56648136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77234974-C-T

56648205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235040-T-C

56648230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235108-T-A

56648275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235151-T-C

56648311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235186-A-G

56648321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235196-G-C

56648382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235254-T-C

56648419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235291-T-A

56648491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235358-T-C

56648562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235434-G-A

56648562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235434-G-T

56648658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235528-A-G

56648658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235528-A-T

56648666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235536-G-T

56648676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235547-G-C

56648689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 77235560-T-C

56648836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235702-A-G

56648873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235739-G-T

56648932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235794-C-G

56648932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235794-C-T

56648974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235836-G-A

56648974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235836-G-T

http://identifiers.org/hco/4/GRCh38#56649009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77235846-C-A

56649009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235846-C-T

56649042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235877-C-T

http://identifiers.org/hco/4/GRCh38#56649124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77235925-C-A

56649124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235925-C-T

56649183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235981-T-C

56649209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77235992-C-T

56649263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236048-T-C

56649263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236048-T-G

56649287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236071-G-T

56649324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236100-A-T

56649345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236121-C-T

56649411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236178-A-G

56649436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236204-G-A

56649436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236204-G-C

56649499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236268-G-T

http://identifiers.org/hco/4/GRCh38#56649585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236328-C-A

56649592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236335-T-C

56649755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236495-C-T

56649760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236500-A-T

56649777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236517-G-A

http://identifiers.org/hco/4/GRCh38#56649884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236580-C-A

56649961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236631-A-G

http://identifiers.org/hco/4/GRCh38#56650046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236708-A-C

56650046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236708-A-G

http://identifiers.org/hco/4/GRCh38#56650074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236738-C-A

56650074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236738-C-T

http://identifiers.org/hco/4/GRCh38#56650114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236764-C-A

56650114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236764-C-T

http://identifiers.org/hco/4/GRCh38#56650123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236773-C-A

http://identifiers.org/hco/4/GRCh38#56650183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77236828-C-A

56650183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236828-C-G

56650218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236866-G-A

56650300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77236951-G-T

56650333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237005-G-A

56650333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237005-G-T

56650393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237078-G-A

56650393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237078-G-T

http://identifiers.org/hco/4/GRCh38#56650417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77237088-C-A

56650417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237088-C-T

56650421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237105-A-G

56650431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237115-G-C

56650438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237122-G-T

56650559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237240-G-A

56650559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237240-G-T

http://identifiers.org/hco/4/GRCh38#56650569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77237250-C-A

56650569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237250-C-T

56650588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237268-G-A

56650588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237268-G-C

56650588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237268-G-T

http://identifiers.org/hco/4/GRCh38#56650633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77237318-C-A

56650633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237318-C-T

http://identifiers.org/hco/4/GRCh38#56650727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77237409-C-A

56650727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77237409-C-T

56650733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77237415-A-G

56650790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77237470-C-T

56650837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237799-T-C

56650868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237825-G-T

56650938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237879-G-A

56650938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237879-G-T

56650977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237916-T-G

http://identifiers.org/hco/4/GRCh38#56650995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77237934-C-A

56650995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237934-C-T

56651012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237951-G-A

56651012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77237951-G-T

56651086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77238029-T-C

http://identifiers.org/hco/4/GRCh38#56651211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77238143-C-A

56651293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238228-G-A

56651293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238228-G-T

56651307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238243-C-T

56651328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238264-T-A

56651345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238304-A-G

56651525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238503-G-T

56651611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238589-G-A

56651649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238627-G-C

56651880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238820-G-T

56651905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77238845-T-C

56652060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77239425-T-C

http://identifiers.org/hco/4/GRCh38#56652075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77239440-A-C

56652153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77239497-T-C

56652224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77239636-C-T

56653410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77240290-G-A

56653631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77240468-G-A

56653893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77240670-C-T

56654047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77240818-T-C

56654057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77240828-G-A

http://identifiers.org/hco/4/GRCh38#56654104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77240880-C-A

56654272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77241008-G-A

56654310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77241110-T-C

56654920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77241872-A-G

56654932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77241885-A-G

56655000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77241959-G-C

56655189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron variant
orthologous variants: 77242130-A-G

56655388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77242373-G-T

56655483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77242459-G-A

56655582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77242559-A-G

56655640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242595-G-C

56655673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242609-G-C

56655878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77242734-G-T

56655893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77242749-G-C

http://identifiers.org/hco/4/GRCh38#56655968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77242824-C-A

56655968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77242824-C-G

56655968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77242824-C-T

56656092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242906-C-G

56656092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242906-C-T

56656122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242916-C-T

http://identifiers.org/hco/4/GRCh38#56656237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77242955-C-A

56656237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242955-C-T

56656258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242970-T-A

56656258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242970-T-C

56656258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77242970-T-G

56656510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77243169-G-A

56656510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77243169-G-C

56656510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77243169-G-T

56656555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243213-G-A

56656555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243213-G-T

http://identifiers.org/hco/4/GRCh38#56656569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77243227-C-A

56656569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243227-C-T

http://identifiers.org/hco/4/GRCh38#56656629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77243271-C-A

56656629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243271-C-T

56656630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243272-G-A

56656665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243334-A-G

56657160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243824-T-C

56657501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244100-C-T

56657637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244229-A-G

56657656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244248-G-T

56657677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244305-G-T

http://identifiers.org/hco/4/GRCh38#56657685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77244314-C-A

