158893411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371545-T-C

158893411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371545-T-G

http://identifiers.org/hco/4/GRCh38#158893530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371438-C-A

158893530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79371438-C-T

158893555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79371416-G-T

http://identifiers.org/hco/4/GRCh38#158893666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371334-C-A

158893666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79371334-C-T

158893764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371248-G-A

158893764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371248-G-T

http://identifiers.org/hco/4/GRCh38#158893800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371213-A-C

158893800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371213-A-G

http://identifiers.org/hco/4/GRCh38#158893806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79371207-C-A

158893806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371207-C-T

158893848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371168-T-A

158893852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79371164-G-A

158894195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370911-G-T

158894353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370852-G-A

158894617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370794-A-G

158894675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370738-A-G

158894714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370695-T-A

158894763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370644-T-C

158894833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370588-G-T

158895032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370392-G-A

158895049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370375-G-A

158895090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370334-A-G

158895124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370301-A-G

158895185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370244-A-G

158895414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370024-A-G

158895424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79370013-T-C

158895527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369816-A-T

158895546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369780-G-A

158895626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-A

158895626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-C

158895626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369670-G-T

158895640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369656-G-A

158895640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369656-G-T

158895727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369572-T-C

158895731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369568-A-G

http://identifiers.org/hco/4/GRCh38#158895915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369380-C-A

158895915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369380-C-T

http://identifiers.org/hco/4/GRCh38#158895955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369331-C-A

158895955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369331-C-G

158895955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369331-C-T

http://identifiers.org/hco/4/GRCh38#158895964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369320-C-A

158895964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79369320-C-T

http://identifiers.org/hco/4/GRCh38#158896014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79369275-C-A

http://identifiers.org/hco/4/GRCh38#158896585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79368889-A-C

158896612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79368853-T-C

158903804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367777-C-G

158903804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367777-C-T

158903843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367740-C-T

http://identifiers.org/hco/4/GRCh38#158904242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79367403-C-A

158904242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367403-C-G

158904376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-A

158904376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-C

158904376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79367112-G-T

158904544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79366968-A-G

158904610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366924-A-G

158904611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366923-T-A

158904613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366921-A-G

http://identifiers.org/hco/4/GRCh38#158904757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366784-C-A

http://identifiers.org/hco/4/GRCh38#158904876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366676-A-C

158904894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-A

158904894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-C

158904894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366657-G-T

158905008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366573-C-T

http://identifiers.org/hco/4/GRCh38#158905105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79366481-C-A

158905105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366481-C-T

158905193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366392-T-C

158905280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366332-G-A

158905322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366299-T-C

158905365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366260-G-A

158905365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366260-G-T

158905457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366167-A-G

158905537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79366102-A-G

158905676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365962-G-A

http://identifiers.org/hco/4/GRCh38#158905711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365950-C-A

158905749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365913-T-C

158905797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365870-G-A

158905797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365870-G-C

158905866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365810-A-G

http://identifiers.org/hco/4/GRCh38#158905924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365760-A-C

158905966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365698-T-C

158906014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365655-T-C

158906096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365516-G-A

158906096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365516-G-T

http://identifiers.org/hco/4/GRCh38#158906186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365429-A-C

158906293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365373-A-G

158906295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365371-A-G

158906307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365355-A-G

158906399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365275-G-T

158906439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79365235-C-T

158906499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79365181-A-G

http://identifiers.org/hco/4/GRCh38#158906596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79365085-C-A

http://identifiers.org/hco/4/GRCh38#158906796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79364936-A-C

158906845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364891-G-A

http://identifiers.org/hco/4/GRCh38#158906921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79364838-C-A

158907032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364732-T-A

158907040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364724-G-A

158907130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364634-T-A

158907550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79364232-G-T

http://identifiers.org/hco/4/GRCh38#158907851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79363945-A-C

158907853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79363943-G-A

158907922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79363863-T-C

158908116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79363493-T-C

158908254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79363380-G-A

158908352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79363303-C-T

158908600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79363095-A-G

158908657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79363040-C-T

158910620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79362210-G-A

158910698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79362158-T-C

158910736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79362128-T-A

158910816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79362053-C-T

158910846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79362023-A-G

158910933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79361968-A-T

158910950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79361951-A-G

158910987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79361919-G-A

158911212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360654-C-G

158911212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360654-C-T

158911288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360584-C-T

158911456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360397-A-T

158911484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360369-A-G

158911535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360323-T-C

158911555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360314-C-T

158911647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79360221-C-T

158911828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79359999-C-T

158912529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79359299-T-G

158912570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79359259-T-A

158912570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79359259-T-G

158912654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79359180-T-C

158913879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358654-G-A

158913983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358521-T-C

158914021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358490-A-G

158914057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358433-T-G

158914064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358426-T-A

158914095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358391-T-A

http://identifiers.org/hco/4/GRCh38#158914191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79358319-C-A

