http://identifiers.org/hco/11/GRCh38#32602754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104829620-A-C

32602754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3 prime UTR variant
orthologous variants: 104829620-A-G

http://identifiers.org/hco/11/GRCh38#32602926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104829418-C-A

32602926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 104829418-C-G

32602926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 104829418-C-T

32603102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829226-G-A

32603102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829226-G-T

32603156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829179-G-A

32603156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829179-G-T

32603182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829156-G-A

32603182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104829156-G-T

32603531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828728-T-A

32603556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828708-A-G

32603556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828708-A-T

32603564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828700-A-G

32603934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828244-G-A

32603934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828244-G-T

http://identifiers.org/hco/11/GRCh38#32603939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104828239-C-A

32603939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828239-C-T

http://identifiers.org/hco/11/GRCh38#32603957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104828222-C-A

32603957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828222-C-T

32603958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828221-T-C

32603958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828221-T-G

http://identifiers.org/hco/11/GRCh38#32603989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104828191-C-A

32603989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828191-C-T

32603996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828186-G-A

32604002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828180-G-A

32604013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828161-G-T

http://identifiers.org/hco/11/GRCh38#32604039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104828151-C-A

32604039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104828151-C-T

http://identifiers.org/hco/11/GRCh38#32604058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104828132-C-A

32605536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104827120-C-G

32605691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104827005-G-T

32605873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 104826845-T-A

32606283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104826557-T-C

http://identifiers.org/hco/11/GRCh38#32606374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104826470-C-A

32606537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104826233-T-C

32606537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104826233-T-G

32606583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104826132-T-G

32606609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104826106-A-G

http://identifiers.org/hco/11/GRCh38#32606791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104825912-C-A

32606791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104825912-C-T

32611085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824992-G-A

32611085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824992-G-C

32611085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824992-G-T

32611151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104824926-G-T

http://identifiers.org/hco/11/GRCh38#32611231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104824846-C-A

32611502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824614-T-C

32611550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824572-T-A

32611919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104824297-T-C

32612598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104823857-G-A

32612647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104823813-G-T

32612782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104823706-G-A

32613047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104823460-T-C

32613128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104823382-T-C

http://identifiers.org/hco/11/GRCh38#32613408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104822909-C-A

32613408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104822909-C-G

32613408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104822909-C-T

32613412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104822905-G-A

32613547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822770-G-A

32613547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822770-G-C

32613596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822727-C-T

32613615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104822708-G-A

32613674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822652-C-T

32613698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822628-A-T

32613740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822586-C-T

32613817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822509-T-C

32613904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822440-T-C

http://identifiers.org/hco/11/GRCh38#32614146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104822201-C-A

32614217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822133-G-A

32614217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104822133-G-C

32614341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104822027-T-C

32614365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104822003-A-G

32614393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104821975-C-G

32614638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 104821727-A-T

32614663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104821702-A-G

32614702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104821663-A-G

32614900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant
orthologous variants: 104821465-G-T

32615138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104821244-G-A

http://identifiers.org/hco/11/GRCh38#32615207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104821149-C-A

32615207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104821149-C-T

32615236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104821120-G-T

32615659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104820713-T-C

32615769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104820610-T-A

32615769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104820610-T-C

32615769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104820610-T-G

32616050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104820293-G-C

32616115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104820225-T-C

http://identifiers.org/hco/11/GRCh38#32616162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104820190-C-A

32616162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104820190-C-T

32622816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104819387-A-G

32622924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104819283-T-A

32622931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104819276-C-T

32622934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104819273-C-T

32635567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815568-T-C

32635581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815554-C-T

http://identifiers.org/hco/11/GRCh38#32635673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104815474-C-A

32635673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815474-C-T

32635800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104815347-T-A

32635923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815248-T-C

32635955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815226-T-A

32635955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815226-T-G

32640220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814665-G-A

32640265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814622-T-C

http://identifiers.org/hco/11/GRCh38#32640325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104813371-C-A

32640355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813345-T-C

32640407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813294-G-T

32641088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812967-T-C

32641322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812011-G-T

http://identifiers.org/hco/11/GRCh38#32641370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104811966-A-C

32641806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811603-T-A

http://identifiers.org/hco/11/GRCh38#32641820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104811588-C-A

