64459726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735944-T-C

64459860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735824-G-T

http://identifiers.org/hco/15/GRCh38#64460123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65735415-A-C

64460123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65735415-A-G

64460473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65735107-A-G

64460606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65734974-G-A

64460606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65734974-G-T

64460609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65734971-G-A

64460609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 65734971-G-T

64460773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734811-A-G

64460776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734808-G-A

64460776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734808-G-T

http://identifiers.org/hco/15/GRCh38#64460778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65734806-C-A

64460778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734806-C-T

http://identifiers.org/hco/15/GRCh38#64460783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65734801-C-A

64460783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734801-C-T

http://identifiers.org/hco/15/GRCh38#64460910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#65734680-C-A

http://identifiers.org/hco/15/GRCh38#64460960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65734635-A-C

64461118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65734482-G-A

64461233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65734389-G-A

64461233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65734389-G-T

64462854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65732826-C-G

http://identifiers.org/hco/15/GRCh38#64463451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65732470-C-A

64463567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65732371-A-G

64463775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65732162-T-G

64463860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65732080-T-A

64463933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65732014-C-G

64464017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65731932-G-A

64464247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65731723-C-T

64464940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65731051-A-G

64465040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65730969-C-G

64465040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65730969-C-T

64465370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65730652-A-G

64466296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65730068-C-G

64466440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65729933-C-T

64466693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65729737-G-C

64467085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65729499-A-T

64467215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65729217-C-G

http://identifiers.org/hco/15/GRCh38#64467263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65729175-C-A

64467263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65729175-C-G

64472316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65728968-A-G

64474586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65727474-A-G

64474586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65727474-A-T

64475146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65726282-C-G

http://identifiers.org/hco/15/GRCh38#64475241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65726219-C-A

64475241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65726219-C-T

64476529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65724930-C-T

64476695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65724783-C-T

64477489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: -A-T

64478039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65723409-C-T

64478739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65722938-C-T

64484413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65720929-C-T

64484471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65720873-T-A

64486871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65713233-A-T

64487074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65713041-G-T

64487293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65712843-T-A

64487293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65712843-T-C

64490662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710845-T-G

http://identifiers.org/hco/15/GRCh38#64490734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65710787-C-A

64490807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710712-A-G

64490808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710711-G-A

64490870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710649-T-A

64490872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710647-G-A

64491048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710476-C-T

64491225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65710295-T-C

64493013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65708052-C-G

http://identifiers.org/hco/15/GRCh38#64493044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65708021-A-C

64493148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65707932-G-A

64493219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65707870-A-T

64493801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65707351-T-G

64493907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65707247-G-T

64495906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65705320-C-T

http://identifiers.org/hco/15/GRCh38#64496446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65704813-A-C

64496446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704813-A-G

64497056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704338-T-C

64497374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704151-G-T

64497410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704107-C-G

64497410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704107-C-T

64497412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704103-C-T

64497416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65704099-T-C

64498710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65703352-C-T

64499156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65702911-A-G

64500187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, stop_gained
orthologous variants: 65701881-G-A

http://identifiers.org/hco/15/GRCh38#64500216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65701856-C-A

64500216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, missense_variant
orthologous variants: 65701856-C-G

64500753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65701319-T-A

64500986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65701094-T-C

64501016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65701064-T-C

http://identifiers.org/hco/15/GRCh38#64501391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65700676-C-A

http://identifiers.org/hco/15/GRCh38#64501462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65700602-C-A

64501505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700559-T-C

64501515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700549-T-C

64501547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700517-C-T

64501598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700466-T-C

64501651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700414-T-C

http://identifiers.org/hco/15/GRCh38#64501697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65700369-C-A

64501697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700369-C-T

64502070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700051-G-T

64502099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700022-A-G

64502099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 65700022-A-T

64502444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65699266-A-G

64503089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698664-T-C

64503148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698607-C-T

64503381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698426-G-C

64503381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698426-G-T

64503671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698141-G-C

64503761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698060-T-C

64503794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698029-C-T

64503813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65698006-C-T

http://identifiers.org/hco/15/GRCh38#64503836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65697980-A-C

64503859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65697957-C-G

64503859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65697957-C-T

64504194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65697653-A-G

64504345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65697497-A-G

64506885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65695467-A-G

64507808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694567-C-G

64507995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694380-C-G

64507995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694380-C-T

64508080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65694272-T-C

64508508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65693698-G-C

64512217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690312-C-G

64512294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65690145-A-G

64512532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689898-A-G

64513000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689223-G-A

64513000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65689223-G-C

64513390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65688841-G-C

64520632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65685056-T-C

64520861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684870-G-A

64521368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684427-T-A

64521593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684283-C-G

64521593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684283-C-T

64521630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684246-T-C

64521630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65684246-T-G

64521904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65683709-T-C

64522366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65682642-T-C

64522989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65681717-A-T

http://identifiers.org/hco/15/GRCh38#64530819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65680047-C-A

