24010118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense variant
orthologous variants: 4924313-G-A

http://identifiers.org/hco/2/GRCh38#24010136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4924300-C-A

24010136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: stop gained
orthologous variants: 4924300-C-T

http://identifiers.org/hco/2/GRCh38#24010174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4924263-C-A

24010174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: synonymous variant
orthologous variants: 4924263-C-T

24010443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4924056-T-C

24010542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4924009-C-T

24010663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4923889-C-T

24011347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4923251-G-A

24011347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4923251-G-C

http://identifiers.org/hco/2/GRCh38#24011592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4923013-C-A

24011685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4922917-T-C

24011746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4922867-A-T

24011783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: 4922847-C-T

http://identifiers.org/hco/2/GRCh38#24011831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4922808-C-A

24012911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4921826-T-G

24012945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4921792-G-C

24012945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4921792-G-T

24012993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4921783-A-T

24013049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4921729-G-T

http://identifiers.org/hco/2/GRCh38#24013129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4921649-C-A

24013167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921613-G-A

24013167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921613-G-T

24013234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921549-A-G

24013250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921533-T-C

24013257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921526-A-G

http://identifiers.org/hco/2/GRCh38#24013523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4921270-A-C

24013523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921270-A-G

http://identifiers.org/hco/2/GRCh38#24013545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4921247-C-A

24013545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4921247-C-T

24016036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920738-A-G

24016036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920738-A-T

24016112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920663-G-A

24016112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920663-G-C

24016112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920663-G-T

24016264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4920513-G-A

24016315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920462-C-T

http://identifiers.org/hco/2/GRCh38#24016368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4920424-C-A

24016368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920424-C-G

24016368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920424-C-T

24016395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4920398-G-T

http://identifiers.org/hco/2/GRCh38#24016691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4919796-C-A

24016785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919706-G-A

24016846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4919655-G-T

24016990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919510-G-T

24016991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919509-C-T

http://identifiers.org/hco/2/GRCh38#24017008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4919494-C-A

24017008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919494-C-G

24017089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919410-G-A

24017089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919410-G-T

http://identifiers.org/hco/2/GRCh38#24017213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4919291-C-A

24017213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919291-C-G

24017213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919291-C-T

24017257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919239-G-C

24017257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919239-G-T

24017258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919238-G-A

24017258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4919238-G-T

http://identifiers.org/hco/2/GRCh38#24017350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#4919144-C-A

24017350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4919144-C-T

24017450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4919049-G-A

24017450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4919049-G-T

24017586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4918913-G-A

24017586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4918913-G-C

24017586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4918913-G-T

24017688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4918829-T-C

24017699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4918818-G-A

24017699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4918818-G-T

24021226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4918105-T-C

24021450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917864-G-A

24021450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917864-G-C

24021504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917829-A-G

24021508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917825-G-A

24021508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917825-G-C

24021508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917825-G-T

http://identifiers.org/hco/2/GRCh38#24021524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917808-C-A

24021524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917808-C-T

http://identifiers.org/hco/2/GRCh38#24021527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917806-C-A

24021527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917806-C-G

http://identifiers.org/hco/2/GRCh38#24021528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917805-C-A

24021528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917805-C-G

24021528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917805-C-T

24021531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917802-G-A

24021531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917802-G-T

24021532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917801-G-A

24021532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917801-G-T

24021545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917784-C-T

http://identifiers.org/hco/2/GRCh38#24021615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917735-C-A

24021615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917735-C-T

http://identifiers.org/hco/2/GRCh38#24021627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917721-C-A

24021641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 4917707-C-T

24021673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4917675-C-T

24021696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4917652-G-A

24021733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4917615-G-A

24021740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 4917608-T-C

24021790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917554-G-A

24021794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917550-G-A

24021794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917550-G-C

24021953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4917353-A-G

24021974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917332-C-T

24022026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917284-T-C

24022045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917255-T-C

http://identifiers.org/hco/2/GRCh38#24022097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4917145-C-A

24022097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917145-C-G

24022210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4917059-T-C

24022381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916923-T-G

http://identifiers.org/hco/2/GRCh38#24022387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916917-C-A

24022387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916917-C-G

24022387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916917-C-T

24022397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916907-G-T

24022553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916749-G-T

24022627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916704-G-C

24022627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916704-G-T

24022660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916681-G-A

24022660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916681-G-C

24022660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916681-G-T

24022734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916611-G-T

http://identifiers.org/hco/2/GRCh38#24022741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916604-A-C

24022741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916604-A-G

24022741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916604-A-T

24022742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916603-A-G

http://identifiers.org/hco/2/GRCh38#24022766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916579-C-A