56657685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244314-C-G

56657685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244314-C-T

56657689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244318-G-A

56657689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244318-G-T

56657780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77244564-C-G

56657855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77244700-C-G

56657857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77244702-G-C

56657869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77244714-A-G

http://identifiers.org/hco/4/GRCh38#56657870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77244715-C-A

56657891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77244736-G-C

56657966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244804-G-A

56657966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244804-G-T

56657969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244807-T-C

56658014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244848-G-A

56658014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244848-G-C

56658066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77244897-C-T

http://identifiers.org/hco/4/GRCh38#56659022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77245847-C-A

56659102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245897-G-T

56659344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246370-G-T

56659366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246394-A-G

http://identifiers.org/hco/4/GRCh38#56659683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77247207-C-A

56661949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247977-G-A

56661949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247977-G-C

http://identifiers.org/hco/4/GRCh38#56662300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77248244-A-C

56662352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248296-C-T

http://identifiers.org/hco/4/GRCh38#56662502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

56662502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-T

56662979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248593-G-A

http://identifiers.org/hco/4/GRCh38#56663037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77248650-C-A

http://identifiers.org/hco/4/GRCh38#56663185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
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#77248786-A-C

56663232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248832-G-A

56663232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248832-G-T

56663250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248851-G-A

56663250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248851-G-C

56663250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248851-G-T

56663306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77248905-T-C

56663443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77249048-G-A

56663443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77249048-G-T

http://identifiers.org/hco/4/GRCh38#56663784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -C-A

56663809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77249100-T-A

56663809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77249100-T-C

http://identifiers.org/hco/4/GRCh38#56663849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77249140-C-A

http://identifiers.org/hco/4/GRCh38#56664462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77249830-C-A

56664466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77249834-G-A

http://identifiers.org/hco/4/GRCh38#56664667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77250042-C-A

56664667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250042-C-T

56664786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250161-C-G

56664786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250161-C-T

http://identifiers.org/hco/4/GRCh38#56664796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77250171-C-A

56664796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250171-C-T

56664841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250214-G-T

56664858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250229-T-A

http://identifiers.org/hco/4/GRCh38#56665823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77250392-C-A

56666047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250581-A-G

56666247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250730-A-G

56666253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250736-A-G

56666292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250779-T-G

56666465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77250928-G-C

56666563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77251033-A-T

56666858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77251276-C-G

56666910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77251325-A-G

56667105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77251520-C-T

56668422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252807-G-T

56668752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252992-A-T

56668753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252993-A-G

56668980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253212-G-A

56669130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253349-G-C

56669169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253393-A-G

http://identifiers.org/hco/4/GRCh38#56669245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77253464-A-C

56669280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253499-G-A

56669377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253593-C-T

56669477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253621-G-A

56670160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254008-A-G

56670194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254042-C-T

56670229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254073-C-T

56670555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254419-T-C

56670555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254419-T-G

http://identifiers.org/hco/4/GRCh38#56670887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77254543-C-A

56671254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254866-G-A

56671363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255008-T-A

56671399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255044-A-G

56671426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255071-A-G

56671735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255376-G-C

56671750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255387-A-G

56672079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255690-A-G

56672151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255715-G-A

56672203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255764-G-A

56673585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257108-T-C

56673626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257136-T-C

56673708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257220-T-A

http://identifiers.org/hco/4/GRCh38#56674137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77257539-C-A

56674376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257740-A-G

56674417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257783-C-T

56674485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257851-T-C

56674587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257941-G-A

56674587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257941-G-T

56676432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259291-A-T

56676442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259301-G-T

56676638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259476-C-T

http://identifiers.org/hco/4/GRCh38#56676641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77259479-C-A

56676641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259479-C-T

56676674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259512-G-T

http://identifiers.org/hco/4/GRCh38#56676715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77259542-C-A

56677771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260331-C-G

http://identifiers.org/hco/4/GRCh38#56680007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77260675-C-A

56680111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260785-A-G

56680112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260786-G-A

http://identifiers.org/hco/4/GRCh38#56680119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77260793-C-A

56680119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260793-C-T

56680144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260846-G-A

56680144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260846-G-T

56680208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77260916-G-T

56680293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261798-A-G

56680305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261810-A-G

http://identifiers.org/hco/4/GRCh38#56680327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77261831-C-A

http://identifiers.org/hco/4/GRCh38#56680371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77261869-C-A

56680383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261881-G-A

56680383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261881-G-T

56680393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261893-T-C

56680532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77261979-T-C

56680619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262060-C-T

http://identifiers.org/hco/4/GRCh38#56680653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77262100-C-A

56680675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262122-G-A

56680682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262129-G-A

56680682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262129-G-T

56680775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262215-A-G

56680801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262244-G-C

56681025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77262438-T-C

56681042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 77262451-G-A

56681042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 77262451-G-T

56681114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77262544-G-A

56681300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262730-G-T

56681317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262747-T-C

56681344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262772-A-G

56681344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262772-A-T

http://identifiers.org/hco/4/GRCh38#56681445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77262873-C-A

56681445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262873-C-G

56681445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262873-C-T

56681523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262947-A-G

56681586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77262987-A-G

56681601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77263002-A-T

56681666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 77263057-C-T

56681725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263115-G-A

56681725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263115-G-C

56681725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263115-G-T

http://identifiers.org/hco/4/GRCh38#56681730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77263120-C-A

56681730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263120-C-T

56681733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263123-G-A

56681733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24961
most severe consequence: 5 prime UTR variant
orthologous variants: 77263123-G-T