150599629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60782718-A-G

150600100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60782381-C-T

150600719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781733-C-G

150600801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781652-G-A

150600801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781652-G-T

150601126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60781327-G-A

150601126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60781327-G-T

150601169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 60781285-G-T

150601326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781128-G-A

150601326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781128-G-T

150601416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781038-C-T

150601435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60781006-G-A

150601572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780900-T-C

150601573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780899-G-A

150601573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780899-G-T

http://identifiers.org/hco/5/GRCh38#150601638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60780845-A-C

150601638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780845-A-G

150602031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780540-T-A

150602031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780540-T-C

150602043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780528-G-A

150602043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780528-G-C

150602176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780391-C-T

150602246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780321-G-A

150602283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60780294-T-C

http://identifiers.org/hco/5/GRCh38#150602324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60780253-A-C

http://identifiers.org/hco/5/GRCh38#150602352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60780226-A-C

150602909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779732-C-G

http://identifiers.org/hco/5/GRCh38#150602947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60779704-C-A

150602947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779704-C-T

150602989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779662-C-T

150603021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779637-T-A

150603118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779575-G-A

150603203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779497-G-A

150603203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779497-G-T

150603460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779255-T-C

150603491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779227-G-A

150603491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779227-G-C

150603508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779212-A-G

150603536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779187-G-T

150603641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779085-G-A

150603655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60779071-G-C

150603778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778950-G-A

150603991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778821-T-A

150604240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778620-G-A

150604486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778410-G-A

150604549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778353-G-A

150604586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778316-G-A

150604670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778244-G-A

150604711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778205-A-T

150604842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778114-T-C

150604907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60778049-T-G

150605022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777956-A-G

150605032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777946-T-C

150605211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777792-G-C

150605360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777703-C-T

150605568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777524-C-T

150605585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777504-A-G

150605605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777484-G-A

150605649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777454-C-T

150605672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777435-G-A

150605683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777424-T-G

150605798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777348-T-A

150605813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777344-C-G

150605890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777275-C-T

150605996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777209-C-T

150606050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777167-C-T

150606200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777063-G-C

150606275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60777014-A-G

http://identifiers.org/hco/5/GRCh38#150606402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60776907-C-A

150606442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776867-A-G

150606596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776715-A-T

150606809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776513-G-A

150606817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776503-C-T

150606884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776438-T-C

http://identifiers.org/hco/5/GRCh38#150606931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60776431-A-C

150606931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776431-A-G

150607313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60776072-T-C

150607664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60773956-C-T

150607684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60773935-C-T

150607760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60773872-G-C

150607760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60773872-G-T

150608032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773603-C-T

150608067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773569-C-G

150608069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773567-C-T

150608073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773563-G-T

150608240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773413-A-G

150608240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773413-A-T

http://identifiers.org/hco/5/GRCh38#150608375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60773290-C-A

150608375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773290-C-T

150608393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773272-G-A

150608393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773272-G-T

http://identifiers.org/hco/5/GRCh38#150608491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60773178-C-A

150608491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60773178-C-G

150608602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60773074-G-A

150608630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60773047-A-G

http://identifiers.org/hco/5/GRCh38#150608663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60773014-C-A

150608663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60773014-C-T

150609111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60772618-T-C

150609111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60772618-T-G

150609904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60771535-T-C

150609916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60771523-A-T

150609983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60771478-C-T

150609984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60771477-C-T

http://identifiers.org/hco/5/GRCh38#150610349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60771161-C-A

150610489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60770869-C-G

150610489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60770869-C-T

150610993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60770299-T-C

150611235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60770048-A-G

150611498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60769813-C-T

150612049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60769331-C-T

150612282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60769142-G-A

http://identifiers.org/hco/5/GRCh38#150613106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60768473-C-A

150613140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768439-T-G

150614295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766850-A-G

150614525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766696-G-A

150614549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766674-A-G

150614747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766567-C-T

http://identifiers.org/hco/5/GRCh38#150614835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60766522-C-A

150614835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60766522-C-T

150614913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766434-T-C

http://identifiers.org/hco/5/GRCh38#150614949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60766401-C-A

150614949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766401-C-T

http://identifiers.org/hco/5/GRCh38#150614968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60766384-C-A

150614968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60766384-C-T

150615030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60766323-G-T

150615092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60766261-T-A

150615092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60766261-T-C

150615347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60766028-G-A

150615386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765989-G-A

http://identifiers.org/hco/5/GRCh38#150615421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60765956-C-A

