http://identifiers.org/hco/15/GRCh38#51341708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54193831-C-A

51341708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54193831-C-T

51341715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: 54193838-G-A

51341715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: 54193838-G-C

51341715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: 54193838-G-T

51341795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54193918-G-A

51341795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54193918-G-T

http://identifiers.org/hco/15/GRCh38#51341796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54193919-C-A

51341796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54193919-C-T

51341814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54193937-C-T

http://identifiers.org/hco/15/GRCh38#51341880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54194003-C-A

51341880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54194003-C-T

51341881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54194004-G-C

51341881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54194004-G-T

51341912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194035-G-A

51341912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194035-G-C

51341912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194035-G-T

http://identifiers.org/hco/15/GRCh38#51341975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54194098-C-A

51341975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194098-C-T

51342002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194125-C-G

51342002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54194125-C-T

51342180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54194288-G-T

51342202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54194310-G-A

51342202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54194310-G-T

51342398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54194482-G-A

http://identifiers.org/hco/15/GRCh38#51343092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54195342-A-C

51343144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54195392-A-G

51343363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54195608-A-T

51343418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54195663-G-T

51343653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54195860-T-C

51343695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54195904-G-A

51344107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196346-C-T

51344111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196350-T-C

51344122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196361-T-C

51344250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196492-G-A

http://identifiers.org/hco/15/GRCh38#51344312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54196561-C-A

http://identifiers.org/hco/15/GRCh38#51344495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54196733-A-C

51344495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196733-A-G

51344541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196793-A-G

51344601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196857-C-G

51344730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54196991-T-C

51344843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54197085-A-T

51345016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54197220-T-C

http://identifiers.org/hco/15/GRCh38#51345019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54197223-A-C

51345137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54197344-C-T

51345172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54197386-C-T

51348801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54206862-C-G

51350293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54207445-T-G

51350414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54207552-C-G

51350435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54207573-A-G

51350589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54207694-G-A

51350766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54208571-G-T

51350838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54208639-G-A

http://identifiers.org/hco/15/GRCh38#51350962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54208779-C-A

51351026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54208837-G-T

51351449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54208904-G-T

51351975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54209330-A-G

51352284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210131-A-G

51352306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210153-T-C

51352588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210410-G-T

http://identifiers.org/hco/15/GRCh38#51352638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54210458-A-C

http://identifiers.org/hco/15/GRCh38#51353591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54210802-A-C

51353687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210913-A-G

51353689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210915-T-A

51353741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210946-T-A

51353741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210946-T-C

51353741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210946-T-G

51353761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210981-G-A

51353761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210981-G-C

51353761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54210981-G-T

51353812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54211028-C-T

51354686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54211942-G-A

51354959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54212196-T-C

51356539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54212469-T-C

51368923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

51368924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

51368929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

51368948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

51368952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

51369009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#51369315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

51373673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215667-G-A

51373749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215708-C-T

51373829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215782-C-T

51373894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54215846-A-G

51374493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54216459-C-G

51375163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217131-T-C

51375205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217171-A-G

51375256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217430-A-G

51375344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217515-A-G

51375480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217628-T-G

51375525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217655-T-C

51375758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54217843-T-G

51377322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220049-G-A

51377322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220049-G-T

http://identifiers.org/hco/15/GRCh38#51377377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54220104-C-A

51377377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220104-C-T

51377380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220107-G-A

51377380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220107-G-C

51377380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54220107-G-T

http://identifiers.org/hco/15/GRCh38#51377399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54220127-C-A

51377565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54220291-A-G

51377648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54220372-T-C

51377946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221489-C-G

51377994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221534-A-G

51378085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221626-A-T

51378169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221693-T-C

51378327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221830-G-A

51378327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54221830-G-T

51378611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222111-A-G

51378659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54222150-T-A

51380857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223305-C-T

51381155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223591-C-T

51381221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54223655-G-A

51381413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54223833-C-T

51381438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54223862-G-A

51381769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226359-T-A

51381769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226359-T-G

51381772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226362-T-C

51381772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226362-T-G

51381946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226508-G-A

51382013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226572-G-A

http://identifiers.org/hco/15/GRCh38#51382035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54226586-A-C

51382035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226586-A-G

51382307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226860-G-C

51382307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226860-G-T

51382356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226908-G-A

51382666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226986-C-T

51382675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226995-G-A

51382675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54226995-G-T

http://identifiers.org/hco/15/GRCh38#51382755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54227002-C-A