158914197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358313-C-G

158914219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358291-G-A

http://identifiers.org/hco/4/GRCh38#158914239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79358266-C-A

158914279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358226-A-G

158914283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358222-G-A

158914472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79358004-T-C

158914481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79357998-G-A

158914533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79357944-C-T

158914793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79357081-A-G

158914892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356985-C-G

158914897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356981-A-G

158914910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356968-C-T

http://identifiers.org/hco/4/GRCh38#158915048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79356830-C-A

158915048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356830-C-T

158915085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356797-A-T

158915098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356784-A-G

158915141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356757-T-C

http://identifiers.org/hco/4/GRCh38#158915347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79356562-A-C

158915430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356450-G-T

158915432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356448-G-A

158915432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356448-G-C

158915432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356448-G-T

158915475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356406-T-A

158915571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356299-C-G

158915673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79356199-C-T

158935590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79353220-C-T

158935759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79353020-T-G

158936716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79352150-T-G

158936980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351898-C-T

158937038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351855-G-C

158937049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351844-T-A

158937049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351844-T-C

158937294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351583-A-G

158937443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351016-A-G

158937639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350686-T-C

158937698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350619-A-G

158938388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79348967-C-G

158938409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79348947-G-A

158939213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79348272-A-G

http://identifiers.org/hco/4/GRCh38#158941150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79344305-C-A

158941150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79344305-C-T

158941937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343744-A-T

158942052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343630-A-G

158942292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343392-C-T

158942854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343203-T-G

158942984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343079-A-T

158942995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343068-G-A

158942995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79343068-G-T

158943205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79342904-G-T

158943367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79342745-T-C

158943452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79342583-T-C

158943467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79342568-T-G

158945976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79340372-G-A

158946006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79340351-A-T

158946046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79340309-T-C

158946088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79340271-C-T

158946251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79340109-T-C

158947148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79336775-A-G

http://identifiers.org/hco/4/GRCh38#158947267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79336656-C-A

158947357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79336571-A-G

158947438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79336493-T-C

158951019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333747-G-C

158951613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333524-T-C

158951618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333517-G-A

158951980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333283-G-C

158952141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333153-T-C

158954505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79333017-C-T

158954747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331731-G-A

158954750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331728-A-G

http://identifiers.org/hco/4/GRCh38#158954867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79331638-C-A

158954982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331526-C-T

158955305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79331278-T-C

http://identifiers.org/hco/4/GRCh38#158955356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79331237-C-A

158955985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330939-A-G

158956028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330897-G-A

158956067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330859-C-T

158956121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330796-T-C

158956256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330656-T-C

158957243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79330067-T-A

158959102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79328012-T-C

158959141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327974-T-G

158959265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327850-T-C

158959524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327430-T-C

158959692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327309-G-T

http://identifiers.org/hco/4/GRCh38#158959722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79327282-A-C

158959722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327282-A-G

158959759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327246-T-G

158959901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79327104-C-G

158960087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326931-T-C

http://identifiers.org/hco/4/GRCh38#158960150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79326870-A-C

158960160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326855-T-C

158960160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326855-T-G

158960196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326813-A-G

158960196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326813-A-T

158960209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326798-G-A

158960209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326798-G-T

158960275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326735-T-C

http://identifiers.org/hco/4/GRCh38#158960318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79326692-A-C

158960318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79326692-A-G

158960373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326635-T-A

158960373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326635-T-G

http://identifiers.org/hco/4/GRCh38#158960403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79326595-A-C

158960403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326595-A-G

http://identifiers.org/hco/4/GRCh38#158960468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79326532-A-C

158960468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326532-A-G

158960468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326532-A-T

158960556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326448-T-G

158960900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326125-T-A

158960900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326125-T-C

http://identifiers.org/hco/4/GRCh38#158960910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79326111-A-C

158960930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79326091-C-T

158961326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325747-T-C

http://identifiers.org/hco/4/GRCh38#158961380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79325709-C-A

158961436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325655-A-G

http://identifiers.org/hco/4/GRCh38#158961495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79325593-C-A