150615421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765956-C-G

150615421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765956-C-T

http://identifiers.org/hco/5/GRCh38#150615497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60765886-C-A

150615497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765886-C-T

http://identifiers.org/hco/5/GRCh38#150615498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60765885-C-A

150615498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765885-C-T

150616027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60765432-C-T

150616142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 60765324-G-A

http://identifiers.org/hco/5/GRCh38#150616817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60764649-A-C

150617067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60764181-A-G

150617082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60764166-T-C

http://identifiers.org/hco/5/GRCh38#150617131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60764117-C-A

150617131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60764117-C-G

http://identifiers.org/hco/5/GRCh38#150618070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60763185-C-A

150618070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60763185-C-T

150618073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60763182-G-A

150618073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60763182-G-T

150618199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: 60763051-G-A

150618199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: 60763051-G-T

150618245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: 60763005-T-C

150618245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: 60763005-T-G

150618246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: 60763004-G-T

http://identifiers.org/hco/5/GRCh38#150618315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60762952-C-A

150618609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60762683-A-G

http://identifiers.org/hco/5/GRCh38#150618649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60762640-A-C

150618649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: synonymous variant
orthologous variants: 60762640-A-G

http://identifiers.org/hco/5/GRCh38#150618741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60762548-C-A

150618741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60762548-C-T

http://identifiers.org/hco/5/GRCh38#150618805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60762507-C-A

150619018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60762328-C-T

150619078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60762274-T-C

150619184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60762169-C-T

150619249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60762110-T-C

150619621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, undefined
orthologous variants: 60761776-G-A

150620037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60761397-A-G

150620538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60761000-A-G

150620571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60760978-T-C

150620622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60760940-G-A

150620622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60760940-G-T

150620828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60760776-C-T

150621414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60760610-A-T

150621583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60760443-G-A

150621760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60760288-C-G

150621760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60760288-C-T

150621909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60760156-G-C

150622088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60759983-G-C

150622832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60759095-C-T

150623637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60758334-G-A

150624403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60757710-G-A

150624536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60757594-C-T

150624559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60757569-C-T

150624585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60757539-G-A

150624585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60757539-G-T

150624713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60757412-C-T

150624867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60757281-G-A

150624867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60757281-G-C

150625272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60756890-A-T

150625360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60756826-G-A

150625782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60756425-A-G

150626369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60755980-G-A

150626453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60755944-A-G

150626586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60755823-G-A

150626677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60755721-G-A

150627553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60754453-G-A

150627709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60754305-C-T

150628465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60753655-T-A

150628465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60753655-T-C

150628560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60753567-G-A

150630576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60753026-A-G

150630788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60752801-C-T

150630825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60752764-C-T

150631230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60752352-C-G

150631230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60752352-C-T

150631460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60752140-G-A

150631646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751974-G-A

150631715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751933-A-G

150631751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751906-G-A

150632352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751546-G-A

150632606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751429-C-G

150632878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751152-T-C

150632878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751152-T-G

150632947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751024-C-T

150633276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750397-A-G

150633329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750353-A-G

150633559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750121-G-A

150633581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750102-G-A

150633763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749771-G-T

150634026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749499-A-G

150634188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749361-C-T

150634189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749360-C-T

150634193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749356-G-A

150634193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749356-G-T

150634268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749306-A-T

150634962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60749019-G-A

http://identifiers.org/hco/5/GRCh38#150635013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60748976-C-A

150635246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60748739-C-T

150635854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60748510-C-G

150636192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60748237-C-G

150636415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60748025-G-A

150636793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747582-G-A

150636793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747582-G-T

150636921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747412-G-A

150636923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747410-G-A

150636929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747404-C-T

150637134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747259-A-G

150637198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747214-G-A

150637214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747198-G-A

150637214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60747198-G-T

http://identifiers.org/hco/5/GRCh38#150637529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60746899-A-C

150637804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746624-T-C

150637806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746622-C-T

150637808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746620-C-T

150638061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746364-T-C

150638080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746352-T-G

150638252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746222-T-C

150638464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60746028-A-G

150639544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60744181-C-T

150639569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60744151-C-T

150639610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60744100-C-G

150640477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743357-G-A

150640543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743299-A-G

150640544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743298-T-G

150640616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743220-G-A

150640616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743220-G-T

150640637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743199-G-A

150640637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60743199-G-T

150640709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743125-C-T

150640750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743079-T-C

http://identifiers.org/hco/5/GRCh38#150640754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60743075-C-A