51382755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227002-C-G

51382755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227002-C-T

51382788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227036-A-G

51382798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227046-C-T

51382811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227059-T-C

51382814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227062-A-T

51382854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227124-T-C

51382916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54227186-C-T

51382918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54227188-G-A

51382994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54227264-C-G

51383146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227418-C-T

51383324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227597-T-G

51383352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227619-A-G

51383355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227622-T-A

http://identifiers.org/hco/15/GRCh38#51383371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54227649-C-A

51383371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227649-C-G

51383371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227649-C-T

51383398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227676-G-A

51383398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227676-G-T

51383495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227770-G-C

http://identifiers.org/hco/15/GRCh38#51383505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54227780-C-A

51383629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227938-T-A

51383668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227974-T-G

51383671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227977-G-A

51383671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54227977-G-T

http://identifiers.org/hco/15/GRCh38#51383699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228003-C-A

51383699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228003-C-G

51383699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228003-C-T

51383709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54228014-G-T

http://identifiers.org/hco/15/GRCh38#51383782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228069-C-A

51383782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54228069-C-T

51383798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54228085-C-T

51383801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54228088-C-T

51383834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54228121-G-A

51383912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54228198-T-A

51383913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54228199-A-G

51383939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228225-A-G

51383941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228227-G-T

51383943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228229-T-C

51384028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228316-A-G

51384028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228316-A-T

51384036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228324-T-C

51384036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228324-T-G

51384064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228351-T-C

51384101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228380-G-T

51384104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228383-A-G

51384124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228403-A-G

http://identifiers.org/hco/15/GRCh38#51384191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228439-C-A

51384235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228476-G-A

51384235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228476-G-C

51384235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228476-G-T

51384240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228481-G-C

51384240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228481-G-T

51384245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228488-T-C

51384260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228502-T-C

51384276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228514-G-A

51384276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228514-G-T

51384316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228545-G-A

51384316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228545-G-T

http://identifiers.org/hco/15/GRCh38#51384371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228597-A-C

51384371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228597-A-G

51384371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228597-A-T

http://identifiers.org/hco/15/GRCh38#51384422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228646-C-A

51384468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228682-A-G

51384473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228687-C-T

51384485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228699-T-C

51384487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228701-T-C

51384578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228769-A-G

http://identifiers.org/hco/15/GRCh38#51384583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228774-C-A

51384593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228784-G-A

51384593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228784-G-C

51384593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228784-G-T

http://identifiers.org/hco/15/GRCh38#51384594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228785-C-A

51384594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228785-C-T

51384643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228826-G-A

51384643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228826-G-T

51384689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228879-T-C

http://identifiers.org/hco/15/GRCh38#51384772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54228942-C-A

51384773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228943-A-G

51384783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54228955-G-T

51384881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229027-A-G

51384931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229100-C-T

51384940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229109-T-C

51384956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229125-T-C

51384961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229130-T-C

http://identifiers.org/hco/15/GRCh38#51385061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54229230-C-A

51385061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229230-C-T

51385105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229274-T-A

51385105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229274-T-C

51385277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229434-A-G

http://identifiers.org/hco/15/GRCh38#51385281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54229438-C-A

51385281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229438-C-T

51385308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229466-C-T

51385322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229479-G-A

51385322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229479-G-T

http://identifiers.org/hco/15/GRCh38#51385379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54229541-C-A

http://identifiers.org/hco/15/GRCh38#51385388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54229545-C-A

51385414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229571-A-G

51385445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54229602-G-A

51386326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230317-A-G

51386532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230483-G-A

51386581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230517-G-A

51386644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230573-G-C

51386769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230674-G-A

51386914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54230777-C-T

http://identifiers.org/hco/15/GRCh38#51387261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54231113-A-C

51387346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54231186-T-C

51387347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54231187-C-G

51389683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54231991-G-A

51389758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54232004-G-A

51389758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54232004-G-T

51389767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54232013-G-C

51389837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54232086-G-A

51390443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54234125-T-A

51390443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54234125-T-G

51390900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, undefined
orthologous variants: 54234570-T-C

51390957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54234619-C-T

51391281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, undefined
orthologous variants: 54235836-C-T

51391329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, undefined
orthologous variants: 54235889-A-G

51391741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54236263-C-G

51394709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239049-T-C

51394753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239091-A-T

51394799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239131-A-G

51394817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239146-T-C

51394956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54239282-T-C

http://identifiers.org/hco/15/GRCh38#51394968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54239294-C-A

51394968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54239294-C-T

http://identifiers.org/hco/15/GRCh38#51395044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54239355-C-A

51395062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239372-T-C

51395104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239404-G-T

51395111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54239411-G-T

51397384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240404-T-C

http://identifiers.org/hco/15/GRCh38#51397388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240408-C-A

