35490111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43382145-G-A

35490111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43382145-G-T

35490166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43382193-A-G

35490177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43382204-G-A

35490177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43382204-G-C

35490177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43382204-G-T

35490199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43382226-A-G

http://identifiers.org/hco/9/GRCh38#35490297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43382313-C-A

35490297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43382313-C-T

35490350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43382355-G-T

http://identifiers.org/hco/9/GRCh38#35490489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43382481-C-A

35490650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43382613-C-T

http://identifiers.org/hco/9/GRCh38#35490660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43382623-C-A

35490823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43382776-C-T

35492060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43383931-A-G

35492071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43383945-G-A

35492459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384338-G-A

35492459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384338-G-T

http://identifiers.org/hco/9/GRCh38#35492463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43384342-C-A

35492466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384345-A-G

35492545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384415-G-C

35492608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384484-G-C

35492668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384551-T-C

35492839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384892-C-T

35492847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43384900-C-T

35501743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43387172-C-T

35501928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43387338-A-T

35502034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43387433-G-C

35502059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43387456-C-T

35509305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43391636-C-T

35509632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43391953-A-G

35510798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394315-G-T

35510815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394333-C-G

35511100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394596-C-T

35511144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394643-A-G

35511229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43394742-A-G

35511268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43394776-G-T

35511484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43394916-C-G

35511505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43394938-C-G

35511856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395232-T-C

35514474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395608-G-A

35514479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395613-A-G

35514539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395660-G-C

35514613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395766-G-T

35514699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395853-A-T

35514764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395900-C-T

35514776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43395912-T-A

35515358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396410-A-T

35515380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396432-G-C

35515526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396532-A-G

35515700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43396649-T-A

35516539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397167-T-C

35516543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397171-A-G

35516925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397739-A-G

35517008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43397818-C-T

35517201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398041-T-C

35517292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398111-G-A

35517441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398223-A-G

35517570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398346-T-A

http://identifiers.org/hco/9/GRCh38#35517799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43398506-C-A

35517799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398506-C-T

35518073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398780-G-A

35518131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398827-A-G

35518185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398887-T-C

35518280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398961-G-A

35518290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43398971-G-T

35518482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399146-G-A

35518551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399186-T-C

35518748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399380-G-C

35518854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399486-A-T

35518879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399506-G-A

35518904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399530-T-C

35518939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399565-G-A

35519000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399634-T-C

35519020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399654-G-A

35519030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399664-T-A

35519142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399770-G-A

35519313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43399942-C-G

http://identifiers.org/hco/9/GRCh38#35519361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43399989-A-C

35519361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43399989-A-G

35519451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43400064-G-A

http://identifiers.org/hco/9/GRCh38#35519453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43400066-A-C

35519466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43400077-G-A

35519602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400186-A-G

35519604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400188-G-A

35519604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400188-G-T

35519904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400600-G-T

35519936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400634-G-A

http://identifiers.org/hco/9/GRCh38#35520043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43400706-A-C

35520049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400712-C-G

35520067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400728-T-C

http://identifiers.org/hco/9/GRCh38#35520084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43400745-A-C

35520286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400917-G-C

35520353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43400978-G-C

35520432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401079-C-G

35520678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401291-C-T

35521302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401851-G-C

35521437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401974-C-G

35521443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401980-T-A

35521453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43401987-G-A

35521578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402227-C-G

35521668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402287-G-T

35521807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402412-T-C

35521807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402412-T-G

35521948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402549-T-C

35522132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402705-C-T

35522197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43402740-G-A

35522323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403317-T-A

35522398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403428-G-A

35522589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43403629-C-T

35522695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404125-G-C

35537269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404658-G-C

35537462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404838-T-G

35537592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43404937-G-A

35537696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43405018-T-C

35538004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43405622-C-T

35538286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43405880-G-T

35538356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43405950-G-A

35538495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406126-C-G

35538498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406129-G-A

35538522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406154-A-G

http://identifiers.org/hco/9/GRCh38#35538531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406163-C-A

