http://identifiers.org/hco/4/GRCh38#73431168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90632695-C-A

73431225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: non coding transcript exon variant
orthologous variants: 90632736-G-T

73431302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90632807-A-G

73431488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90632963-A-G

73431582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90633018-T-C

73432046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90633455-T-A

73432202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90633603-T-A

73433351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90635821-A-G

73433445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90635910-C-T

73433456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90635921-T-C

73433590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636056-T-C

http://identifiers.org/hco/4/GRCh38#73433607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90636073-A-C

http://identifiers.org/hco/4/GRCh38#73433812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90636503-A-C

73433915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636577-C-T

73433959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636622-G-T

73434007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636669-T-C

73434029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636680-T-C

73434110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90636748-G-C

73435006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90637237-C-T

73435116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90637336-G-A

73435149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90637369-C-T

http://identifiers.org/hco/4/GRCh38#73435276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90637742-A-C

73435589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638100-T-A

73435699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638174-A-G

73435955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638356-C-G

73436178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638552-T-C

http://identifiers.org/hco/4/GRCh38#73436230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90638607-C-A

73436230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90638607-C-T

73436276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90638653-A-G

73436313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90638690-A-G

73436313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90638690-A-T

73436328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90638705-T-A

73436328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90638705-T-G

73436360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638737-G-A

73436360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638737-G-T

http://identifiers.org/hco/4/GRCh38#73436382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90638759-A-C

73436382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638759-A-G

http://identifiers.org/hco/4/GRCh38#73436389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90638766-A-C

73436389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638766-A-G

73436411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638789-G-A

73436411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90638789-G-T

73436514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639060-C-T

73436895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639332-G-C

73437046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639463-T-C

73437049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639466-A-G

73437049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639466-A-T

73437057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639474-A-G

73437113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639516-T-A

73437113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639516-T-C

73437114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639517-G-T

73437118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639521-G-A

73437118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90639521-G-T

73437292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90639675-T-A

73437292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90639675-T-G

73437538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90639912-T-C

73437715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640080-A-T

73437727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640092-G-C

73437872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640234-T-C

73437872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640234-T-G

73437964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640321-T-C

73438036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640392-C-G

73438036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640392-C-T

http://identifiers.org/hco/4/GRCh38#73438069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90640429-A-C

73438125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640459-G-A

73438125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640459-G-C

73438126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640460-C-T

73438149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640484-G-A

73438149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640484-G-T

73438150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640485-G-C

73438150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640485-G-T

73438288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 90640611-A-G

73438333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640654-T-C

73438333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640654-T-G

73438401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640710-T-A

73438454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640765-A-G

73438652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640959-G-A

http://identifiers.org/hco/4/GRCh38#73438683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90640988-A-C

73438683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90640988-A-G

73438721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90641026-T-C

73438762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90641058-C-T

73439784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643337-C-T

73440375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643562-T-G

73440448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643673-T-C

73440496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643719-A-G

73440496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643719-A-T

http://identifiers.org/hco/4/GRCh38#73440520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90643743-C-A

73440587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643804-A-G

73440587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643804-A-T

73440589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90643806-A-T

http://identifiers.org/hco/4/GRCh38#73440628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#90643849-C-A

73440628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 90643849-C-T

73440685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90643906-A-G

73440685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, missense_variant
orthologous variants: 90643906-A-T

73440755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, missense_variant
orthologous variants: 90643976-C-T

73440782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, missense_variant
orthologous variants: 90644003-T-C

73440799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 90644020-G-A

http://identifiers.org/hco/4/GRCh38#73440909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90644113-A-C

73440909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644113-A-G

http://identifiers.org/hco/4/GRCh38#73440912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90644116-A-C

73440916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644120-A-G

73441048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644218-A-G

73441916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644690-A-G

73442147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644897-T-C

http://identifiers.org/hco/4/GRCh38#73442176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90644925-C-A

73442203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644960-G-A

73442203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90644960-G-T

73442357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90645117-G-A

73442434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90645194-A-G

http://identifiers.org/hco/4/GRCh38#73442484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90645247-C-A

73442485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90645248-A-G

73443205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90645993-T-A

73443404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90646181-G-A

73443460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646234-A-G

http://identifiers.org/hco/4/GRCh38#73443511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90646256-C-A

73443511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646256-C-G

73443511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646256-C-T

73443519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646264-T-A

73443519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646264-T-C

73443522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646267-T-C

73443533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646278-T-G

73443572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646303-G-T

http://identifiers.org/hco/4/GRCh38#73443595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90646326-C-A

73443595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646326-C-G

73443730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646454-C-T

73443825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646549-C-T

73443894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646611-C-T

73443931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646648-T-C

73444178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646763-C-G

73444325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646907-A-G

73444343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646928-G-A

73444343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646928-G-T

73444409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90646987-A-G

73444705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647178-A-G

73444808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647285-A-G

73444809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647286-G-C

73444843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647318-G-A

73444843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647318-G-T

http://identifiers.org/hco/4/GRCh38#73444860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90647335-C-A

73444860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647335-C-T

http://identifiers.org/hco/4/GRCh38#73444874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90647349-C-A

73444876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647351-A-G

73444973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647442-A-G

73445021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90647487-A-G

73445071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90647537-T-A

73445071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: synonymous variant
orthologous variants: 90647537-T-C

