24420980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56897208-T-C

http://identifiers.org/hco/13/GRCh38#24420982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56897206-C-A

24420982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56897206-C-T

24421006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56897179-T-C

24421025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56897163-A-G

24421278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56896729-T-G

24421306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56896701-G-A

24421306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56896701-G-T

24426343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56893284-A-G

24433916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56887332-A-G

24434180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886577-G-T

24434264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886530-T-A

24434264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886530-T-C

24434264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56886530-T-G

24441750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56877071-T-C

http://identifiers.org/hco/13/GRCh38#24441814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875450-C-A

24441850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56875421-T-C

24441926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56875345-C-T

24441964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56875307-T-C

24442058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875221-G-A

24442058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875221-G-T

24442065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875214-G-A

24442065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875214-G-C

24442065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875214-G-T

24442072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875207-T-A

24442072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875207-T-C

24442072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875207-T-G

http://identifiers.org/hco/13/GRCh38#24442099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56875182-C-A

24442099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875182-C-G

24442099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56875182-C-T

24442565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873306-A-G

24442583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56873288-T-A

24442583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56873288-T-C

http://identifiers.org/hco/13/GRCh38#24442696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56873171-A-C

24442696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56873171-A-G

24442873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872544-A-G

http://identifiers.org/hco/13/GRCh38#24442937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56872447-C-A

http://identifiers.org/hco/13/GRCh38#24443027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56872322-C-A

24443085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872273-G-A

24443129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872227-T-A

http://identifiers.org/hco/13/GRCh38#24443182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56872189-A-C

24443230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872144-C-T

24443250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872124-G-T

24443362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56872022-C-T

24443458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871927-T-C

24443502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871884-G-A

24443502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871884-G-T

http://identifiers.org/hco/13/GRCh38#24443512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56871874-C-A

24443518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871868-T-A

24443518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871868-T-C

24443548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871844-C-T

24443591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871803-A-G

24443651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56871746-T-C

24443666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56871731-T-C

24443702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56871695-A-G

24443707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56871690-T-G

24443778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871619-A-G

24443778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56871619-A-T

24446784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866900-T-A

24446784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866900-T-G

24446817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866866-G-T

http://identifiers.org/hco/13/GRCh38#24446910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866794-C-A

http://identifiers.org/hco/13/GRCh38#24446927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866776-C-A

24446927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866776-C-T

24446934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866769-G-T

24446950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866753-G-A

24447080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56866635-T-C

24447098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56866617-G-A

24447184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56866531-T-C

http://identifiers.org/hco/13/GRCh38#24447187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866528-C-A

24447187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 56866528-C-G

24447219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866497-A-G

24447231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866458-G-A

24447231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866458-G-T

24447238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866408-G-C

24447238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866408-G-T

http://identifiers.org/hco/13/GRCh38#24447265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56866338-C-A

24447265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866338-C-G

24447265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866338-C-T

24447304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866308-T-A

24447304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866308-T-C

24447304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56866308-T-G

24449649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56865023-A-G

24449706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864964-T-C

24449770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56864892-G-A

24449770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56864892-G-T

24449832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864830-C-G

24449832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864830-C-T

http://identifiers.org/hco/13/GRCh38#24449851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56864027-C-A

24449851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864027-C-T

24451470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862397-C-T

24451637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862237-T-C

24451838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862084-A-G

24451885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862059-G-T

24451917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862026-A-G

24451942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861995-G-A

24451942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861995-G-T

http://identifiers.org/hco/13/GRCh38#24451957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56861987-C-A

24451957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861987-C-T

24451994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861945-G-A

24451994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861945-G-C

24451994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861945-G-T

24452042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861898-A-G

http://identifiers.org/hco/13/GRCh38#24452045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56861895-C-A

