167809411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403582-T-C

http://identifiers.org/hco/1/GRCh38#167809427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165403566-C-A

167809427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403566-C-G

167809458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403536-G-A

167809458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403536-G-T

http://identifiers.org/hco/1/GRCh38#167809465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165403529-A-C

167809465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403529-A-T

167809477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403517-T-C

167809533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403477-A-G

167809562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403448-G-A

167809562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403448-G-T

167809568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403442-G-T

167809595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403417-G-T

167809605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3 prime UTR variant
orthologous variants: 165403408-A-G

167809659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 165403354-A-G

167809864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165403146-G-A

http://identifiers.org/hco/1/GRCh38#167810483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165400544-A-C

167810616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400416-A-T

167810621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400411-T-C

167810669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400368-G-T

167810679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400358-T-A

167810683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400335-G-C

167810683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400335-G-T

167810694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400324-C-T

167810708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165400275-T-A

167810762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 165400221-C-T

167818016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165398436-A-T

167818023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165398429-G-A

167818023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165398429-G-T

167818094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165398359-G-C

167818094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165398359-G-T

167818172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165398281-T-A

167818211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165398242-T-C

167818272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 165398181-A-G

http://identifiers.org/hco/1/GRCh38#167818297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165398156-C-A

http://identifiers.org/hco/1/GRCh38#167818444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165398038-C-A

167818469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165398016-G-A

167820432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397197-T-G

167820448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397182-A-G

167820448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397182-A-T

http://identifiers.org/hco/1/GRCh38#167820477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165397153-A-C

167820495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397135-G-T

167820510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397120-T-A

167820612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397018-A-G

167820619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397011-T-C

167820623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397007-T-C

http://identifiers.org/hco/1/GRCh38#167820624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165397006-C-A

http://identifiers.org/hco/1/GRCh38#167820627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#165397003-C-A

167820627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165397003-C-T

167821543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165396081-G-A

167821563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165396062-G-C

167821819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165395521-T-C

http://identifiers.org/hco/1/GRCh38#167821873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395473-C-A

167821873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395473-C-T

167821905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395441-C-T

http://identifiers.org/hco/1/GRCh38#167821919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395427-C-A

167821934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395412-T-C

167821959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395376-A-G

167821960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395375-G-A

167821960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395375-G-C

167821960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395375-G-T

http://identifiers.org/hco/1/GRCh38#167821963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395372-C-A

167822003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395332-T-G

http://identifiers.org/hco/1/GRCh38#167822012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395323-A-C

167822090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165395245-T-C

167822129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165395206-C-T

167822135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165395200-A-G

167822229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395099-G-T

http://identifiers.org/hco/1/GRCh38#167822271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395053-C-A

167822271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395053-C-G

167822271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395053-C-T

http://identifiers.org/hco/1/GRCh38#167822272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165395052-C-A

167822272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165395052-C-T

167822731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165393379-A-G

167822811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165393312-T-C

http://identifiers.org/hco/1/GRCh38#167822999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165392957-C-A

http://identifiers.org/hco/1/GRCh38#167823001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165392955-C-A

167823001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 165392955-C-G

167823002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165392954-A-G

167823643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165392792-T-C

http://identifiers.org/hco/1/GRCh38#167823832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165392598-C-A

167824400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391967-G-A

167824400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391967-G-T

http://identifiers.org/hco/1/GRCh38#167824443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165391901-C-A

167824443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391901-C-T

167824460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391884-G-A

167824460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391884-G-T

167824633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391712-T-C

167824639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391706-G-T

167824776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165391569-A-G

167824987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391379-G-A

167824987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391379-G-T

167825058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391308-C-G

167825069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165391297-T-A

http://identifiers.org/hco/1/GRCh38#167825174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165391191-A-C

167825374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 165390991-G-A

167826033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165390743-G-A

167826134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165390684-A-G

167826389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165390443-C-T

http://identifiers.org/hco/1/GRCh38#167826400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165390433-A-C

167829220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165389451-C-T

167829248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165389424-A-G

http://identifiers.org/hco/1/GRCh38#167829358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, stop_lost
orthologous variants: http://identifiers.org/mco/1/GRCm39#165389307-C-A

167829478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165389197-T-C

167832384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165387408-T-A

167832705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165387125-G-A

http://identifiers.org/hco/1/GRCh38#167832838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165387027-C-A

167832838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165387027-C-T

http://identifiers.org/hco/1/GRCh38#167832848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165387013-C-A

167832848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165387013-C-T

167832919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386942-T-C

167832950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386906-G-A

167832950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386906-G-C

167832950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386906-G-T

167833023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 165386833-T-C

167833067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 165386789-G-A

167833068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 165386788-G-C

167833089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165386767-A-T

167833095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 165386761-T-A

167833095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 165386761-T-C

167833248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386619-G-A

167833248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386619-G-T

167833769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386372-A-T

http://identifiers.org/hco/1/GRCh38#167833772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165386369-C-A

167833878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386317-G-A

167833878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165386317-G-T

167834104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 165386090-G-T

http://identifiers.org/hco/1/GRCh38#167834139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165386064-C-A