158961597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325515-A-T

158961842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325283-T-G

158961930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325209-G-A

158961973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79325087-T-C

158962193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324844-A-G

158962605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324438-A-G

158962621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324422-G-A

158962621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324422-G-T

158962707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324336-G-C

158962861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324185-T-A

158962861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79324185-T-G

158965280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79320714-T-G

http://identifiers.org/hco/4/GRCh38#158965370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79320623-A-C

158966527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318855-C-T

158966551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318838-A-G

158966739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318678-T-C

158966767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318648-C-G

158966767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318648-C-T

158966808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318607-T-C

158967023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79318285-G-A

158967397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79317728-A-T

158967540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79317320-A-G

158967595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79317264-T-C

158967753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79317076-G-A

158967787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79317042-A-G

158967993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316841-G-A

http://identifiers.org/hco/4/GRCh38#158968382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79316766-A-C

158968525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316642-A-G

158968527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316640-T-C

158968675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316536-C-G

158968770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316443-A-G

158968803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316406-T-C

158969068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316173-G-A

158969080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79316161-T-C

http://identifiers.org/hco/4/GRCh38#158969216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79316024-A-C

158969268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315973-C-T

158969466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315779-T-C

158969584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315588-A-G

158969768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315382-C-T

158969777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315380-G-A

158969807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315350-T-C

158969838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79315323-A-T

http://identifiers.org/hco/4/GRCh38#158969869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79315293-C-A

158972496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313956-T-C

158972916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313387-G-A

158972916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313387-G-C

158972985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313313-A-G

158972985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313313-A-T

http://identifiers.org/hco/4/GRCh38#158973010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79313289-A-C

158973010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313289-A-G

158973010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313289-A-T

158973047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313252-T-A

158973047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313252-T-C

158973048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79313251-A-T

158973072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79313226-G-A

158973072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79313226-G-T

158973554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79312684-T-C

158973692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79312537-C-T

158974059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79312478-T-C

http://identifiers.org/hco/4/GRCh38#158974195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79312327-C-A

158994431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79305795-G-A

158999481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79296258-A-G

158999527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79296210-C-T

158999530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79296207-T-C

159002200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79296091-T-A

159002347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295949-T-A

159002347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295949-T-C

http://identifiers.org/hco/4/GRCh38#159002392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79295905-A-C

159002533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295628-C-T

159002638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295493-T-A

159002638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295493-T-C

159002815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79295350-C-G

http://identifiers.org/hco/4/GRCh38#159003349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79294812-A-C

159003881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79294552-G-A

159004700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79294334-G-A

159005539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79293751-G-A

159005634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79293672-C-T

159005689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79293622-T-G

159006177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79293193-A-G

159006393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79292978-A-G

159006397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79292974-T-G

159006398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79292973-G-A

159006407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79292964-C-T

http://identifiers.org/hco/4/GRCh38#159006429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79292942-C-A

159006432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79292939-C-T

159006575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79292794-A-G

http://identifiers.org/hco/4/GRCh38#159006691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79292680-A-C

159009300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79290622-C-T

http://identifiers.org/hco/4/GRCh38#159009634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79288823-C-A

159010740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287782-G-A

159011006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287532-A-G

159011067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287470-G-A

159011074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287463-T-A

159011270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287287-T-G

159011285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287272-C-T

159011328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287235-A-T

159011443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79287129-T-G

159015399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79278452-T-C

159015586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79278284-T-G

159020536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79275040-C-T

159020562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79275028-A-G

159021043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79274633-G-A

159021241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79274556-C-T

159021605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79274216-C-T

159021976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79273834-G-T

159024551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79270903-A-G

159024647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79270818-T-C

159024885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79270628-C-T

159025796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79269739-T-A

159025956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79269616-A-G

159027138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79268792-G-A

159027350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79268488-A-T

159027568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79268263-T-C

159027896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79267935-T-A

159028051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79267774-T-C

159028154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79267681-G-A

159033755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79253667-T-C

http://identifiers.org/hco/4/GRCh38#159034364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79253103-A-C

159034364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79253103-A-T

http://identifiers.org/hco/4/GRCh38#159034439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79253032-C-A

159035135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252746-G-A

159035135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252746-G-T

http://identifiers.org/hco/4/GRCh38#159035167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79252716-A-C

159035171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252712-C-T

159035213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252673-A-G

159035250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252636-T-C

http://identifiers.org/hco/4/GRCh38#159035289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79252598-C-A

159035289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79252598-C-T

159036631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79252253-T-A

159036753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79252135-G-A

159036875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26342
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79252038-G-A