24022766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916579-C-T

http://identifiers.org/hco/2/GRCh38#24022780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916569-C-A

24022780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916569-C-G

24022780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4916569-C-T

http://identifiers.org/hco/2/GRCh38#24023081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916309-C-A

24023081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4916309-C-T

24023208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4916188-G-A

24023259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916122-C-T

24023260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916121-T-C

24023277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916105-G-A

24023277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916105-G-T

24023279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916103-G-T

http://identifiers.org/hco/2/GRCh38#24023370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4916043-C-A

24023370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916043-C-T

24023395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 4916019-G-T

24023692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915760-G-A

24023692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915760-G-C

24023692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915760-G-T

24023695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915757-T-C

24023695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915757-T-G

http://identifiers.org/hco/2/GRCh38#24023830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4915626-C-A

24023830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915626-C-T

24023837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915619-G-A

24023837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915619-G-T

24023856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915602-G-A

24023867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915591-T-G

http://identifiers.org/hco/2/GRCh38#24023868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4915590-C-A

24023868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915590-C-T

http://identifiers.org/hco/2/GRCh38#24023869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4915589-C-A

24023869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915589-C-T

24023873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915585-G-T

http://identifiers.org/hco/2/GRCh38#24023959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4915445-A-C

24024011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915398-G-A

24024011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4915398-G-T

24024249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915157-T-A

24024249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4915157-T-C

24024273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 4915133-T-C

24024361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4914998-G-A

24024361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4914998-G-T

24024438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914928-T-C

24024671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914774-C-T

24024750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914699-C-T

24024772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914678-G-A

24024897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914556-A-T

24025245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914245-G-T

http://identifiers.org/hco/2/GRCh38#24025334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4914171-A-C

24025357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914148-C-T

24025377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4914128-A-G

http://identifiers.org/hco/2/GRCh38#24029202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4910019-A-C

24029218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4910002-T-C

24029226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4909992-G-A

24029248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4909974-G-A

24029248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4909974-G-T

24029365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909889-T-A

24029365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909889-T-C

http://identifiers.org/hco/2/GRCh38#24029532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909715-A-C

24029569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909677-G-A

24029569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909677-G-T

http://identifiers.org/hco/2/GRCh38#24029585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909660-C-A

24029585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909660-C-T

24029592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909651-C-T

http://identifiers.org/hco/2/GRCh38#24029595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909648-C-A

http://identifiers.org/hco/2/GRCh38#24029630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909613-C-A

24029632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909611-C-T

24029704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909540-A-G

24029728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909516-G-A

24029728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909516-G-T

http://identifiers.org/hco/2/GRCh38#24029802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909445-C-A

24029802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4909445-C-T

http://identifiers.org/hco/2/GRCh38#24029813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4909426-C-A

24030146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908858-A-G

24030216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908783-G-A

24030216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908783-G-C

24030254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908771-A-G

http://identifiers.org/hco/2/GRCh38#24030255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908770-C-A

24030255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908770-C-T

http://identifiers.org/hco/2/GRCh38#24030326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908704-C-A

http://identifiers.org/hco/2/GRCh38#24030349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908681-A-C

24030379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908647-G-T

24030510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908341-G-A

24030510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908341-G-T

24030554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908291-A-G

http://identifiers.org/hco/2/GRCh38#24030576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908269-C-A

24030576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908269-C-T

24030606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908225-C-T

http://identifiers.org/hco/2/GRCh38#24030653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908173-C-A

24030653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908173-C-T

http://identifiers.org/hco/2/GRCh38#24030736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908105-C-A

24030752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908101-A-G

24030752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908101-A-T

24030763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908090-A-G

24030786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908088-G-T

24030914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4908033-A-G

http://identifiers.org/hco/2/GRCh38#24030960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4908007-A-C

http://identifiers.org/hco/2/GRCh38#24031025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4907942-C-A

24031025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4907942-C-G

24031025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4907942-C-T

24031063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4907904-C-T

24031096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4907871-T-G

24031201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4907765-A-G

24032795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4905409-T-A

24032795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4905409-T-G

http://identifiers.org/hco/2/GRCh38#24032824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4905395-C-A

24032824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4905395-C-T

24032828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 4905391-C-T

24037542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4902064-T-C

http://identifiers.org/hco/2/GRCh38#24037597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4902025-C-A

24037605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4902011-T-G

24037617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4901999-A-G

24037631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4901985-G-T

24037683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4901934-A-G

24037709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 4901908-G-A

24037709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901908-G-C

24037720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901897-T-A

24037731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4901886-G-A

24037731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4901886-G-C

24037732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901885-G-A

24037732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901885-G-C

24037734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4901883-T-C

24037745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901872-T-C

http://identifiers.org/hco/2/GRCh38#24037750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4901867-A-C