51397388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240408-C-G

51397388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240408-C-T

http://identifiers.org/hco/15/GRCh38#51397410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240430-C-A

51397410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240430-C-G

51397410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240430-C-T

51397430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240453-T-A

51397430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240453-T-C

http://identifiers.org/hco/15/GRCh38#51397431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240454-C-A

51397431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240454-C-G

51397431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240454-C-T

http://identifiers.org/hco/15/GRCh38#51397442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240465-C-A

51397442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240465-C-G

51397442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240465-C-T

http://identifiers.org/hco/15/GRCh38#51397489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240506-C-A

51397489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54240506-C-T

http://identifiers.org/hco/15/GRCh38#51397510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240527-C-A

51397510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54240527-C-G

51397510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54240527-C-T

http://identifiers.org/hco/15/GRCh38#51397601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240609-C-A

51397676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240673-A-G

51397723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240709-G-T

http://identifiers.org/hco/15/GRCh38#51397746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240730-C-A

51397746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240730-C-G

51397746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54240730-C-T

http://identifiers.org/hco/15/GRCh38#51397810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54240793-A-C

http://identifiers.org/hco/15/GRCh38#51400079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54241601-A-C

51400137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54241649-A-G

51400256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54241754-A-G

51400467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54242034-T-C

51400467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: missense variant
orthologous variants: 54242034-T-G

51400583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242133-G-A

http://identifiers.org/hco/15/GRCh38#51400640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54242187-C-A

51400640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242187-C-T

51400717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242265-G-A

51400908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242528-C-G

51400908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242528-C-T

51401335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242934-G-A

51401335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242934-G-T

http://identifiers.org/hco/15/GRCh38#51401458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54242974-C-A

51401458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54242974-C-T

51401675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: synonymous variant
orthologous variants: 54243120-T-C

http://identifiers.org/hco/15/GRCh38#51401750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54243195-C-A

51401750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 54243195-C-G

51401750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 54243195-C-T

51401754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54243226-C-G

51401890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54243345-T-A

51401905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54243360-A-G

51403174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54244025-C-T

51403365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54244176-G-C

51403482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54244301-G-A

51403482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54244301-G-C

51403543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54244359-T-C

51404072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54245072-A-G

51404198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54245193-T-G

http://identifiers.org/hco/15/GRCh38#51404250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54245592-C-A

51404266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54245606-G-T

51404281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, missense_variant
orthologous variants: 54245624-G-C

51404281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, stop_gained
orthologous variants: 54245624-G-T

51404328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 54245671-G-A

51404572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, missense_variant
orthologous variants: 54245915-G-A

51404572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron_variant, missense_variant
orthologous variants: 54245915-G-T

http://identifiers.org/hco/15/GRCh38#51404766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54246109-C-A

51404766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246109-C-T

51404896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246257-T-A

51404932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246293-T-A

51404932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246293-T-C

51404944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246305-A-G

51404986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246347-G-T

51404987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246348-G-T

http://identifiers.org/hco/15/GRCh38#51404988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54246349-C-A

51404988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246349-C-T

51405208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246538-G-A

51405208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246538-G-C

51405208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246538-G-T

http://identifiers.org/hco/15/GRCh38#51405246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54246575-A-C

51405459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246733-C-T

http://identifiers.org/hco/15/GRCh38#51405641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54246810-A-C

51405670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246836-G-T

51405813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54246992-T-C

51405855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247017-G-T

51405867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247028-C-T

51405928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247061-G-A

51405928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247061-G-T

http://identifiers.org/hco/15/GRCh38#51405954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54247086-C-A

51405954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247086-C-T

51406060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247202-C-T

51406193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247326-T-G

51406224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247352-A-G

51406413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247521-A-G

http://identifiers.org/hco/15/GRCh38#51406662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54247590-A-C

51406709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247633-G-A

51406743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247667-G-A

51406743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54247667-G-T

http://identifiers.org/hco/15/GRCh38#51406939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54247859-C-A

51407053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248095-G-A

51407069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248146-T-C

51407107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248192-G-A

51407139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248230-A-T

51407176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248291-T-C

51407182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248297-A-G

51407383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248480-G-A

51407383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248480-G-T

51407766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248857-G-A

51407766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248857-G-T

51407828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248927-G-C

51407837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248936-G-A

51407837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248936-G-T

http://identifiers.org/hco/15/GRCh38#51407844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54248943-C-A

51407847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54248946-T-C

51408025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54249090-T-C

51408048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54249114-A-G

51408143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29514
most severe consequence: intron variant
orthologous variants: 54249210-A-G