24452045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861895-C-G

24452045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861895-C-T

24452055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861885-A-G

24452143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861875-T-C

24452144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861874-A-G

24452187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861850-A-G

24452202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861842-C-T

24452240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861827-G-T

24452245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861822-G-A

24452245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861822-G-T

24452290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861777-T-C

24452290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861777-T-G

24452381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861688-A-G

24452394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56861671-T-A

24453574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859715-C-T

24453604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56859689-C-T

24453605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56859688-C-T

24454452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858679-T-G

http://identifiers.org/hco/13/GRCh38#24454877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56858224-C-A

http://identifiers.org/hco/13/GRCh38#24454913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56858191-C-A

24454913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858191-C-G

24454913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858191-C-T

24454954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858149-T-A

24454954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858149-T-C

24454961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858142-A-G

24454962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858141-A-G

http://identifiers.org/hco/13/GRCh38#24455125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56857996-A-C

24455125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56857996-A-G

24455148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56857973-T-C

24455158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56857963-T-C

24455159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56857962-G-C

24455165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56857956-G-A

24455165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56857956-G-C

24455165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56857956-G-T

24455234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857888-T-A

24455249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857873-T-C

24455310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857492-A-G

24455310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857492-A-T

http://identifiers.org/hco/13/GRCh38#24455311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56857491-A-C

24455317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857485-T-A

24455317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857485-T-C

24455329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857473-G-A

24455329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857473-G-T

24455496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856716-T-C

24455496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856716-T-G

24455497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856715-A-G

24455508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856704-A-G

24455508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856704-A-T

24455523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856689-G-A

24455573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856655-C-T

24456316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853949-T-C

24456384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56853881-A-G

24456399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56853866-A-G

http://identifiers.org/hco/13/GRCh38#24456501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56853763-A-C

24456543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853721-T-C

24456549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853715-G-T

24456603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853661-T-A

24456603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853661-T-C

24457092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853538-T-C

24457142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853489-T-C

http://identifiers.org/hco/13/GRCh38#24457192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56853439-A-C

24457430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853222-G-C

24457451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56853212-C-T

http://identifiers.org/hco/13/GRCh38#24458957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56852306-C-A

24458957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852306-C-T

24459011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56852254-T-A

24459117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56852147-G-A

24459117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56852147-G-T

24459201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851972-G-A

24459201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851972-G-T

24459256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56851909-G-A

24459332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851833-T-A

24459332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851833-T-C

24459332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851833-T-G

24459383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851791-T-C

24459393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851781-G-A

24459393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851781-G-T

24459414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851757-G-A

24459414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851757-G-T

24459418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851753-G-A

24459418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56851753-G-T

http://identifiers.org/hco/13/GRCh38#24459456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56851715-A-C

24459496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851657-G-T

24459520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851631-T-C

24459594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851588-G-T

24459595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851587-T-A

24459595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851587-T-C

24459595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851587-T-G

24459945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851316-G-A

24460032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56851213-A-G

24460079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56851166-T-A

24460152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56851093-A-G

24460289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850983-C-T

24460375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56850904-C-T

24468912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-A

24468912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-C

24468912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848393-G-T

24468936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848369-A-T

24468947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848358-T-A

24468947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848358-T-C

http://identifiers.org/hco/13/GRCh38#24468991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848329-C-A

24468991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848329-C-T

24468994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848326-T-C

24468995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848325-A-G

24468995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848325-A-T

24469025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56848294-G-A

24469025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56848294-G-T

24469079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56848240-T-C

http://identifiers.org/hco/13/GRCh38#24469108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56848211-A-C

24469108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 56848211-A-G

24469108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 56848211-A-T

24469122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848037-G-A

24469122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848037-G-T

24469135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848024-T-C

24469155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848004-T-C

24469181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847978-T-C

24469193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847966-A-G

http://identifiers.org/hco/13/GRCh38#24469195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56847964-A-C

24469239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847921-T-A

24469239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847921-T-C

24469239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847921-T-G

24469248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847912-G-A

24469248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847912-G-C

24469248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847912-G-T

24469272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847889-G-A

24469428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847731-T-C

24469535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56847652-C-G

24469841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845990-T-C

24469859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845976-G-A

http://identifiers.org/hco/13/GRCh38#24469860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56845975-C-A

