148384107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62681670-G-T

148384944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62681214-C-T

148385042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62681109-A-G

http://identifiers.org/hco/5/GRCh38#148385197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62680943-C-A

148385229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62680911-T-C

148385244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62680899-C-G

148385244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62680899-C-T

148385851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62679873-A-G

http://identifiers.org/hco/5/GRCh38#148386010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62679058-A-C

148386035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62679033-A-T

148386370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62678737-T-C

148386388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62678721-T-C

148386599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62678551-G-T

148390335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677835-A-G

148390469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677629-T-C

148390469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677629-T-G

148390541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677556-T-A

148390626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677473-T-G

148390768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677356-T-G

148390785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677338-A-G

148390948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62677121-T-G

148391101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62676830-C-T

http://identifiers.org/hco/5/GRCh38#148391144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62676800-C-A

148391535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62676460-A-G

148391887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62676121-G-A

148391902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62676118-A-G

148392075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62675996-A-G

148392172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62675900-T-C

148392279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62675790-C-T

http://identifiers.org/hco/5/GRCh38#148392281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62675788-C-A

http://identifiers.org/hco/5/GRCh38#148392341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62675734-A-C

148392357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62675714-A-G

148394144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62674732-C-T

148394379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62674398-C-T

148394413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62674363-T-G

148394432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62674339-G-A

http://identifiers.org/hco/5/GRCh38#148394461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62674310-A-C

148394663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62674182-T-G

148394714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 62674115-G-A

http://identifiers.org/hco/5/GRCh38#148394786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62674068-C-A

148394786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 62674068-C-T

http://identifiers.org/hco/5/GRCh38#148394897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62673957-A-C

148394897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62673957-A-G

148394913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673941-G-A

148394913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673941-G-T

http://identifiers.org/hco/5/GRCh38#148394994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62673886-A-C

148394994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673886-A-G

148395683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673453-A-G

148395693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673441-C-T

http://identifiers.org/hco/5/GRCh38#148395950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62673162-A-C

148395950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673162-A-G

148395950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673162-A-T

148396066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673048-T-A

148396074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673040-T-C

148396096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62673016-A-G

http://identifiers.org/hco/5/GRCh38#148396462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62672643-C-A

148396511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62672591-A-G

148397056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62672266-C-G

148397056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62672266-C-T

148397237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62672036-A-G

148397450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62671846-C-T

148397680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62671627-T-C

148397763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62671569-T-C

148399181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62669139-G-T

148399203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62669116-T-C

148399878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668642-T-C

148400133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668441-T-G

148400352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668244-A-T

148400403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668221-C-T

148400412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668212-A-G

148400423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668201-A-G

148400484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668141-G-A

148400554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668077-A-G

http://identifiers.org/hco/5/GRCh38#148400628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62668009-A-C

148400629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668008-C-G

148400629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62668008-C-T

148401433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62667358-G-A

148401828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62667248-T-C

148401975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62667140-T-G

148401977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62667138-C-T

148402071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 62667044-C-T

148402187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62666927-G-T

148402275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62666817-A-G

148402591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62666504-G-A

148402591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62666504-G-C

148402614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62666481-T-C

148403654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664624-C-G

148403810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664568-A-G

148404209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664308-C-G

148404313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664206-C-T

148404337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664181-T-C

148404366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664152-T-C

148404487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664082-T-C

148404489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62664080-A-G

148404578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663993-A-G

148404648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663923-T-C

http://identifiers.org/hco/5/GRCh38#148404874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62663719-C-A

148404874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663719-C-T

148404967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663638-T-C

148404994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663617-G-A

148405595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663373-T-A

148405595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663373-T-G

148405596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663372-G-C

http://identifiers.org/hco/5/GRCh38#148405599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62663369-C-A

148405604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663364-G-T

148405654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663332-G-T

148405957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663038-G-C

148405957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663038-G-T

148405983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62663009-C-T

148406107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662889-T-C

148406107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662889-T-G

http://identifiers.org/hco/5/GRCh38#148406109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62662888-C-A

148406109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662888-C-G

148406136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662862-G-A

http://identifiers.org/hco/5/GRCh38#148406193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62662827-C-A

148406193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662827-C-T

148406551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662460-A-G

148406729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662297-T-C

148406774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62662253-T-C

http://identifiers.org/hco/5/GRCh38#148407059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62661970-A-C

148407152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661898-A-G

148407184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661865-A-G

148407259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661788-C-T

148408123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661512-G-A

148408123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661512-G-C

148408216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661437-G-A

148408321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661363-G-A

148408355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661332-A-G

148408355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661332-A-T

148408562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661123-C-T

148408595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661093-G-A

148408608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661080-G-A

148408624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661064-A-G

148408656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661041-C-G

148408683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62661026-A-G

http://identifiers.org/hco/5/GRCh38#148409186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62660277-C-A

148409186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62660277-C-T

http://identifiers.org/hco/5/GRCh38#148409226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62660237-C-A

