21901076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842287-C-G

21901076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842287-C-T

21901094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842269-C-G

21901129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842234-T-C

21901138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842225-C-T

21901228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842135-G-A

21901228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117842135-G-C

21901265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842087-G-C

21901296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842057-A-G

21901401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841991-A-G

http://identifiers.org/hco/7/GRCh38#21901423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841969-C-A

21901423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841969-C-G

http://identifiers.org/hco/7/GRCh38#21901443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841966-C-A

21901443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841966-C-G

21901443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841966-C-T

http://identifiers.org/hco/7/GRCh38#21901484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841941-A-C

21901484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841941-A-G

21901484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841941-A-T

http://identifiers.org/hco/7/GRCh38#21901680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841831-C-A

21901692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841822-T-A

21901692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841822-T-C

http://identifiers.org/hco/7/GRCh38#21901775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841744-A-C

21901775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841744-A-T

21901853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841665-A-G

http://identifiers.org/hco/7/GRCh38#21901952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841554-C-A

21901952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841554-C-G

21901952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841554-C-T

21901960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841546-G-A

21901960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841546-G-T

21901965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841541-C-T

21901975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841540-T-C

21901975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841540-T-G

21902061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841459-T-G

21902151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841381-C-T

21902269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841277-A-T

21902278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117841268-T-C

21902438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841117-G-C

21902438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841117-G-T

http://identifiers.org/hco/7/GRCh38#21902532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841092-C-A

21902532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841092-C-G

21902538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117841086-T-C

http://identifiers.org/hco/7/GRCh38#21902542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#117841082-C-A

21902542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117841082-C-T

21902559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841065-G-A

21902559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841065-G-C

21902559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841065-G-T

21902633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841010-T-A

21902633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117841010-T-C

21902674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840976-G-A

21902674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840976-G-T

21902742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840941-T-C

21902742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840941-T-G

http://identifiers.org/hco/7/GRCh38#21902797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117840889-C-A

21902797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840889-C-G

21902797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840889-C-T

21902923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840804-T-C

21902924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840803-G-A

21902924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117840803-G-T

21903058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117840695-A-T

http://identifiers.org/hco/7/GRCh38#21903133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117840620-C-A

21903133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840620-C-T

21903158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840589-G-T

http://identifiers.org/hco/7/GRCh38#21903202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117840520-C-A

21903202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840520-C-T

21903571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840099-T-C

21903610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840067-G-A

21903610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840067-G-T

http://identifiers.org/hco/7/GRCh38#21903615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117840060-C-A

21903615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840060-C-G

21903657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840003-G-A

21903657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117840003-G-T

21903666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839994-C-G

21903666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839994-C-T

21903672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839988-T-A

21903672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839988-T-G

21903692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839968-T-A

21903692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839968-T-G

21903705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839921-G-A

http://identifiers.org/hco/7/GRCh38#21903713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839895-C-A

21903713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839895-C-G

21903713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839895-C-T

21903960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839591-T-C

http://identifiers.org/hco/7/GRCh38#21904000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839548-A-C

http://identifiers.org/hco/7/GRCh38#21904037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839515-C-A

21904037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839515-C-T

http://identifiers.org/hco/7/GRCh38#21904059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839508-C-A

21904059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839508-C-G

21904059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839508-C-T

http://identifiers.org/hco/7/GRCh38#21904079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839489-A-C

21904084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839484-A-G

21904100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839468-C-G

21904100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117839468-C-T

http://identifiers.org/hco/7/GRCh38#21904105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839463-C-A

21904144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117839423-T-A

http://identifiers.org/hco/7/GRCh38#21904159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839408-C-A

21904159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117839408-C-T

http://identifiers.org/hco/7/GRCh38#21904209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117839358-C-A

21904243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117839324-T-C

21904861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839107-G-A

21904861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117839107-G-C

21905010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838979-A-T

21905230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838765-C-T

21905310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838727-G-A

http://identifiers.org/hco/7/GRCh38#21905359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117838676-A-C