150640787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743042-A-G

150640812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743023-G-A

150640812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743023-G-T

150640815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 60743020-C-T

150640942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742896-T-C

150640948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742890-G-T

150640967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742871-T-C

http://identifiers.org/hco/5/GRCh38#150640978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60742860-C-A

150640978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742860-C-T

150640994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742847-G-A

150640994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742847-G-T

150641016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742827-G-A

150641530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742357-G-A

150641603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60742291-G-A

150642065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60741853-T-A

150642082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60741836-C-T

150642257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60741668-T-C

150642584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60741425-G-A

http://identifiers.org/hco/5/GRCh38#150642788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60741209-C-A

150642960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60741059-G-T

150643333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60740675-T-C

150644322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60740399-G-A

150644323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60740398-A-G

150644323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60740398-A-T

150644411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60740330-G-A

150644725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739989-G-C

150644744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739970-C-T

150644768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739946-C-T

http://identifiers.org/hco/5/GRCh38#150644934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60739799-A-C

150644977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739763-G-A

150645402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739378-C-T

150645488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739297-G-A

150645488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739297-G-C

150645864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739025-C-T

150646139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60738823-G-A

150646162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60738800-T-A

150646834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60738192-G-C

150646925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60738121-C-T

150647700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737725-A-G

150647885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737600-G-A

150647885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737600-G-T

150647921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737582-T-A

http://identifiers.org/hco/5/GRCh38#150648180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60737321-C-A

150648180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 60737321-C-G

150648180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 60737321-C-T

150648348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 60737153-C-T

http://identifiers.org/hco/5/GRCh38#150648542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60736959-C-A

150648543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60736958-A-G

150648564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60736937-A-G

150648668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60736857-T-C

150648818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60736704-G-A

150648818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60736704-G-T

150649026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60736499-A-G

150649107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60736418-C-T

http://identifiers.org/hco/5/GRCh38#150649192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60736333-C-A

150649230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60736295-C-T

150649290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60736235-T-G

http://identifiers.org/hco/5/GRCh38#150649434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60736091-C-A

150649434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60736091-C-G

150649506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60736019-C-G

150649587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735938-G-A

150649587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735938-G-T

150649857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735671-G-A

150649888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735640-G-A

150649888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735640-G-C

150649888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735640-G-T

http://identifiers.org/hco/5/GRCh38#150649890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60735638-A-C

150649911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60735617-C-T

150650577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734940-A-G

150650684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734835-G-T

150650688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734831-A-G

150650879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734667-G-A

150650879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734667-G-C

150650879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734667-G-T

150650939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734616-C-G

150650940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734615-C-T

150651006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734524-T-C

http://identifiers.org/hco/5/GRCh38#150651037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60734490-C-A

150651039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734488-G-A

150651128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734399-G-T

150651167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734361-G-T

150651210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734330-A-G

150651222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734324-G-T

150651239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734307-G-A

150651239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734307-G-T

http://identifiers.org/hco/5/GRCh38#150651247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60734299-C-A

150651247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734299-C-T

150651258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734288-G-A

http://identifiers.org/hco/5/GRCh38#150651279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60734267-C-A

150651279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734267-C-T

150651519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734035-A-G

http://identifiers.org/hco/5/GRCh38#150651525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60734029-C-A

150651525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734029-C-T

150651543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734012-G-A

150651543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734012-G-T

150651547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734008-G-A

150651547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734008-G-C

150651547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60734008-G-T

150651585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733968-G-A

150651585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733968-G-T

150652023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733587-G-A

150652030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733580-T-G

150652031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733579-G-A

150652031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733579-G-T

http://identifiers.org/hco/5/GRCh38#150652059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60733557-C-A

150652059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733557-C-G

150652150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733461-A-G

http://identifiers.org/hco/5/GRCh38#150652152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60733459-C-A

150652152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733459-C-G

150652152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733459-C-T

150652161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733450-T-C

150652161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733450-T-G

150652241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733369-G-A

150652241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733369-G-T

150652272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733338-G-T

http://identifiers.org/hco/5/GRCh38#150652311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60733305-C-A

150652311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733305-C-G

http://identifiers.org/hco/5/GRCh38#150652429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60733187-C-A

150652460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733151-T-C

150652492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60733120-G-T

http://identifiers.org/hco/5/GRCh38#150652714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60732275-C-A

150652736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732253-G-T

http://identifiers.org/hco/5/GRCh38#150652740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60732249-C-A

150652740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732249-C-T

150652774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732214-T-C

150652774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732214-T-G

150652775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732213-T-C

http://identifiers.org/hco/5/GRCh38#150652787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60732204-C-A