32641831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811577-T-C

32641954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811461-T-C

32642060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104811355-A-G

32642176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811239-T-C

32642653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810779-T-C

32642653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810779-T-G

http://identifiers.org/hco/11/GRCh38#32642857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104810587-C-A

32642877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810577-A-T

32643370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810022-G-A

32645960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809980-G-A

32646028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809901-T-C

32646202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809752-A-G

32646588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809213-G-C

32646647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809160-A-G

32646684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809127-T-C

32646689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809122-A-G

32646767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809021-C-T

32646806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808800-C-T

32646927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808561-T-C

32647119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808385-A-G

32647195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808332-C-T

32648216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104807529-G-C

32648994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806945-C-T

32649308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806637-A-G

32649585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806420-C-T

32653124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 104806002-T-C

32653503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805620-T-G

32653832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804408-G-T

32653915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804322-T-A

32653930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804310-T-A

32653930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804310-T-C

32654054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804186-G-T

32654781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104803701-T-C

32654850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104803632-G-A

32654850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104803632-G-T

32657050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802503-C-T

32657269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802305-G-C

32657446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802142-G-T

32658193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800630-A-G

32658289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800551-G-A

32658322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800520-T-C

32658386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800454-A-T

32658755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800175-A-G

32659482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799454-T-A

32659543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799392-C-T

http://identifiers.org/hco/11/GRCh38#32659919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104798774-A-C

32659990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798704-C-T

32660160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798565-G-A

32660160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798565-G-C

32660215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798506-T-A

32668395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104797340-T-G

http://identifiers.org/hco/11/GRCh38#32668700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104797053-C-A

32668700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104797053-C-T

32668820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796941-G-A

32669150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796611-G-A

http://identifiers.org/hco/11/GRCh38#32669242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104796520-C-A

32669242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796520-C-T

http://identifiers.org/hco/11/GRCh38#32670734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104795710-C-A

32670847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104795413-G-A

32675460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104782401-T-A

32675460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104782401-T-C

32675519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104782332-T-C

32675651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104782205-C-T

http://identifiers.org/hco/11/GRCh38#32675693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104782165-C-A

32675715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104782143-A-T

32675793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104782075-A-T

32675874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104781997-G-A

32675874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104781997-G-T

32681100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104777664-T-C

32681387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104777412-T-C

32681479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104777331-G-T

http://identifiers.org/hco/11/GRCh38#32681536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104777262-C-A

http://identifiers.org/hco/11/GRCh38#32681694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104777110-C-A

32682223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104776697-G-A

32682521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104776394-T-A

32682521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104776394-T-C

32682644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104776283-C-T

32682744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104776165-A-G

32683327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104775994-T-C

32683327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104775994-T-G

32683331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104775990-A-G

http://identifiers.org/hco/11/GRCh38#32683418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104775911-A-C

32683418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104775911-A-G

32683477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104775852-C-T

32683578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104775756-G-C

32683578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104775756-G-T

32683621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775719-T-C

32683621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775719-T-G

32683950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775224-G-A

32684009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775161-G-C

32684199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774975-A-G

http://identifiers.org/hco/11/GRCh38#32684211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104774962-C-A

32684211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774962-C-G

32684506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774712-A-G

32684824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774353-G-A

32684905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774233-C-T

http://identifiers.org/hco/11/GRCh38#32684937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104774187-C-A

32684937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774187-C-T

32685028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774028-C-T

32685083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773974-A-G

32685305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773784-T-A

32685305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773784-T-C

32689416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770801-G-C

32689416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770801-G-T

32689561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770658-T-A

32690045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770455-G-C

32690096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770404-C-G

32690230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770278-A-G

32690237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770271-A-G

32690372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770145-A-G

32692299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104769377-C-T

32693079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104768683-G-A

32693346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104768413-G-C

32693346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104768413-G-T

32693351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104768408-T-C

32693351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104768408-T-G

http://identifiers.org/hco/11/GRCh38#32693410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104768348-A-C

http://identifiers.org/hco/11/GRCh38#32699215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104761424-C-A