24037750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901867-A-G

24037832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901785-A-G

24037832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901785-A-T

24037868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901749-G-A

24038049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4901565-A-G

24038152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901462-T-G

24038533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4901081-A-G

24038713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900904-T-A

24038713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900904-T-C

24038766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4900872-A-G

http://identifiers.org/hco/2/GRCh38#24039135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4900503-C-A

24039135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4900503-C-T

24039139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900499-C-T

24039188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900450-A-T

24039245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900393-G-T

http://identifiers.org/hco/2/GRCh38#24039271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4900367-A-C

24039274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900364-G-A

24039279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 4900359-A-G

24039281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900357-C-T

24039395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 4900243-C-T

http://identifiers.org/hco/2/GRCh38#24047098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4893600-C-A

24047128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4893574-C-G

24047192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4893517-T-C

http://identifiers.org/hco/2/GRCh38#24047341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4893413-C-A

24047341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4893413-C-T

24047373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4893391-G-A

24047373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4893391-G-T

24047380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 4893384-A-G

24047414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4893350-C-T

24047538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4893290-G-A

http://identifiers.org/hco/2/GRCh38#24047731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4892910-C-A

24047934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4892664-G-C

24047979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4892622-C-T

24048061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4892545-C-T

24049053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891972-T-C

http://identifiers.org/hco/2/GRCh38#24049076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4891949-C-A

24049100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891923-T-C

http://identifiers.org/hco/2/GRCh38#24049120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4891903-C-A

http://identifiers.org/hco/2/GRCh38#24049538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4891766-A-C

24049538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891766-A-G

24049538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891766-A-T

24049626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891659-C-G

24049626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891659-C-T

24049652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 4891633-A-T

24049867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4891416-G-A

24049867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4891416-G-T

24049950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4891338-G-A

24049992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4891297-G-A

24049992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4891297-G-T

http://identifiers.org/hco/2/GRCh38#24050006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4891280-A-C

24050006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4891280-A-G

http://identifiers.org/hco/2/GRCh38#24050022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4891263-C-A

24050022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4891263-C-T

24050431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4890879-T-A

24050435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4890875-C-T

24050730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4890563-T-C

24050756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4890537-A-G

24051465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4890187-G-A

24052038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889564-A-G

24052047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889561-C-T

24052105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889502-A-G

24052136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889470-T-C

24052223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889392-C-T

24052422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889206-C-G

24052490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889155-C-T

http://identifiers.org/hco/2/GRCh38#24052509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4889137-C-A

24052640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4889010-T-A

24053478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4888698-G-A

24053533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4888648-A-G

24053735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4888464-G-A

24053974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4888142-A-G

http://identifiers.org/hco/2/GRCh38#24053990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4888126-C-A

24053990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4888126-C-G

24053990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4888126-C-T

24054032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4888085-T-C

24054073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4888053-C-T

http://identifiers.org/hco/2/GRCh38#24054074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4888052-C-A

24054098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4888033-T-C

24054159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4888027-A-G

24054195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4887991-G-A

24054195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4887991-G-T

http://identifiers.org/hco/2/GRCh38#24054493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4887483-C-A

24054764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4887207-T-C

24054839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4887132-G-A

24058338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4886228-G-A

24058658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4885928-A-T

24058957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4885635-C-G

http://identifiers.org/hco/2/GRCh38#24059849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4885410-C-A

24059849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4885410-C-T

24059907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4885368-A-T

24060698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884961-G-C

24060698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884961-G-T

24060720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884941-T-A

24060767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884896-T-C

24060780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884883-A-G

http://identifiers.org/hco/2/GRCh38#24060819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4884844-C-A

24060819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4884844-C-T

24060974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884675-G-T

http://identifiers.org/hco/2/GRCh38#24061061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4884633-A-C

24061061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4884633-A-G

http://identifiers.org/hco/2/GRCh38#24061072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4884623-C-A

24061072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884623-C-T

24061078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884617-G-C

24061078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884617-G-T

24061168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4884552-A-G

http://identifiers.org/hco/2/GRCh38#24063216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4883641-C-A

24063216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883641-C-T

24063223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883634-T-C

http://identifiers.org/hco/2/GRCh38#24063226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4883631-C-A

24063226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883631-C-T

http://identifiers.org/hco/2/GRCh38#24063305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4883549-C-A

24063305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883549-C-G

24063312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883542-A-G

24063312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37207
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 4883542-A-T