21905359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838676-A-G

21905485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838576-G-A

21905485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838576-G-T

http://identifiers.org/hco/7/GRCh38#21905600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117838445-C-A

21905600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117838445-C-T

21905643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117838405-A-G

21905670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117838378-A-G

http://identifiers.org/hco/7/GRCh38#21905745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117838302-C-A

21905745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838302-C-G

21905788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838278-T-A

21905788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838278-T-C

21905795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838271-T-A

21905795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838271-T-C

21905795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838271-T-G

21905820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838249-G-A

21905820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838249-G-C

21905991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117838116-T-C

21906194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837879-G-A

21906194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837879-G-T

http://identifiers.org/hco/7/GRCh38#21906231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117837834-A-C

http://identifiers.org/hco/7/GRCh38#21906279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117837809-C-A

21906386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117837699-G-A

21906407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117837678-C-G

21906407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117837678-C-T

21906466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837619-A-G

21906467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837618-G-C

21906476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837609-C-G

21906549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837544-T-C

21906685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837402-A-G

21906685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837402-A-T

21906692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837395-G-A

21906692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837395-G-T

21906759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837359-A-G

21906759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117837359-A-T

21907695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117836498-G-C

21907875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117836332-T-A

21907951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117836278-T-A

21907951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117836278-T-C

21908245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117836055-A-G

21908276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117836024-T-C

21908276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117836024-T-G

http://identifiers.org/hco/7/GRCh38#21908459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#117835868-C-A

21908459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117835868-C-T

21908466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117835861-C-G

21908467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117835860-A-G

21908531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117835793-A-G

21910494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117835183-C-T

21910724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117834354-G-C

21910797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117834283-C-G

21910797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117834283-C-T

21910850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117834239-G-A

21911851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833678-T-A

21911860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833669-T-C

21911860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833669-T-G

21911861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833668-G-A

21911861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833668-G-T

21911874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833654-G-A

21911874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833654-G-T

21912020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833557-G-A

21912118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833420-T-G

21912125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833413-G-C

21912219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833288-A-G

21912219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833288-A-T

21912365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832963-T-G

21912500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832851-A-G

http://identifiers.org/hco/7/GRCh38#21912542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117832831-C-A

21912561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832814-A-T

21912725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832652-G-A

21912948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832438-G-C

21913049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832364-T-C

http://identifiers.org/hco/7/GRCh38#21913097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117832317-C-A

21913097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832317-C-T

21913153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832261-G-A

21913524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831732-A-G

21913905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831409-T-C

21913905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831409-T-G

21914103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831249-G-A

21914126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831223-C-T

21914164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831188-C-T

21914167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831186-T-C

21914332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831053-T-C

21914535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830933-A-G

21914650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830877-G-A

21914669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830860-A-G

21914787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830763-A-G

21914848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830675-T-C

21914975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830583-G-C

21915032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830534-T-A

21915147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830431-G-T

21915217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830363-A-T

http://identifiers.org/hco/7/GRCh38#21915347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117830200-A-C

21915396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830134-A-G

http://identifiers.org/hco/7/GRCh38#21915483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829980-A-C

21915516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829946-G-A

21915564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829891-A-G

http://identifiers.org/hco/7/GRCh38#21915572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829883-C-A

21915611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829849-A-G

http://identifiers.org/hco/7/GRCh38#21915621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829839-A-C

http://identifiers.org/hco/7/GRCh38#21915666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829787-C-A

21915946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829518-G-A

21915987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829488-G-C

21916066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829443-C-G

http://identifiers.org/hco/7/GRCh38#21916215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829340-C-A

http://identifiers.org/hco/7/GRCh38#21916355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829213-C-A

21916355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829213-C-T

21916426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829161-G-A

http://identifiers.org/hco/7/GRCh38#21916505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829108-C-A