167834139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 165386064-C-T

167834140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 165386063-C-T

167834142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 165386061-T-C

http://identifiers.org/hco/1/GRCh38#167834212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165386000-C-A

http://identifiers.org/hco/1/GRCh38#167834297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165385917-A-C

167836206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384662-T-A

167836206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384662-T-C

167836234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384634-G-A

167836234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384634-G-T

http://identifiers.org/hco/1/GRCh38#167836274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165384601-C-A

167836274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384601-C-G

167836274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384601-C-T

167836469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 165384387-T-A

167836469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 165384387-T-C

167836469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 165384387-T-G

167836478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 165384378-G-A

167836534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 165384322-T-C

167836905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384038-G-A

167836905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165384038-G-T

http://identifiers.org/hco/1/GRCh38#167837378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165383769-C-A

http://identifiers.org/hco/1/GRCh38#167837394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165383753-A-C

167837394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165383753-A-G

167837765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165383378-T-G

http://identifiers.org/hco/1/GRCh38#167845393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165379899-C-A

167845397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379896-T-A

167845397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379896-T-C

http://identifiers.org/hco/1/GRCh38#167845410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165379883-C-A

167845410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379883-C-T

167845445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379861-T-A

167845445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379861-T-C

167845577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165379730-G-C

167845775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165379532-A-T

167845830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165379477-G-A

167845887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379420-A-G

167845903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165379404-G-T

167846035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165378876-G-A

167846035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 165378876-G-T

167846179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165378732-G-A

167846194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165378717-A-G

167846194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165378717-A-T

167846391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165378529-A-G

167846392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165378528-A-G

167846392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165378528-A-T

167846488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165378473-A-T

167846517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 165378445-T-G

167848393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165375776-A-T

167848429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165375740-C-T

167848450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165375722-G-A

167848450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165375722-G-C

167848450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 165375722-G-T

167848529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375646-C-T

167848530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375645-C-T

167848561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375613-T-G

http://identifiers.org/hco/1/GRCh38#167848611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165375565-C-A

167848611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375565-C-T

http://identifiers.org/hco/1/GRCh38#167848615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165375561-A-C

167848626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375550-A-T

167849058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165375441-C-T

http://identifiers.org/hco/1/GRCh38#167849288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165375298-A-C

167854248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374316-C-T

167854466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense variant
orthologous variants: 165374108-C-T

167854526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374049-A-G

167854530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374045-A-G

167854541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374034-A-G

167854542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374033-G-A

167854582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165374004-T-G

167855560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371531-C-T

167855593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371498-T-C

167855648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371463-C-T

167855649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371462-G-A

167855649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371462-G-C

167855666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371446-T-C

http://identifiers.org/hco/1/GRCh38#167855687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165371423-A-C

167855759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371351-C-T

167855836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371252-A-G

167855915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371178-A-T

167855967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371140-C-T

167856014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371095-G-A

167856046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371029-G-A

167856046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371029-G-T

167856049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371026-G-A

167856049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371026-G-T

167856066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165371006-A-G

167856080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165370983-G-T

167856482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165370585-T-A

167856542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165370486-T-A

167856909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165370167-G-A

167859681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369350-A-T

http://identifiers.org/hco/1/GRCh38#167859695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165369337-A-C

167859695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369337-A-G

167859695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369337-A-T

167859808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 165369226-A-G

167859809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 165369225-G-A

167859809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 165369225-G-C

167859897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165369137-T-A

167859908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369129-A-G

167859926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369111-G-A

167859926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369111-G-T

167859964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369085-G-A

167859981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165369067-T-G

http://identifiers.org/hco/1/GRCh38#167860000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165369048-C-A

167860788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165367614-G-T

167860917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: stop gained
orthologous variants: 165367495-A-T

167860926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense variant
orthologous variants: 165367486-A-G

167860926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense variant
orthologous variants: 165367486-A-T

167860989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense variant
orthologous variants: 165367423-A-G

167861016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: missense variant
orthologous variants: 165367396-T-C

167862967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366622-T-C

http://identifiers.org/hco/1/GRCh38#167862981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165366609-A-C

167862983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366607-C-T

http://identifiers.org/hco/1/GRCh38#167863024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165366565-A-C

167863087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366502-C-G

167869975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, undefined
orthologous variants: 165366402-C-T

167870106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, undefined
orthologous variants: 165366269-T-C

167870127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366247-A-G

167870170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366203-A-G

167870170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366203-A-T

167870183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366190-T-C

167870203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366173-A-G

167870226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165366131-T-C

http://identifiers.org/hco/1/GRCh38#167870478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165365871-C-A

http://identifiers.org/hco/1/GRCh38#167870493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165365856-C-A

167870522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165365822-G-A

167870522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165365822-G-T

167870549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165365802-T-C

167870862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165365534-A-T

167871690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165364812-T-C

167871795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165364704-C-G

167871859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165364640-C-T

167872651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165364198-G-A

167873179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363993-A-G

167873325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363865-G-A

167873372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363816-G-A

167873465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363542-G-A

167873465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363542-G-C

167873682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363341-A-G

167873693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165363330-A-G

http://identifiers.org/hco/1/GRCh38#167875278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165352493-C-A