32699330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104761313-A-G

32700333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104760509-T-C

32700352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104760489-T-C

32700481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104760158-T-G

32700525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104760115-C-T

32701332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104759532-T-C

32702407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757924-T-C

32702524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757610-T-G

32702815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757376-G-A

32702841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757351-A-G

32702859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757333-C-G

32702860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757332-C-T

32702999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104757175-C-G

32714755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104748644-C-T

32715250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104748221-G-A

32715801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747660-A-G

32715991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747500-A-G

32716025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747466-T-C

32716046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747445-C-T

32716294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747024-C-T

32716310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104747008-C-G

32716693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104746390-C-T

32716961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745945-C-T

32717389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745584-G-A

32717740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745293-A-G

32717918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745215-T-C

32717919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745214-T-C

32717929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745204-G-A

32717990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104745138-T-C

http://identifiers.org/hco/11/GRCh38#32718029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104745103-C-A

32718171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744980-G-A

32718171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744980-G-T

32718187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744964-G-C

32718187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744964-G-T

http://identifiers.org/hco/11/GRCh38#32718236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104744918-C-A

32718236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744918-C-T

http://identifiers.org/hco/11/GRCh38#32718261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104744897-A-C

http://identifiers.org/hco/11/GRCh38#32722298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104744577-A-C

32722298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744577-A-T

32722481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104744406-A-G

32723925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104741218-T-C

32724087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104741060-T-C

32724118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104741045-T-C

32724502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104740683-G-T

32724619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104740595-A-G

32724834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104740481-G-C

32759996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104738143-T-C

32760212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104737938-G-A

32760212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104737938-G-C

32760212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104737938-G-T

32760382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737765-T-C

http://identifiers.org/hco/11/GRCh38#32760450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104737697-C-A

32760453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737694-T-A

32760453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737694-T-C

32760482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737665-C-T

32760574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737555-G-A

32760626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737506-G-A

http://identifiers.org/hco/11/GRCh38#32760842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104737285-C-A

32760890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737240-G-A

http://identifiers.org/hco/11/GRCh38#32760894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104737236-A-C

32760894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737236-A-G

32760899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737231-T-C

32760907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737223-T-C

32760932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104737198-G-A

32786989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104724639-G-A

http://identifiers.org/hco/11/GRCh38#32787794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104723824-C-A

http://identifiers.org/hco/11/GRCh38#32787956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104723513-A-C

32787956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104723513-A-T

32788104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104723395-C-G

http://identifiers.org/hco/11/GRCh38#32788258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104723241-A-C

32789652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104720498-A-G

32790518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104720147-A-G

32790760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104719971-T-C

32792199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104719629-A-G

32792534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104719069-T-C

http://identifiers.org/hco/11/GRCh38#32792570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104719033-C-A

32792570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104719033-C-G

32792570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104719033-C-T

http://identifiers.org/hco/11/GRCh38#32792799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104718677-C-A

32792799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104718677-C-T

32793115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104718377-A-G

32793192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104718319-A-G

http://identifiers.org/hco/11/GRCh38#32793679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104717756-A-C

32793679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717756-A-T

32793831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717581-A-G

32793847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717550-G-A

32793868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717526-C-T

32794000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717432-A-G

32794035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104717286-G-A

32794237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716975-G-A

32794237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716975-G-T

32794239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716973-A-G

32794270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716945-A-G

32794279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716936-C-T

32794286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716929-A-G

http://identifiers.org/hco/11/GRCh38#32794339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104716891-C-A

32794339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104716891-C-T

32794371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716879-G-A

32794415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716859-T-C

http://identifiers.org/hco/11/GRCh38#32794416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104716858-C-A

32794416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716858-C-T

32794465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716820-G-A

32794524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716766-A-G

32794573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716719-T-C

http://identifiers.org/hco/11/GRCh38#32794577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104716715-C-A

32794577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716715-C-T

32794588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 104716704-C-T

32794606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104716697-G-A

32794629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104716674-T-C

32794641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104716667-T-A

32794641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104716667-T-C

32794732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 104716583-G-A

http://identifiers.org/hco/11/GRCh38#32794931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104716351-C-A

http://identifiers.org/hco/11/GRCh38#32795063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104716207-C-A

32829732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104680225-G-A

32829732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104680225-G-T

32829770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: 104680201-G-T

32829802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104680179-G-A

32829802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 104680179-G-T

32829898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, undefined
orthologous variants: 104680150-G-C

32829898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron_variant, undefined
orthologous variants: 104680150-G-T

http://identifiers.org/hco/11/GRCh38#32829921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23261
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#104680137-C-A