51222365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5 prime UTR variant
orthologous variants: 62793222-G-A

51222365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5 prime UTR variant
orthologous variants: 62793222-G-C

51222375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5 prime UTR variant
orthologous variants: 62793231-T-C

51222375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5 prime UTR variant
orthologous variants: 62793231-T-G

http://identifiers.org/hco/13/GRCh38#51222389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62793244-C-A

51222389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62793244-C-G

51222389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62793244-C-T

http://identifiers.org/hco/13/GRCh38#51222489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62793289-C-A

51222489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62793289-C-T

http://identifiers.org/hco/13/GRCh38#51222645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62793435-C-A

51222645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793435-C-T

http://identifiers.org/hco/13/GRCh38#51222693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62793468-C-A

51222693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793468-C-G

51222693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793468-C-T

http://identifiers.org/hco/13/GRCh38#51222698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62793473-C-A

51222698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793473-C-G

51222698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793473-C-T

51222752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793524-G-A

51222981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62793715-C-T

51223514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794130-G-T

51223587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794203-A-G

http://identifiers.org/hco/13/GRCh38#51223619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62794233-A-C

51223631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794244-C-G

51223845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794561-T-G

51223850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62794566-T-C

51224590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795195-T-C

51224616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795234-G-A

51224771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795342-G-T

51224905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795456-G-A

51224940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62795491-C-T

51225323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62795814-A-G

51226310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796408-G-A

51226551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796585-C-T

51226653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796672-G-T

51226692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796715-A-G

51226904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62796918-T-C

51227183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62797312-A-G

51227300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62797425-G-A

51227356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62797481-G-T

http://identifiers.org/hco/13/GRCh38#51227571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62797660-C-A

51227571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62797660-C-G

51227654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62797742-C-T

51227947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62798003-G-A

51227947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62798003-G-T

51228512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62798900-G-A

51228953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62799412-G-T

51229219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62799676-G-C

51229286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62799740-A-G

51229340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62799785-G-A

51229709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62800127-C-T

http://identifiers.org/hco/13/GRCh38#51229728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62800146-A-C

51229728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62800146-A-G

51229934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62800347-T-C

51230040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62800441-T-C

51230595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801245-A-G

51230616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801266-G-A

51230622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801272-C-T

51230719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801371-G-A

51230826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801453-G-A

51231070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801678-A-G

51231197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801781-T-C

http://identifiers.org/hco/13/GRCh38#51231214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62801798-C-A

51231214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801798-C-G

51231223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801804-G-A

51231232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801813-A-T

51231236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62801817-G-T

http://identifiers.org/hco/13/GRCh38#51231251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62801830-C-A

51231387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 62801976-T-C

51231518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62805703-G-C

51231518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62805703-G-T

51231675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62805888-A-G

51231691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62805904-C-G

51232489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806658-G-A

51232489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806658-G-T

51232548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806716-A-T

51232569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806738-C-T

51232810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806943-T-A

51232810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62806943-T-G

51232991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807089-C-T

51233017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807114-G-T

51233052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807142-G-A

51233274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807308-T-C

http://identifiers.org/hco/13/GRCh38#51233318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62807355-C-A

51233318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807355-C-T

51233336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62807373-A-G

51233638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62808001-A-T

51233749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62808090-T-G

51233965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62808303-G-A

51233965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62808303-G-T

51234846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62812087-A-G

51235359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62812642-A-G

51235359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62812642-A-T

51235401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62812685-C-G

51236217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813285-G-T

51236377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813369-T-G

51236438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813435-A-G

http://identifiers.org/hco/13/GRCh38#51236475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62813470-C-A

51236708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813629-A-G

51236758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813680-T-G

51236770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813692-T-G

51237974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62813970-A-T

51238114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814086-C-T

51238196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814145-A-G

51238352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814244-G-A

http://identifiers.org/hco/13/GRCh38#51238489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62814341-A-C