64531076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679701-C-G

64531080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679697-T-G

64531097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679680-C-T

64531642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679223-C-G

64531847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679080-A-G

64532721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65678069-A-G

64543286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65676024-T-A

http://identifiers.org/hco/15/GRCh38#64545054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65674326-A-C

64545165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65674028-T-C

64545502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65673954-A-G

64546049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65673462-G-A

64546067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65673444-G-A

64546067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65673444-G-C

64559136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65671696-A-G

64559473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65671233-G-A

64559514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65671096-T-G

64559632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670911-G-A

64559677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670865-A-G

64559693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670841-A-G

64559822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670714-T-G

64559876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670662-G-A

64560554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670309-C-G

64560554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65670309-C-T

64561072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65669347-C-T

64564542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668283-A-T

64564561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65668262-C-T

64566804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65666858-T-C

64567135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65666117-G-A

64567153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65666099-T-G

http://identifiers.org/hco/15/GRCh38#64574061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65664035-A-C

64574467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663702-C-T

64574585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663585-A-G

64574586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663584-T-C

64575144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65663026-A-T

64589405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65655417-G-C

http://identifiers.org/hco/15/GRCh38#64589431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65655390-A-C

64589536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65655301-T-A

64589915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65654993-C-T

64590095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65654680-C-T

64596711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65652326-C-T

64601633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65649730-G-C

64603794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65647941-T-A

64615721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644841-A-G

64615803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644760-C-T

64616031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644643-T-G

64616097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644579-C-G

64616141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644526-A-G

64616194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644402-A-G

64616494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644034-A-T

64616496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65644032-A-T

64619413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65643426-C-T

64620113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65641980-G-A

64620388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65641560-A-G

64620946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65640591-T-G

64621109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65640428-G-A

64621170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65640387-A-T

64621933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65639544-T-C

http://identifiers.org/hco/15/GRCh38#64622046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65639457-A-C

64622046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65639457-A-G

64622470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65639062-C-G

64622565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65638776-A-G

64622603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65638692-T-C

http://identifiers.org/hco/15/GRCh38#64623107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65638215-C-A

64623198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65638081-T-G

64623342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65637884-A-G

64623521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65637197-T-C

64627352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65635978-A-T

64634285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65633891-T-G

64634309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65633877-A-G

64634309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65633877-A-T

64634355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65633838-G-A

64634807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65633501-T-C

64634854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65633454-T-C

http://identifiers.org/hco/15/GRCh38#64634899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#65633409-A-C

64635458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65632698-G-T

64635475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65632682-T-G

64635589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65632568-G-A

64635715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65632438-C-G

http://identifiers.org/hco/15/GRCh38#64636331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65631785-A-C

64636331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65631785-A-G

http://identifiers.org/hco/15/GRCh38#64636652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65631413-A-C

64637010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65631078-A-G

64637107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65631019-C-T

64637417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65630600-A-G

64637432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65630584-A-T

http://identifiers.org/hco/15/GRCh38#64637518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65630395-C-A

64637813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65630111-A-G

64637971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65629957-A-T

64640556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65628850-A-G

64640745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65628670-A-G

64643239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 65627320-C-T

64643466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65627095-T-C

64647794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65625678-C-G

64648040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65625443-C-T

64648669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65625103-G-A

64648669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65625103-G-T

64652411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65623366-G-T

64652433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65623344-C-T

64652779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65623097-T-C

64653297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622455-G-A

64653335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622419-T-A

64653370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622357-C-T

64653449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622275-A-G

64653463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622261-G-A

64653636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622099-A-G

64653637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65622098-C-T

64653765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65621973-T-G

http://identifiers.org/hco/15/GRCh38#64653838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65621910-C-A

64654003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65621556-G-T

64656850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65618522-C-T

http://identifiers.org/hco/15/GRCh38#64664529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65616867-A-C

64665283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65616171-T-C

64665338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65616120-G-A

64669821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65614466-C-T

64670025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65613752-C-G

64670025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65613752-C-T

64670441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65613363-C-G

64670441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 65613363-C-T

64673893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65611921-T-C

64674146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65611668-A-G

http://identifiers.org/hco/15/GRCh38#64674603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65611214-C-A