150652807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732184-T-A

150652917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732158-G-T

150652920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732155-A-G

150653052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732022-G-A

150653056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732018-C-T

150653065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60732009-G-T

150653081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731996-G-A

150653081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731996-G-T

150653083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731994-G-T

150653144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731934-G-A

150653144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731934-G-T

150653196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731883-C-T

150653211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731870-C-G

150653217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731864-T-C

150653239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731844-A-G

http://identifiers.org/hco/5/GRCh38#150653280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60731804-C-A

150653324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731792-T-C

150653326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731790-A-G

http://identifiers.org/hco/5/GRCh38#150653732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60731267-C-A

150653732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731267-C-T

150653809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731139-T-C

150653869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731094-G-A

150653885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731080-T-C

150653926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731040-T-C

150653944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731023-G-A

150653944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60731023-G-T

150653980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60730993-T-C

http://identifiers.org/hco/5/GRCh38#150654000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60730973-C-A

http://identifiers.org/hco/5/GRCh38#150654004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60730969-C-A

150654026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60730944-G-T

150654033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60730937-A-G

150654063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60730910-G-T

http://identifiers.org/hco/5/GRCh38#150654148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60730839-C-A

150654148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 60730839-C-T

150654259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60730733-T-A

150654259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60730733-T-C

150654271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60730721-G-T

http://identifiers.org/hco/5/GRCh38#150654322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60730652-C-A

150654404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60730580-A-T

150654426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60730558-T-C

http://identifiers.org/hco/5/GRCh38#150656394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729568-C-A

150656394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60729568-C-G

150656394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: intron variant
orthologous variants: 60729568-C-T

http://identifiers.org/hco/5/GRCh38#150656458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729504-C-A

150656458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729504-C-T

http://identifiers.org/hco/5/GRCh38#150656503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729459-C-A

150656503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729459-C-T

150656506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729456-G-C

150656506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729456-G-T

http://identifiers.org/hco/5/GRCh38#150656578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729384-C-A

150656578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729384-C-T

150656584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729378-G-A

150656584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729378-G-C

150656584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729378-G-T

http://identifiers.org/hco/5/GRCh38#150656740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729222-C-A

150656740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729222-C-G

150656740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729222-C-T

150656755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729207-C-G

150656755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729207-C-T

150656777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729203-G-A

150656777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729203-G-C

150656777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729203-G-T

http://identifiers.org/hco/5/GRCh38#150656800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60729180-C-A

150656800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60729180-C-T

150656944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729039-G-A

150656944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense_variant, undefined
orthologous variants: 60729039-G-T

150656965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60729018-T-A

150656965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60729018-T-C

150656971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60729012-G-T

150657031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: missense variant
orthologous variants: 60728952-G-T

http://identifiers.org/hco/5/GRCh38#150657107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60728882-C-A

150657107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728882-C-G

150657107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728882-C-T

http://identifiers.org/hco/5/GRCh38#150657110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60728879-C-A

150657110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728879-C-T

150657232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728746-G-A

150657232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728746-G-T

150657307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728671-A-T

150657490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728608-T-C

150657550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728552-C-T

150657574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728534-C-T

150657577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728531-T-C

150657582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728526-A-G

150657582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728526-A-T

150657695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728415-C-T

150657702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728408-T-G

150657747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728364-T-C

150657796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728314-A-G

http://identifiers.org/hco/5/GRCh38#150657948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60728165-C-A

150657948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60728165-C-T

150658261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727911-G-A

150658261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727911-G-T

http://identifiers.org/hco/5/GRCh38#150658561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727686-C-A

150658561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727686-C-G

150658561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727686-C-T

150658685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727549-T-C

150658706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727509-G-A

150658706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727509-G-T

150658723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727499-A-G

150658745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 60727477-A-G

150658828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727382-G-A

150658828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727382-G-T

http://identifiers.org/hco/5/GRCh38#150658931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727319-C-A

150658931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727319-C-T

http://identifiers.org/hco/5/GRCh38#150658972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727278-C-A

150658972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727278-C-T

http://identifiers.org/hco/5/GRCh38#150658992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727258-C-A

150658992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727258-C-T

http://identifiers.org/hco/5/GRCh38#150659026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727223-C-A

150659066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727183-T-C

http://identifiers.org/hco/5/GRCh38#150659090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#60727176-C-A

150659129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30672
most severe consequence: 3 prime UTR variant
orthologous variants: 60727128-C-T