148409233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660230-G-A

148409233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660230-G-T

148409253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660210-G-C

148409256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660207-G-C

148409297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660176-T-A

148409297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660176-T-C

148409298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660175-G-A

148409299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660174-T-G

148409302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660171-G-A

148409302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660171-G-T

148409320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660146-T-A

148409341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660125-T-G

148409421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62660053-T-A

148409641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659859-C-T

148409818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659688-T-C

148409879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659626-T-C

148410025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659563-A-G

http://identifiers.org/hco/5/GRCh38#148410050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62659539-A-C

http://identifiers.org/hco/5/GRCh38#148410132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62659433-C-A

148410132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659433-C-T

http://identifiers.org/hco/5/GRCh38#148410148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62659416-C-A

148410148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659416-C-T

148410605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659356-C-T

148410690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62659276-C-G

148410815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62659155-T-C

148410815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62659155-T-G

148410861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62659111-T-C

148410865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62659107-A-T

148410911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659065-T-A

148410911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62659065-T-C

148411152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 62658833-G-A

148412363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62657354-T-G

148412400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62657323-A-G

148412619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62657057-C-T

148412620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62657056-C-G

148412771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62656816-A-G

148412938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62656640-C-T

148412980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62656611-C-T

148413204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62656429-T-C

148413242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62656397-G-T

148413286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62656356-G-A

http://identifiers.org/hco/5/GRCh38#148413600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62656070-C-A

148413623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62656030-G-T

148413651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62656003-A-G

148413715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655939-T-C

http://identifiers.org/hco/5/GRCh38#148413792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62655873-C-A

148413792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655873-C-T

148413822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655843-T-A

148413822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655843-T-C

148413822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655843-T-G

148413828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655837-G-A

148413828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655837-G-C

148413828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655837-G-T

148413847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655823-T-C

148413936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655751-T-C

148413957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655731-A-G

148413993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655695-T-C

148413993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655695-T-G

http://identifiers.org/hco/5/GRCh38#148414065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62655647-A-C

http://identifiers.org/hco/5/GRCh38#148414066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62655646-C-A

148414066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655646-C-G

148414116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655603-T-A

148414144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655581-G-A

148414144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62655581-G-T

http://identifiers.org/hco/5/GRCh38#148414460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62655269-A-C

148415168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62654628-T-C

148415781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62654027-G-T

148415896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653921-G-A

148415896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653921-G-T

148415908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653912-T-A

148415908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653912-T-G

148415913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653907-T-C

148415993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62653829-T-C

148415993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62653829-T-G

148416074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653748-A-G

148416078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62653744-A-G

148416407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653446-G-T

148416659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62653351-T-C

148416659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62653351-T-G

http://identifiers.org/hco/5/GRCh38#148416744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62653273-C-A

148416744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653273-C-T

148416754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653263-T-C

148416757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653260-G-A

148416757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653260-G-T

148416798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653221-A-G

148416804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653215-G-A

148416804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653215-G-T

148416946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62653079-A-G

148417223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652804-G-A

148417223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652804-G-T

http://identifiers.org/hco/5/GRCh38#148417267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62652765-C-A

http://identifiers.org/hco/5/GRCh38#148417636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62652547-A-C

148417655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652528-C-G

148417676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652507-T-C

http://identifiers.org/hco/5/GRCh38#148417831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62652350-A-C

148417887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652295-A-G

148417916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652271-C-G

148417944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62652243-G-T

http://identifiers.org/hco/5/GRCh38#148423791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62651865-C-A

148423791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62651865-C-T

148423792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62651864-A-G

148423792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62651864-A-T

148423935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62651736-T-G

148424125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62651553-T-A

148424125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 62651553-T-C

148424159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62651519-C-T

http://identifiers.org/hco/5/GRCh38#148424181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62651498-A-C

148424181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62651498-A-G

148424253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62651443-C-T

148424328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62651344-C-T

148424420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62651270-G-T

http://identifiers.org/hco/5/GRCh38#148424845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62650750-A-C

148424885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62650704-A-G

148425277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62650407-T-A

148425412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62650291-G-A

148425412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62650291-G-T

148425702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 62650032-G-A

148425742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649995-T-C

148425781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649945-G-A

http://identifiers.org/hco/5/GRCh38#148425849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62649902-C-A

148425858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649893-G-T

148426014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649682-G-A

148426105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649602-T-C

148426134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649589-A-G

148426253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62649474-C-T

http://identifiers.org/hco/5/GRCh38#148426779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62648956-A-C

148426779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648956-A-G

148426960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648819-C-T

148426972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648807-A-G

148427038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648754-T-C

http://identifiers.org/hco/5/GRCh38#148427080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62648719-C-A

148427080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648719-C-G

148427080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62648719-C-T

148427260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 62648563-C-T

148427262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62648561-G-A

148427262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62648561-G-T

148427359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant
orthologous variants: 62648464-A-G

148427435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant
orthologous variants: 62648376-A-G