51238491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814343-A-G

51238592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814456-T-G

51238782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814593-G-T

http://identifiers.org/hco/13/GRCh38#51238796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62814605-C-A

51238926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814716-A-G

51239177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62814947-G-C

51239273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815070-G-A

51239696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815444-T-C

51239703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815451-T-A

51239703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815451-T-C

51239832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815569-G-A

51239845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815584-A-G

51239867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815606-G-A

51239869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815608-G-A

51239944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815682-G-C

51239944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815682-G-T

51239961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815699-T-C

51239993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815724-G-A

http://identifiers.org/hco/13/GRCh38#51240030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62815758-C-A

51240291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62815970-G-T

51241125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -A-G

51241138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -T-C

51241202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -C-T

51241215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -G-A

51241234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -C-T

51241260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: -G-A

51241467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62817410-G-A

51241618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62817558-G-A

51241659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62817592-A-T

51241782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62817698-A-G

51241853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818035-G-A

51241871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818053-T-C

http://identifiers.org/hco/13/GRCh38#51241887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62818069-A-C

http://identifiers.org/hco/13/GRCh38#51242045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62818218-C-A

51242048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818221-G-A

51242154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818298-T-G

51242200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818345-T-G

51242209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818354-G-A

51242209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62818354-G-T

51242490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819076-C-G

51242794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819356-T-A

http://identifiers.org/hco/13/GRCh38#51243006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62819558-A-C

51243119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819639-G-A

51243294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819770-G-A

51243294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819770-G-C

51243345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819820-T-C

51243377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62819851-C-T

51244031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820110-A-T

51244177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820199-G-A

51244198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820220-A-G

51244233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820257-C-G

51244233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820257-C-T

51244234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62820258-G-A

51244286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62820302-G-A

51244369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62820374-C-T

51244392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62820390-A-G

51244434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62820427-A-G

51244848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62820821-C-T

51245723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821378-T-G

51245947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821600-G-A

51246208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821842-C-T

51246248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821883-A-G

51246249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821884-T-C

51246306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62821938-A-G

51246385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822017-A-G

51246386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822018-G-T

51246391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822023-G-T

51246412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822024-G-A

51246412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822024-G-C

51246412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62822024-G-T

51247664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823186-G-C

51247713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823233-C-T

51247776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823296-A-G

51247776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823296-A-T

51247872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823371-G-C

51247897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62823395-T-C

51251415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62824357-T-A

51251415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62824357-T-C

51251418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62824360-A-T

51251617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: missense variant
orthologous variants: 62824751-A-T

http://identifiers.org/hco/13/GRCh38#51251744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62824878-C-A

51251744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: missense variant
orthologous variants: 62824878-C-T

http://identifiers.org/hco/13/GRCh38#51251982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62825116-C-A

http://identifiers.org/hco/13/GRCh38#51252045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62825179-C-A

51252045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: synonymous variant
orthologous variants: 62825179-C-T

51252399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825520-G-A

51252399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825520-G-C

51252399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825520-G-T

51252419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825554-A-G

51252665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825775-G-A

51252665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825775-G-T

51252689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825799-G-A

http://identifiers.org/hco/13/GRCh38#51252708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62825821-C-A

http://identifiers.org/hco/13/GRCh38#51252721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62825834-C-A

51252736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825837-A-G

51253366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825871-T-G

51253470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825964-G-A

51253470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825964-G-T

51253503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62825994-T-G

http://identifiers.org/hco/13/GRCh38#51253537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62826027-C-A

51253537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62826027-C-T

51253543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62826033-A-G

http://identifiers.org/hco/13/GRCh38#51253606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62826093-C-A

51253606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 62826093-C-T

51253863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826306-G-T

51253893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826346-T-C

http://identifiers.org/hco/13/GRCh38#51253900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62826353-A-C