73445071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90647537-T-G

73445196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647623-G-A

73445212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647646-G-A

73445338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647761-G-T

73445585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647908-C-G

73445660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90647983-A-G

http://identifiers.org/hco/4/GRCh38#73445867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90648162-C-A

73446099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90648365-G-A

73446400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90648668-A-T

73446529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90648768-C-G

73446529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90648768-C-T

73446562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, undefined
orthologous variants: 90648799-T-A

73446805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, undefined
orthologous variants: 90648938-T-C

73446921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649028-G-C

73447095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650302-A-G

73447361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649144-T-A

73447361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649144-T-C

73447361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649144-T-G

73447441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649206-A-G

73447441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649206-A-T

73447593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: synonymous variant
orthologous variants: 90649397-T-C

73447722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649526-T-C

73447751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649532-G-A

73447751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649532-G-T

73447763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649544-T-C

73447862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649638-T-G

73447961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649744-T-C

73447962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649745-C-T

73447974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90649757-A-G

73448221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650159-A-G

73448231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650169-T-G

73448762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650710-T-A

73448956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650897-C-G

http://identifiers.org/hco/4/GRCh38#73448985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90650918-C-A

73449059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90650984-T-C

73449181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651271-C-T

73449188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651278-T-A

73449188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651278-T-C

73449306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651407-C-G

http://identifiers.org/hco/4/GRCh38#73449322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90651420-C-A

73449322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651420-C-G

73449362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: synonymous variant
orthologous variants: 90651460-T-C

73449404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: synonymous variant
orthologous variants: 90651502-A-T

73449764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90651988-T-G

73449905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652060-C-T

73449985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652138-T-C

73449999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652152-A-G

73450002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652155-G-A

73450078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense variant
orthologous variants: 90652232-G-T

http://identifiers.org/hco/4/GRCh38#73450147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90652301-A-C

73450170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652323-A-G

73450217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652464-A-G

73450293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652540-A-G

73450310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652558-G-A

73450341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652589-A-G

73450358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652606-C-T

http://identifiers.org/hco/4/GRCh38#73450511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#90652722-C-A

73450511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, undefined
orthologous variants: 90652722-C-T

73450540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652749-T-A

73450540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron variant
orthologous variants: 90652749-T-C

73450573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90652780-T-C

73450573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90652780-T-G

http://identifiers.org/hco/4/GRCh38#73450970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90653086-C-A

73451144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90653241-A-G

73451183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90653281-C-T

73451218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90653319-G-T

73452150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654119-T-G

73452152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654121-G-A

73452194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654164-C-G

73452199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654169-T-G

73452259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654236-A-G

73452259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654236-A-T

http://identifiers.org/hco/4/GRCh38#73452261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90654238-C-A

73452261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654238-C-T

http://identifiers.org/hco/4/GRCh38#73452262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90654239-C-A

73452262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654239-C-T

73452303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654280-G-T

73452317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654294-A-T

73452326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654303-G-A

73452351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654329-T-C

73452580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90654559-T-A

73452631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90654610-A-T

http://identifiers.org/hco/4/GRCh38#73452718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90654665-C-A

http://identifiers.org/hco/4/GRCh38#73452741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90654688-C-A

73452820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654769-G-A

73452928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654873-T-C

73452964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654904-A-G

73453086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90654999-T-C

73453226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655145-T-C

73453344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655253-G-A

http://identifiers.org/hco/4/GRCh38#73453431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655334-C-A

73453431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655334-C-G

73453488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655389-G-T

73453538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90655443-A-G

http://identifiers.org/hco/4/GRCh38#73453582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655483-A-C

73453582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90655483-A-G

73453582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90655483-A-T

http://identifiers.org/hco/4/GRCh38#73453583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655484-C-A

73453583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90655484-C-G

73453583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90655484-C-T

http://identifiers.org/hco/4/GRCh38#73453629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655528-A-C

73453647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655546-T-A

73453647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655546-T-C

73453698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655585-G-T

http://identifiers.org/hco/4/GRCh38#73453703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655590-C-A

73453714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655601-T-C

73453714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655601-T-G

73453716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655609-G-A

http://identifiers.org/hco/4/GRCh38#73453761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655653-A-C

73453822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90655714-T-C

73453901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655793-C-T

http://identifiers.org/hco/4/GRCh38#73453922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90655813-A-C

73453922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655813-A-G

73453930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655821-T-C

73453930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655821-T-G

73453966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655857-G-T

73454028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90655907-A-G

73454175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90656040-G-A

73454208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90656073-G-A

73454208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90656073-G-T

73455190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90656239-T-C

73455232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90656285-T-G

73455373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656418-G-C

73455373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656418-G-T

http://identifiers.org/hco/4/GRCh38#73455408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90656458-A-C

73455408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656458-A-G

73455408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656458-A-T

73455421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656471-T-A

73455421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90656471-T-G

http://identifiers.org/hco/4/GRCh38#73455677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90656626-C-A

http://identifiers.org/hco/4/GRCh38#73455722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90656660-A-C

http://identifiers.org/hco/4/GRCh38#73455729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#90656667-C-A

73455729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90656667-C-G

73455729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 317
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90656667-C-T