A-C

150026628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288592-A-G

150026837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, undefined
orthologous variants: 61288371-G-A

150026837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, undefined
orthologous variants: 61288371-G-T

150026839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, undefined
orthologous variants: 61288369-A-G

150026840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, undefined
orthologous variants: 61288368-G-T

150026897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288314-T-C

150026913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288300-G-A

150026913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288300-G-T

150026924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288289-G-A

150027007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61288208-C-T

http://identifiers.org/hco/5/GRCh38#150027267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61287968-A-C

150027267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61287968-A-G

150027267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61287968-A-T

http://identifiers.org/hco/5/GRCh38#150027285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61287953-A-C

150027418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61287829-C-T

150029698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61286126-G-A

150029698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61286126-G-T

150030104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61285803-T-G

150030160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61285760-A-G

http://identifiers.org/hco/5/GRCh38#150030430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61285637-C-A

150030532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285562-G-A

150030532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285562-G-T

150030537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285557-G-T

http://identifiers.org/hco/5/GRCh38#150030548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61285548-C-A

150030548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285548-C-T

150030556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285540-G-A

150030556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285540-G-T

150030567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285529-T-C

150030569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285527-A-T

http://identifiers.org/hco/5/GRCh38#150030607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61285489-A-C

150030614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285483-A-G

150030625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285472-G-T

150030628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285469-G-A

150030641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285454-A-G

150030681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285416-T-A

150030681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285416-T-C

150030681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61285416-T-G

150030801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61285293-A-G

150030885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61285219-T-C

150030909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61285196-G-T

150030922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61285183-G-A

150030922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61285183-G-T

150030927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61285178-T-G

150031107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61284981-A-T

http://identifiers.org/hco/5/GRCh38#150032402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61283645-C-A

150032402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61283645-C-T

150032655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61283397-T-G

http://identifiers.org/hco/5/GRCh38#150032711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61283358-C-A

http://identifiers.org/hco/5/GRCh38#150032723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61283348-A-C

150032723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61283348-A-T

150032756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61283318-C-T

150036780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61280474-T-C

150036985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61280295-C-G

http://identifiers.org/hco/5/GRCh38#150037010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61280271-A-C

150037010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61280271-A-G

150037067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61280213-T-G

150037120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279926-G-A

150037212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279828-T-C

http://identifiers.org/hco/5/GRCh38#150037268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61279766-A-C

150037268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279766-A-G

150037555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279472-A-G

150037589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279439-G-A

150037589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279439-G-T

150037651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279382-A-G

150037670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61279363-T-C

150040682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61274921-T-G

150040716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61274888-T-C

http://identifiers.org/hco/5/GRCh38#150040742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61274866-C-A

150040742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61274866-C-T

150041209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61274499-C-T

150041315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61274392-T-C

150041322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61274385-T-G

150041500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61274239-G-A

150041564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61274168-T-A

150045255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270937-G-T

150045449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270715-T-C

150045449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270715-T-G

150045711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270447-G-A

150045711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270447-G-T

150045754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270407-G-A

http://identifiers.org/hco/5/GRCh38#150045763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61270401-C-A

150045763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61270401-C-T

http://identifiers.org/hco/5/GRCh38#150047370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61269696-C-A

150047370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269696-C-G

150047372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269694-G-A

150047372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269694-G-T

http://identifiers.org/hco/5/GRCh38#150047412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61269657-A-C

150047412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269657-A-G

150047412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269657-A-T

150047459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269584-A-G

150047459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 61269584-A-T

150047485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269553-A-G

150047565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269483-G-A

150047565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269483-G-C

150047584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269469-G-A

150047600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269454-C-T

150047608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61269446-C-G

http://identifiers.org/hco/5/GRCh38#150047692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61269362-A-C

150047692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61269362-A-G

150047788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269272-G-A

150047811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269249-T-C

http://identifiers.org/hco/5/GRCh38#150047812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61269248-C-A

150047812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269248-C-T

http://identifiers.org/hco/5/GRCh38#150047836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61269227-A-C

150047836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269227-A-G

150047857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269203-T-A

150047857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269203-T-C

150048040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269094-T-G

150048146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61269006-A-G

150048410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268788-G-A

150048410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268788-G-T

150048420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268778-G-A

http://identifiers.org/hco/5/GRCh38#150048438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61268763-C-A

150048461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268752-G-A

150048461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268752-G-T

150048486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268729-T-C

150048491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268724-T-C

150048526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268700-T-C

150048548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268678-A-T

150048587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 61268639-T-C

150048587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61268639-T-G

150048705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268533-G-T

150048789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268453-G-A

150049115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268231-C-T

150049171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268201-G-A

150049171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268201-G-T

150049239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268170-C-T

150049387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268076-C-T

150049407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61268056-G-C

150049585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61267933-C-G

150049610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61267909-G-A

150049888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61267693-C-T

150050108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61267535-A-G

150050115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61267528-G-T

150050247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61267138-C-T

150050384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61266999-C-T

150050445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61266938-C-T

150050817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266757-G-C

150050997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266452-A-G

150051060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266271-T-C

150051128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266202-G-T

http://identifiers.org/hco/5/GRCh38#150051134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61266196-A-C

150051148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266182-G-C

150051148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266182-G-T

150051262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266075-A-G

150051319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61266022-C-T

150051370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265983-C-T

150051600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265781-A-G

150051604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265777-A-G

150051631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265750-A-G

150051631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265750-A-T

150051660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265728-G-A

150051660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265728-G-T

150051712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: intron variant
orthologous variants: 61265678-A-G

150051785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265605-C-T

http://identifiers.org/hco/5/GRCh38#150051816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61265574-C-A

150051816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265574-C-T

150051828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265562-T-C

150052154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265248-G-A

150052154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265248-G-C

150052172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: missense variant
orthologous variants: 61265230-G-A

150052249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265149-T-C

150052250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265148-G-A

150052250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265148-G-T

150052255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265143-A-G

150052297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265108-G-A

150052297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61265108-G-T

150052431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264990-G-A

150052431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264990-G-C

150052431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264990-G-T

150052467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264951-G-A

150052467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264951-G-T

150052564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264891-A-G

http://identifiers.org/hco/5/GRCh38#150052586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61264867-C-A

150052586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264867-C-T

150052618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264844-T-C

150052618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264844-T-G

150052746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264729-C-G

150052746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264729-C-T

http://identifiers.org/hco/5/GRCh38#150052809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61264682-C-A

http://identifiers.org/hco/5/GRCh38#150052812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61264679-C-A

150052812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264679-C-T

150052966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264529-A-G

150052998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: 61264497-C-T

http://identifiers.org/hco/5/GRCh38#150053020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28982
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61264475-C-A