167875278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165352493-C-T

167875295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165352476-A-G

167875570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165352226-T-C

167876329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351913-A-G

167876646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351652-A-G

http://identifiers.org/hco/1/GRCh38#167876661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165351637-A-C

167876676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351622-G-A

167876790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351518-T-G

167876858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351456-T-C

167876902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351412-A-G

167876957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351334-T-C

167876989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165351300-A-G

167877244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350979-G-A

167877255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350968-A-G

167877446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350779-T-C

http://identifiers.org/hco/1/GRCh38#167877496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165350733-C-A

167877545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350669-T-A

http://identifiers.org/hco/1/GRCh38#167877559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165350655-C-A

167877713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350493-G-A

167877773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350404-T-C

167877778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165350398-G-A

http://identifiers.org/hco/1/GRCh38#167877835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165350360-A-C

167878387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349604-A-G

167878387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349604-A-T

167878391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349591-T-C

http://identifiers.org/hco/1/GRCh38#167878664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165349316-C-A

167878664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349316-C-T

167878671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349300-A-G

167878745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349237-G-A

167878746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349236-T-C

http://identifiers.org/hco/1/GRCh38#167878759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165349223-C-A

167878784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349206-T-C

167878879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165349110-G-A

167879042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165348958-A-G

167879051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165348954-T-C

167880010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347611-G-T

http://identifiers.org/hco/1/GRCh38#167880047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165347551-C-A

167880047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347551-C-T

167880215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347413-G-A

167880215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347413-G-T

167880240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347368-G-A

167880240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347368-G-T

167880243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347365-T-A

167880243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347365-T-C

167880323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347285-T-A

http://identifiers.org/hco/1/GRCh38#167880338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165347270-C-A

167880338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347270-C-T

http://identifiers.org/hco/1/GRCh38#167880343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165347265-C-A

167880343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347265-C-T

167880408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347206-T-A

167880436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347178-A-G

167880436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165347178-A-T

167880500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165347112-T-C

167880614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165346998-G-C

167880614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165346998-G-T

167880717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165346915-G-C

167880717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165346915-G-T

167883358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165346056-T-C

167883370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165346036-A-G

167883403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165346004-A-G

167883417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345990-A-G

167883417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345990-A-T

167883427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345980-T-A

167883427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345980-T-C

167883428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345979-C-T

167883880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165345454-C-T

167891892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165344858-G-C

167893752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165343053-T-A

167893752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165343053-T-G

167893803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165343011-G-A

167893803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165343011-G-C

167893803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165343011-G-T

167893821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165342993-C-T

167893914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165342900-T-C

167894031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165342832-G-A

167894031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165342832-G-T

167894040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165342824-G-A

167894040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165342824-G-T

167896459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340871-G-A

167896459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340871-G-T

167896493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340837-T-G

167896495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340835-T-A

167896495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340835-T-G

http://identifiers.org/hco/1/GRCh38#167896503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165340827-C-A

167896503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340827-C-T

http://identifiers.org/hco/1/GRCh38#167896530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165340800-C-A

167896703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340626-C-T

167896757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340575-T-C

167896757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340575-T-G

167896778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340554-G-A

167896778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165340554-G-T

167896880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165339584-T-A

167899191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165338178-A-G

167899589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165337861-T-C

167899795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165337665-G-T

167901499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165334540-G-A

http://identifiers.org/hco/1/GRCh38#167901511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165334528-A-C

167901586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165334402-T-C

167901595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165334358-A-T

167901596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165334357-G-T

167901637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165334302-G-A

167901733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165334211-C-T

167901745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165334199-A-G

167901844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 165334101-T-A

167901844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 165334101-T-C

167901965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165333990-G-A

167902110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165333841-A-G

167904002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165331504-T-C

167904445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165331389-G-A

167904454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165331380-G-A

http://identifiers.org/hco/1/GRCh38#167904575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165331277-C-A

167904575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165331277-C-T

167904631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 165331224-A-G

167904631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 165331224-A-T

167904865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 165331013-A-G

167904962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, missense_variant
orthologous variants: 165330915-C-G

167904962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron_variant, stop_gained
orthologous variants: 165330915-C-T

167905180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165330697-C-T

167905249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165330624-T-C

167905251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165330622-C-T

167905510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165330229-C-G

http://identifiers.org/hco/1/GRCh38#167905579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165330170-C-A

167905579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165330170-C-T

167905631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165330123-T-C

167905996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165326627-T-C

167906033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165326608-G-T

167911969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165314077-A-G

http://identifiers.org/hco/1/GRCh38#167912022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165314022-A-C

167913282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165313508-T-C

167913566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165313236-T-C

167913571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165313231-C-T

http://identifiers.org/hco/1/GRCh38#167913918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#165312957-C-A

167913918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165312957-C-G

167913918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: intron variant
orthologous variants: 165312957-C-T

167914004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21285
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 165312876-C-T