35538531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406163-C-G

35538540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406178-C-T

35538553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406191-G-T

35538636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406280-T-C

35538646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406285-G-T

35538664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43406303-A-G

35538691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406332-C-T

35538692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406333-T-C

http://identifiers.org/hco/9/GRCh38#35538713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406353-C-A

35538888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406521-A-G

35538894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406533-G-A

35538894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406533-G-T

http://identifiers.org/hco/9/GRCh38#35538983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406621-A-C

35538983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406621-A-G

35539031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406670-G-A

35539031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406670-G-T

35539049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406688-T-C

35539052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406691-G-C

35539052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406691-G-T

35539061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406700-C-T

http://identifiers.org/hco/9/GRCh38#35539097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406735-C-A

35539102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406740-G-A

35539102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43406740-G-T

35539140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406775-G-A

35539140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43406775-G-T

http://identifiers.org/hco/9/GRCh38#35539249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406862-A-C

http://identifiers.org/hco/9/GRCh38#35539254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43406867-C-A

35539254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406867-C-T

35539303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406894-G-A

35539373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43406975-C-T

http://identifiers.org/hco/9/GRCh38#35539466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43407110-C-A

35539547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407190-C-G

http://identifiers.org/hco/9/GRCh38#35539799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43407407-A-C

35539862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407453-T-C

35539881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407471-C-T

35539944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407533-C-T

35540664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407924-T-C

35540664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407924-T-G

35540667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407927-G-A

35540667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407927-G-T

35540735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407980-G-A

35540751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43407996-A-G

35540789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408027-G-A

35540853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408084-A-G

35540863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408094-T-C

http://identifiers.org/hco/9/GRCh38#35540909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43408135-C-A

35541143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408413-G-A

35541535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408733-C-T

35541577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408762-G-C

35541584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43408769-T-C

http://identifiers.org/hco/9/GRCh38#35545060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43412678-C-A

http://identifiers.org/hco/9/GRCh38#35545145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43412761-C-A

35545204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43412819-G-A

35545316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43412908-T-C

35545931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43413993-A-G

http://identifiers.org/hco/9/GRCh38#35546229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414435-A-C

35546241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414447-G-T

35546293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414498-G-A

35546293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414498-G-T

http://identifiers.org/hco/9/GRCh38#35546307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414513-C-A

35546307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414513-C-T

http://identifiers.org/hco/9/GRCh38#35546333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414540-C-A

35546333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414540-C-T

35546399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414606-T-C

35546399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43414606-T-G

35546455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43414653-G-A

35546455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43414653-G-T

35546551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414749-G-A

35546551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43414749-G-T

http://identifiers.org/hco/9/GRCh38#35546584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414782-C-A

35546584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414782-C-T

35546629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414827-T-C

35546629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414827-T-G

http://identifiers.org/hco/9/GRCh38#35546659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414857-C-A

35546659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414857-C-T

35546665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414863-T-A

35546665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414863-T-C

35546668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43414866-G-T

http://identifiers.org/hco/9/GRCh38#35546736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414934-C-A

http://identifiers.org/hco/9/GRCh38#35546756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414954-C-A

35546756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43414954-C-T

http://identifiers.org/hco/9/GRCh38#35546770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43414968-C-A

35546770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43414968-C-T

35546821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43415019-C-T

35546864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415062-G-A

35546875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43415073-T-C

35546994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415189-C-T

http://identifiers.org/hco/9/GRCh38#35547007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43415202-A-C

35547009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415204-G-A

35547016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43415211-G-A

http://identifiers.org/hco/9/GRCh38#35547080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43415272-A-C

35547170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415362-G-A

35547352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43415544-A-G

http://identifiers.org/hco/9/GRCh38#35547466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43415658-A-C

35547466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43415658-A-G

35547548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415740-G-A

35547621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43415813-G-A

35547914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43416106-A-G

35547973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43416165-T-C

35548024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43416216-C-T

http://identifiers.org/hco/9/GRCh38#35548090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43416282-C-A