24469860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845975-C-T

24469874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845965-G-A

24469922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56845919-A-T

24469940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56845901-A-G

24470040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845795-A-G

24470040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845795-A-T

24470060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845773-A-G

http://identifiers.org/hco/13/GRCh38#24470091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56845747-C-A

24470091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845747-C-T

24475437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56845037-G-A

24475714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844760-T-A

24475714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844760-T-C

24475714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844760-T-G

http://identifiers.org/hco/13/GRCh38#24477701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56840362-C-A

24477701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56840362-C-T

http://identifiers.org/hco/13/GRCh38#24477707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56840356-C-A

24477707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56840356-C-T

24477853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56840210-T-C

24478196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56839799-C-G

24478235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56839760-G-C

24478252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56839743-C-G

24478252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56839743-C-T

http://identifiers.org/hco/13/GRCh38#24478298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56839697-C-A

24478298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839697-C-T

24478355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839312-G-A

24478355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839312-G-C

24478355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839312-G-T

24484620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835913-A-G

24486097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835234-G-T

24486103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835228-A-G

http://identifiers.org/hco/13/GRCh38#24486120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56835214-A-C

24486194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56835142-T-C

24486207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56835129-T-C

24490604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832925-C-T

24490622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832908-G-A

24490622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832908-G-T

24490716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56832821-G-C

24490846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832692-A-G

24492513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56830760-T-C

24492821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830460-C-G

24492821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830460-C-T

24492876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830407-G-C

24492984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830315-C-T

http://identifiers.org/hco/13/GRCh38#24492996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56830303-A-C

24493052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830248-A-T

24493087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830213-T-C

24493218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830156-G-A

24493472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830006-A-G

http://identifiers.org/hco/13/GRCh38#24493524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56829954-C-A

24493524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829954-C-T

24493903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829234-T-C

24493938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829192-C-T

24493963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829164-T-C

24493974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829153-G-C

24494264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828857-T-C

24494280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56828847-C-T

http://identifiers.org/hco/13/GRCh38#24494571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56827970-A-C

24494715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56827826-C-G

24494752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827789-A-G

24494771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827768-A-G

24494771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827768-A-T

http://identifiers.org/hco/13/GRCh38#24494784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56827755-A-C

24494784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827755-A-G

24498180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56827374-G-A

24498180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56827374-G-C

http://identifiers.org/hco/13/GRCh38#24498225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56827338-C-A

24498225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56827338-C-G

24498239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827324-A-G

24498290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827277-T-C

24498298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827269-T-C

24498321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827242-G-A

24498321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827242-G-T

24498353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826988-A-G

24498380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826961-T-A

24498380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826961-T-C

24499131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826118-A-G

24499173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826061-A-G

24499229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56826006-G-A

24499248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-T-A

24499248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-T-C

24499248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825987-T-G

24499249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825986-T-A

24499249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825986-T-C

24499281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825969-A-G

24499281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825969-A-T

http://identifiers.org/hco/13/GRCh38#24499287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56825963-A-C

24499287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825963-A-G

24499287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825963-A-T

http://identifiers.org/hco/13/GRCh38#24499307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56825943-C-A

24499307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56825943-C-T

24499345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56825905-G-A

24499345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56825905-G-C

24499347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56825903-T-C

24499396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825859-A-T

24500266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825280-A-G

24500384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 56825202-T-C

24501396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823420-G-C

24501396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56823420-G-T

24501661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56823182-T-C

24501674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56823169-A-G

24501695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56823151-T-C

24501770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56823076-T-G

24501848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822998-G-A

24503282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56822099-T-C

http://identifiers.org/hco/13/GRCh38#24503315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56822069-A-C

24503500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821879-G-A

24503500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821879-G-C

24503500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821879-G-T

24503556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821833-G-A

24503556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821833-G-T

http://identifiers.org/hco/13/GRCh38#24503557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#56821832-C-A

24503557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821832-C-T

24503559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821830-A-G

24503559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56821830-A-T