51253900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826353-A-G

51253981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826394-C-G

51253981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826394-C-T

51254104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826521-G-A

51254104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826521-G-C

51254104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62826521-G-T

51266906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62828849-T-A

51266906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62828849-T-C

51267083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62829012-C-T

51267141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62829073-C-T

51267437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62829382-A-G

51267623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62829548-G-T

51267892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62829916-G-A

51268103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62830150-T-C

51268134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62830176-A-G

51268490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62834121-G-A

51269805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62835773-T-C

51269917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62835876-G-C

51269969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62835951-C-T

http://identifiers.org/hco/13/GRCh38#51269977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62835959-C-A

51270041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62836017-G-A

51270897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62836507-T-C

51270996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron_variant, undefined
orthologous variants: 62836601-A-G

51271092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62836677-A-G

51271202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62836909-C-T

51271359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837091-G-A

51271838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837568-C-T

51271867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837598-C-T

51271918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837647-G-A

51271955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837664-T-G

51272326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62837996-G-T

51272404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62838092-G-A

http://identifiers.org/hco/13/GRCh38#51272443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62838148-C-A

51272501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62838217-A-G

51278044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62839897-T-G

51278100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62839953-G-A

51278165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62840024-G-A

51278682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62840481-G-A

51278924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62840709-C-T

51278940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62840725-C-T

51279044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62840821-A-G

51279562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62842079-G-A

51279685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62842189-G-A

51280377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62843246-T-C

51280398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62843266-G-A

51280398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: intron variant
orthologous variants: 62843266-G-T

51280504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843376-G-A

51280536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 62843408-C-T

51280573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 62843445-C-T

51280871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843719-G-A

51280928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843776-G-T

51280981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843829-G-A

http://identifiers.org/hco/13/GRCh38#51281014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62843862-A-C

51281014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843862-A-T

51281105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843953-C-T

51281150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62843998-A-G

http://identifiers.org/hco/13/GRCh38#51281204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62844052-C-A

51281215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 62844063-G-A

51281260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844108-C-T

51281338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844187-A-G

51281430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844295-A-G

51281440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844502-T-C

http://identifiers.org/hco/13/GRCh38#51281461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62844528-A-C

http://identifiers.org/hco/13/GRCh38#51281471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62844538-C-A

51281471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844538-C-T

http://identifiers.org/hco/13/GRCh38#51281538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62844582-A-C

51281684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844721-A-T

51281712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844748-T-G

51281814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844839-A-G

51281832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844855-T-C

51281832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844855-T-G

51281962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62844987-A-T

51282111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845119-A-G

51282113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845121-T-C

http://identifiers.org/hco/13/GRCh38#51282192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845208-C-A

51282192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845208-C-T

http://identifiers.org/hco/13/GRCh38#51282206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845221-C-A

51282206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845221-C-T

http://identifiers.org/hco/13/GRCh38#51282258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845257-C-A

http://identifiers.org/hco/13/GRCh38#51282369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845351-A-C

51282369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845351-A-G

51282427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845408-G-A

http://identifiers.org/hco/13/GRCh38#51282477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845444-A-C

51282536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845499-G-A

51282536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845499-G-T

51282562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845525-A-G

51282567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845530-C-T

51282568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845531-C-T

51282570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845533-T-C

51282687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845629-A-G

51282727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845663-A-T

51282785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845715-G-A

51282785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845715-G-C

51282785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845715-G-T

http://identifiers.org/hco/13/GRCh38#51282792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#62845722-C-A

51282835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845749-T-C

51282869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845778-T-C

51283382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62845989-G-A

51283629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846148-G-T

51283632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846151-A-G

51283740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846257-G-A

51283815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846314-G-A

51283885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846381-G-T

51283947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846474-A-G

51284003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846527-G-A

51284012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846536-G-A

51284059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846567-G-C

51284059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846567-G-T

51284092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26413
most severe consequence: 3 prime UTR variant
orthologous variants: 62846602-C-T