35548125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43416317-G-A

35548125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43416317-G-T

35548153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43416345-T-C

35548354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43416546-A-G

http://identifiers.org/hco/9/GRCh38#35548497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43416680-A-C

35548515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43416698-A-G

35548517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43416700-G-A

35548517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43416700-G-C

35548517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43416700-G-T

35548675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416792-C-T

http://identifiers.org/hco/9/GRCh38#35548710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43416808-A-C

35548710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416808-A-G

35548717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416815-A-G

35548854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416889-A-G

http://identifiers.org/hco/9/GRCh38#35548931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43416955-C-A

35548999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43416999-T-C

35549091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417045-A-G

http://identifiers.org/hco/9/GRCh38#35549275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43417123-A-C

35549318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417148-G-A

35549318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417148-G-T

http://identifiers.org/hco/9/GRCh38#35550598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43417810-C-A

35550598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417810-C-G

35550598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417810-C-T

35550599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417811-T-A

35550599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417811-T-C

35550599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417811-T-G

35550607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417819-C-T

35550631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417844-T-A

35550643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43417856-G-C

35552409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419316-C-T

35552635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419525-T-C

35552636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419526-A-G

35552651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419538-C-T

35553269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419693-G-A

35553331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419748-T-G

35553472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419871-A-T

35553493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419883-G-A

35553496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419886-A-G

35553560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43419935-G-A

35553875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420153-A-G

http://identifiers.org/hco/9/GRCh38#35553900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#43420178-C-A

35554296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420703-C-G

35554314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43420719-G-A

35554580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421130-C-T

http://identifiers.org/hco/9/GRCh38#35554611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43421166-A-C

35554633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421195-G-A

35554644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421202-A-G

35554805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421354-C-T

35554881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421415-C-G

35554921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421451-T-C

http://identifiers.org/hco/9/GRCh38#35554962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43421499-C-A

35555042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421586-T-A

35555048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43421592-C-T

35555075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43421620-G-T

http://identifiers.org/hco/9/GRCh38#35555118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43421663-A-C

http://identifiers.org/hco/9/GRCh38#35555136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43421681-C-A

35555136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421681-C-T

35555216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43421764-G-A

35555216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43421764-G-C

35555226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421774-T-C

35555260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43421808-G-T

35555304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421852-C-T

35555334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421882-G-A

http://identifiers.org/hco/9/GRCh38#35555406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43421954-C-A

35555406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421954-C-T

35555424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43421972-T-C

35555454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43422002-T-C

35555470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43422018-A-G

35555485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43422033-C-G

35555587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43422135-C-T

http://identifiers.org/hco/9/GRCh38#35555641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422189-C-A

35555641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 43422189-C-T

http://identifiers.org/hco/9/GRCh38#35555705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422253-C-A

35555705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422253-C-T

http://identifiers.org/hco/9/GRCh38#35555791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422310-C-A

35555791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422310-C-G

http://identifiers.org/hco/9/GRCh38#35555825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422323-C-A

35555825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422323-C-G

35555825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422323-C-T

35555828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422326-A-G

35555828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422326-A-T

http://identifiers.org/hco/9/GRCh38#35555830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422328-C-A

35555830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422328-C-T

35555876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422377-C-G

http://identifiers.org/hco/9/GRCh38#35556147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43422636-C-A

35556168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422659-G-A

35556168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422659-G-T

35556270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422681-T-C

35556281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422692-C-T

35556321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43422732-G-A

35556324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43422735-G-A

35556411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43422822-C-T

35556463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43422875-C-G

35557851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423611-A-G

35557882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423642-A-G

35557885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423646-G-A

35557885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423646-G-T

35557980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43423741-C-G

35557984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43423745-G-A

35557984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43423745-G-C

35558050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423799-A-G

http://identifiers.org/hco/9/GRCh38#35558098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43423831-A-C

35558098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423831-A-T

35558126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423859-T-C

35558153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423875-T-G

35558156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43423878-G-A

http://identifiers.org/hco/9/GRCh38#35558159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43423881-C-A