21916544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829095-A-G

21916544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829095-A-T

http://identifiers.org/hco/7/GRCh38#21916632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117829023-A-C

21916664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828992-C-T

21916677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828979-T-A

21916677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828979-T-C

21916695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828961-T-C

http://identifiers.org/hco/7/GRCh38#21916730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117828922-C-A

21916730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828922-C-G

http://identifiers.org/hco/7/GRCh38#21916789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117828862-A-C

21916823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117828834-A-G

21916848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117828809-T-G

http://identifiers.org/hco/7/GRCh38#21916864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117828793-C-A

21916864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117828793-C-T

http://identifiers.org/hco/7/GRCh38#21917019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117828706-C-A

21917034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828691-A-G

21917138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828591-A-G

21917352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828419-A-G

21917361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828410-C-T

21917476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828295-A-G

21917502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117828272-T-C

21920837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117827402-T-A

http://identifiers.org/hco/7/GRCh38#21921140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117826687-C-A

21924214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117823588-G-T

21924434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117823399-G-C

21924434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117823399-G-T

21924576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117822892-C-G

21924576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117822892-C-T

21939394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815972-G-A

21939530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117815829-G-T

21939632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815738-T-C

21939815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117815646-C-T

http://identifiers.org/hco/7/GRCh38#21939949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117815542-C-A

21940025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815499-G-A

21940121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815425-G-A

21940121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815425-G-T

http://identifiers.org/hco/7/GRCh38#21940191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117815349-C-A

21940213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815327-T-C

21940213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815327-T-G

21940220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815319-G-T

21940287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117815249-T-C

http://identifiers.org/hco/7/GRCh38#21940303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117815233-C-A

21940303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117815233-C-T

21940342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815191-T-C

21940343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815190-G-T

21940354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815186-G-C

21940354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117815186-G-T

21941289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117811571-A-G

21941813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810688-T-A

21941848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810655-T-A

21941848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810655-T-G

21941892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810633-A-G

21942085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810515-A-G

21942147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810489-T-C

21942178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810468-G-A

21942271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810396-A-G

http://identifiers.org/hco/7/GRCh38#21942388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117810297-A-C

21942440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117810255-A-T

http://identifiers.org/hco/7/GRCh38#21942632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117810122-A-C

21943355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809736-T-C

21943386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809702-C-T

21943888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809258-C-T

21943897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809249-C-G

21944054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809140-C-T

21944227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809036-T-A

21944227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117809036-T-C

21944309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808986-G-A

http://identifiers.org/hco/7/GRCh38#21944529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117808787-A-C

21944640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808717-A-G

21944641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808716-G-A

21944641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808716-G-T

21944664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808693-A-G

21944664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808693-A-T

21944680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117808677-T-C

21944699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117808626-G-A

21944700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117808625-C-T

http://identifiers.org/hco/7/GRCh38#21944701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117808624-C-A

http://identifiers.org/hco/7/GRCh38#21944811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117808552-A-C

21944836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117808546-T-G

http://identifiers.org/hco/7/GRCh38#21944887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117808530-A-C

21944927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808492-C-T

21945013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808411-C-T

http://identifiers.org/hco/7/GRCh38#21945022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#117808402-C-A

21945160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808241-G-C

21945299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117808115-A-T

21945518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807882-G-A

21945567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117807853-G-T

http://identifiers.org/hco/7/GRCh38#21945667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#117807789-C-A

21945667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807789-C-G

http://identifiers.org/hco/7/GRCh38#21945702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#117807763-C-A

21945702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807763-C-G

21945702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807763-C-T

21945713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117807752-G-A

21945713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron variant
orthologous variants: 117807752-G-T

21945720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807745-G-A

21945720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807745-G-C

21945720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30777
most severe consequence: intron_variant, undefined
orthologous variants: 117807745-G-T