148427475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 62648336-T-C

http://identifiers.org/hco/5/GRCh38#148427509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62648302-C-A

148427692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62648119-A-G

148427981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647830-G-C

148427981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647830-G-T

148427998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647813-G-A

148427998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647813-G-C

148427998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647813-G-T

148428108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647699-G-T

148428223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647595-C-T

148428503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647329-A-G

148428640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647226-G-C

148428773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62647099-G-A

148428958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646923-T-C

148429066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646819-A-G

148429074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646816-G-T

148429151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646749-G-A

148429161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646739-A-G

148429251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646665-G-A

148429251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646665-G-T

148429683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646548-T-C

148429771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646454-C-T

148429795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646434-T-G

148430039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646200-A-G

http://identifiers.org/hco/5/GRCh38#148430961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62646057-C-A

148430961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646057-C-G

148430961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62646057-C-T

148431325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62645761-T-A

148431552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62645581-T-A

148431573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62645559-G-A

148431748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62645421-T-A

148432211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62645161-C-T

148432428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644978-T-C

148432568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644866-G-A

148432568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644866-G-T

148432614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644821-A-G

148432657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644796-G-C

148432885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644615-T-C

148432920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644585-T-C

148433060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644492-A-G

148433147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644406-G-A

148433147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644406-G-T

148433155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644401-G-A

148433155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644401-G-T

148433163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644393-G-T

148433222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644362-A-G

148433223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644361-T-A

148433223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644361-T-G

148433248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62644333-G-A

148433519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62644088-G-A

148433540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644067-T-C

148433540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644067-T-G

148433578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62644033-A-G

http://identifiers.org/hco/5/GRCh38#148433607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62643910-A-C

148433822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643472-T-A

148433863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643441-T-C

http://identifiers.org/hco/5/GRCh38#148433899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62643403-C-A

148433899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643403-C-T

148433974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643348-T-C

148434016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643308-G-C

http://identifiers.org/hco/5/GRCh38#148434076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62643262-C-A

148434133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643213-A-T

148434179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643169-A-T

http://identifiers.org/hco/5/GRCh38#148434188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62643160-C-A

148434188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643160-C-T

148434196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643157-T-C

148434199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643154-T-C

148434199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62643154-T-G

http://identifiers.org/hco/5/GRCh38#148436698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62642313-A-C

148436703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62642308-A-G

148436931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62642126-A-G

148437036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62642050-G-A

148437543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641762-T-C

148437737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641615-A-G

http://identifiers.org/hco/5/GRCh38#148437872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62641532-C-A

148437872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641532-C-G

148438003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641408-C-G

148438059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641347-C-T

148438136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641268-T-C

148438161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641229-A-G

148438195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641205-A-T

148438207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641193-T-A

148438215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641186-G-A

148438215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641186-G-T

148438229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641171-T-C

148438244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62641156-T-C

148438529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640873-A-G

148438533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640869-A-G

148438560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640839-T-A

148438560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640839-T-C

148438777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640601-C-T

148438956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640449-A-G

http://identifiers.org/hco/5/GRCh38#148439071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62640348-C-A

148439071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640348-C-G

148439270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62640175-G-A

148439507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639944-T-C

148439542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639909-A-G

148439636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639829-G-A

148439806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639667-T-C

148439806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639667-T-G

148439808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639665-G-A

148439808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639665-G-T

148439818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639655-G-A

http://identifiers.org/hco/5/GRCh38#148439849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62639625-C-A

148439849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639625-C-G

148439849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639625-C-T

148439932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639582-G-A

148440029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639489-C-T

148440145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639375-A-G

148440250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639267-G-T

148440273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62639246-T-G

148440386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 62639146-T-C

148440459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62639075-C-T

148440600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638994-G-A

148440818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638944-G-A

148440847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638914-T-C

148440940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638824-A-G

148440963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638803-C-T

148440996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638776-G-T

148441004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62638767-T-G

http://identifiers.org/hco/5/GRCh38#148441015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62638756-C-A

148441207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62638574-G-A

148441207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 62638574-G-T

148441303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62638478-A-G

http://identifiers.org/hco/5/GRCh38#148441330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62638450-C-A

148441340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62638437-T-C

148441460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62638403-A-G

148441508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638356-T-C

148441548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638318-A-G

http://identifiers.org/hco/5/GRCh38#148441577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#62638294-C-A

148441586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638285-G-A

148441586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638285-G-T

148441756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638141-G-A

148441838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638054-C-T

148441840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638052-T-A

148441840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: intron variant
orthologous variants: 62638052-T-G

148442085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense variant
orthologous variants: 62637833-G-C

148442088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: missense variant
orthologous variants: 62637830-G-A

148442507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 3 prime UTR variant
orthologous variants: 62637442-A-G

148442607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 3 prime UTR variant
orthologous variants: 62637348-A-G

148442780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28844
most severe consequence: 3 prime UTR variant
orthologous variants: 62637186-A-G