35558280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43424003-G-A

35558559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43424281-C-T

35558560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43424282-C-G

http://identifiers.org/hco/9/GRCh38#35558582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424302-C-A

35558582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424302-C-G

35558609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424326-T-G

http://identifiers.org/hco/9/GRCh38#35558626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424334-C-A

35558628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424336-C-T

http://identifiers.org/hco/9/GRCh38#35558685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424398-C-A

35558794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424487-A-G

35558887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424578-A-G

35558895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424586-C-T

35558943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424632-C-T

35559015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424695-C-G

35559084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424761-T-C

35559113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424789-G-A

35559113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424789-G-C

35559113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424789-G-T

35559147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424820-G-A

35559147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424820-G-T

http://identifiers.org/hco/9/GRCh38#35559156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424829-C-A

35559156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424829-C-G

35559156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424829-C-T

http://identifiers.org/hco/9/GRCh38#35559190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424864-C-A

35559190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424864-C-T

35559215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424887-T-C

http://identifiers.org/hco/9/GRCh38#35559230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424902-C-A

35559230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43424902-C-G

35559230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43424902-C-T

35559287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424959-C-T

35559295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424963-T-C

http://identifiers.org/hco/9/GRCh38#35559296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424964-C-A

35559345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424972-G-A

35559345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424972-G-C

35559345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424972-G-T

http://identifiers.org/hco/9/GRCh38#35559353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424980-A-C

35559353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43424980-A-G

http://identifiers.org/hco/9/GRCh38#35559357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43424984-C-A

35559384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425009-G-T

35559397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425022-G-A

35559397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425022-G-T

http://identifiers.org/hco/9/GRCh38#35559401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425026-C-A

35559401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425026-C-G

35559870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425150-A-G

http://identifiers.org/hco/9/GRCh38#35559896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425175-A-C

35559896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425175-A-G

35559896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425175-A-T

http://identifiers.org/hco/9/GRCh38#35559936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425208-C-A

35559936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43425208-C-T

http://identifiers.org/hco/9/GRCh38#35559964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425234-C-A

http://identifiers.org/hco/9/GRCh38#35560147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425415-C-A

35560147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425415-C-T

35560240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425508-G-C

35560240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425508-G-T

35560402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425664-C-G

35560402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425664-C-T

35560411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425673-A-G

35560492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425754-C-T

35560495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43425757-C-T

http://identifiers.org/hco/9/GRCh38#35560558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43425829-A-C

35560726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426003-G-A

http://identifiers.org/hco/9/GRCh38#35560743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426020-C-A

35560743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426020-C-T

http://identifiers.org/hco/9/GRCh38#35560749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426026-C-A

35560749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426026-C-T

35560759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426036-G-A

35560759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426036-G-T

35560765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426042-G-A

35560765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426042-G-C

http://identifiers.org/hco/9/GRCh38#35560768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426045-C-A

35560768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426045-C-T

http://identifiers.org/hco/9/GRCh38#35560838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426115-C-A

35560838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426115-C-G

35560838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426115-C-T

35560884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426167-G-A

35560884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426167-G-T

35560890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426173-A-T

35560969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426237-G-A

35560969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43426237-G-C

http://identifiers.org/hco/9/GRCh38#35561030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426298-C-A

35561030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426298-C-T

35561046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426314-A-G

35561060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426328-G-C

35561159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43426426-C-T

35561248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426515-A-G

35561248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43426515-A-T

http://identifiers.org/hco/9/GRCh38#35561422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426688-C-A

35561422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426688-C-G

35561439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426706-G-A

35561439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426706-G-C

35561439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426706-G-T

http://identifiers.org/hco/9/GRCh38#35561446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426713-C-A

35561446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426713-C-T

http://identifiers.org/hco/9/GRCh38#35561703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426903-C-A

35561710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426909-C-T

35561741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426940-C-T

http://identifiers.org/hco/9/GRCh38#35561796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#43426983-C-A

35561796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43426983-C-T

35561816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23625
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43427000-G-A