64674928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610889-G-A

64674928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610889-G-T

64674991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610826-G-A

64674991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610826-G-C

http://identifiers.org/hco/15/GRCh38#64675061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65610756-A-C

64675079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610738-A-G

64675204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: stop gained
orthologous variants: 65610613-C-T

64675351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610466-G-A

64675420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610397-G-A

http://identifiers.org/hco/15/GRCh38#64675486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65610331-A-C

64675596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: synonymous variant
orthologous variants: 65610221-C-T

64675678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65610139-G-A

64675768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: synonymous variant
orthologous variants: 65610049-C-T

64675947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: synonymous variant
orthologous variants: 65609861-G-A

64676110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65609698-T-C

64676303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65609507-C-G

64676303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65609507-C-T

64676359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65609452-T-G

64676388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65609423-T-C

64677676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608995-C-G

64678012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608562-T-A

http://identifiers.org/hco/15/GRCh38#64678019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65608560-C-A

64678019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608560-C-G

64678019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608560-C-T

64678527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608062-A-G

64678540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65608051-T-C

64678903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65607706-G-A

64678944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65607665-A-G

64679095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65607477-G-A

64679378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65607166-T-C

64679994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65605109-A-G

64679994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65605109-A-T

64680068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65605057-T-C

64680145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65604987-C-T

64680171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65604963-T-G

64680530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65604612-G-T

64680757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: missense variant
orthologous variants: 65604417-C-T

64680971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65604238-T-C

64680971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65604238-T-G

http://identifiers.org/hco/15/GRCh38#64681394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65603416-C-A

64681394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65603416-C-G

64681394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 65603416-C-T

64681454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65603356-T-A

http://identifiers.org/hco/15/GRCh38#64681472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65603336-C-A

64681472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65603336-C-G

64681492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65603316-G-A

64681492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: 65603316-G-T

http://identifiers.org/hco/15/GRCh38#64681517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65603291-C-A

64681552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, undefined
orthologous variants: 65603258-T-G

64681686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 65602980-T-C

64681777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602889-T-G

64681860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602808-G-A

64681860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602808-G-T

http://identifiers.org/hco/15/GRCh38#64681866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65602803-C-A

64681866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602803-C-T

64682453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602244-G-A

64682453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602244-G-C

64682453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602244-G-T

64682455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602242-G-A

64682472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602225-G-T

64682513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602180-T-C

64682618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65602081-A-G

64683072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601681-T-C

64683077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601676-A-G

64683268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601493-G-T

64683297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601456-G-A

64683297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601456-G-T

64683548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65601237-T-C

http://identifiers.org/hco/15/GRCh38#64683619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65601171-C-A

64683836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600967-G-A

64684247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600536-T-A

64684247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600536-T-G

64684330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600515-A-G

http://identifiers.org/hco/15/GRCh38#64684350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600495-C-A

64684350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600495-C-T

64684414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600431-G-T

http://identifiers.org/hco/15/GRCh38#64684432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600413-C-A

64684432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600413-C-G

http://identifiers.org/hco/15/GRCh38#64684435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600410-A-C

http://identifiers.org/hco/15/GRCh38#64684482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600367-C-A

64684482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600367-C-T

64684660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600237-C-G

64684742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600156-C-T

http://identifiers.org/hco/15/GRCh38#64684771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600132-C-A

http://identifiers.org/hco/15/GRCh38#64684781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600122-C-A

64684782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600121-T-C

http://identifiers.org/hco/15/GRCh38#64684829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600083-C-A

64684829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600083-C-T

http://identifiers.org/hco/15/GRCh38#64684841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65600071-C-A

64684844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600069-A-G

64684844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600069-A-T

64684897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600024-T-C

64684918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65600003-G-T

http://identifiers.org/hco/15/GRCh38#64684957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65599983-C-A

64684957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599983-C-T

64684979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599961-C-T

64684986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599954-T-C

64685001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599939-G-A

64685001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599939-G-T

64685006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599934-C-T

http://identifiers.org/hco/15/GRCh38#64685008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65599932-C-A

64685008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599932-C-T

http://identifiers.org/hco/15/GRCh38#64685039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65599901-C-A

64685039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599901-C-T

64685519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599435-G-T

64685602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599356-T-C

64685690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599263-G-T

64685716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599236-G-T

64685735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599194-A-G

http://identifiers.org/hco/15/GRCh38#64685741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#65599188-C-A

64685741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599188-C-T

64685789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599123-G-T

64685855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65599054-A-G

64685933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65598987-T-C

64685949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29003
most severe consequence: 3 prime UTR variant
orthologous variants: 65598972-A-G