http://identifiers.org/hco/5/GRCh38#139647428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35961917-C-A

139647527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35962025-G-A

139647527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35962025-G-T

139647779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35962263-A-G

139648212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35962701-G-A

139648267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35962751-G-A

139648267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35962751-G-T

http://identifiers.org/hco/5/GRCh38#139648513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35962962-C-A

139648515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35962964-T-C

139648533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35962982-T-C

139648533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35962982-T-G

http://identifiers.org/hco/5/GRCh38#139648542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35962991-C-A

139648542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35962991-C-T

http://identifiers.org/hco/5/GRCh38#139648907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35963350-C-A

139648907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35963350-C-T

139649202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35963637-G-T

http://identifiers.org/hco/5/GRCh38#139649349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35963765-C-A

139649349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35963765-C-T

http://identifiers.org/hco/5/GRCh38#139649423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35963839-C-A

139649463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35963879-C-T

139649475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35963891-G-A

139649475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35963891-G-T

139649504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35963920-C-T

http://identifiers.org/hco/5/GRCh38#139649612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35964047-A-C

139649734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964162-T-C

139649750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964181-G-T

http://identifiers.org/hco/5/GRCh38#139649797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35964228-C-A

139649797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964228-C-T

http://identifiers.org/hco/5/GRCh38#139649870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35964295-C-A

139649870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964295-C-T

139649930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964355-C-T

http://identifiers.org/hco/5/GRCh38#139650496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35964924-C-A

139650496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964924-C-T

139650497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964925-G-A

139650497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964925-G-C

139650569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964997-T-A

139650569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35964997-T-G

139650861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35965257-A-G

139650873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35965268-T-G

139650900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35965305-T-C

139650901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35965306-G-T

http://identifiers.org/hco/5/GRCh38#139650926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965331-C-A

139651005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965414-A-T

139651010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965419-T-C

http://identifiers.org/hco/5/GRCh38#139651053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965462-C-A

139651053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965462-C-T

http://identifiers.org/hco/5/GRCh38#139651056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965465-C-A

139651056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965465-C-G

139651056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965465-C-T

http://identifiers.org/hco/5/GRCh38#139651072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965481-C-A

139651072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965481-C-G

139651072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965481-C-T

http://identifiers.org/hco/5/GRCh38#139651117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965522-C-A

139651117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965522-C-T

http://identifiers.org/hco/5/GRCh38#139651121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965526-C-A

139651121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35965526-C-T

http://identifiers.org/hco/5/GRCh38#139651122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35965527-C-A

139651268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35965625-G-T

139651538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35965857-A-G

139652105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966296-C-T

139652170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966327-G-T

139652171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966328-C-G

139652171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966328-C-T

139652182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966339-G-T

139652359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35966496-C-G

139652461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35966607-C-T

139652979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35967236-G-A

139653030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35967299-C-T

http://identifiers.org/hco/5/GRCh38#139653134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35967358-C-A

139653143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35967367-C-T

139653416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35967601-A-G

139654124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35968339-C-G

139654455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35968787-T-G

139654862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35969290-G-A

139655215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35969656-C-T

139655349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35969750-A-G

http://identifiers.org/hco/5/GRCh38#139655401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35969804-A-C

139655417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35969820-T-C

139655417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35969820-T-G

139655763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35970151-C-T

http://identifiers.org/hco/5/GRCh38#139655766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35970154-C-A

139655782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35970181-T-G

139656028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35970426-C-T

139656191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35970575-T-C

139656457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35970764-A-G

139656511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35970815-T-G

139657328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971257-C-G

139657535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971429-G-C

139657535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971429-G-T

139657536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971430-T-G

139657559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971454-T-G

139657605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971503-G-A

139657665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971549-T-G

139657687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971571-A-G

139657889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971777-T-A

139657889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971777-T-C

139657889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35971777-T-G

http://identifiers.org/hco/5/GRCh38#139658899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35972737-C-A

139658899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35972737-C-T

139659212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35973019-A-G

139659290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35973084-C-T

139659405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35973166-A-G

http://identifiers.org/hco/5/GRCh38#139659607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35973350-C-A

139659632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35973379-A-G

139659632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35973379-A-T

139659788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35973517-G-T

139660265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35973940-G-A

139660351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35974041-G-A

139660417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974106-G-A

139660472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974159-T-C

139660667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974359-C-T

139660684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974375-C-T

139660940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974607-G-A

http://identifiers.org/hco/5/GRCh38#139660996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35974663-A-C

139661000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35974667-A-G

139661108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974762-C-T

139661160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974814-C-T

139661161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35974815-G-A

http://identifiers.org/hco/5/GRCh38#139661427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35975057-C-A

139661427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35975057-C-T

139661430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, undefined
orthologous variants: 35975060-G-A

139661878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35975443-A-G

http://identifiers.org/hco/5/GRCh38#139662307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35975800-A-C

139662677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976064-G-C

139662747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976120-G-A

139662792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976221-G-A

139662861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976364-G-A

139663279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976763-C-T

139663620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35976947-G-A

139664320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35977372-G-A

http://identifiers.org/hco/5/GRCh38#139664459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35977513-C-A

139664858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35977833-C-T

139665456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978450-T-A

139665456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978450-T-C

139665486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978480-C-T

139665502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978496-T-C

139665502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978496-T-G

http://identifiers.org/hco/5/GRCh38#139665548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35978537-A-C

139665598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35978587-G-A

139665598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35978587-G-T

http://identifiers.org/hco/5/GRCh38#139665743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35978734-C-A

139665743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35978734-C-T

139665774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35978766-C-T

139665796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35978788-T-C

139665803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 35978795-G-A

139665844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978827-G-A

139665844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978827-G-T

139665845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978828-G-A

139665845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978828-G-T

139665891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978877-G-A

139665891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978877-G-T

http://identifiers.org/hco/5/GRCh38#139665906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35978904-C-A

139665929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35978925-C-T

139666164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35979082-A-T

139666335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35979215-G-T

139667216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35980308-G-C

139667459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35980524-G-A

139667484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35980549-G-A

139667630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35980658-C-G

139668287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35981221-G-A

139668287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35981221-G-T

139668735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35981559-G-A

http://identifiers.org/hco/5/GRCh38#139669306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35982047-C-A

139670017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35982657-G-C

139670150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35982803-G-A

139670150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35982803-G-C

139670285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35982958-G-A

139670514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35983182-G-A

139670708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35983336-A-G

139671035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35983611-C-T

http://identifiers.org/hco/5/GRCh38#139671127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35983678-C-A

139673193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35985437-A-G

139674741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35987198-G-A

http://identifiers.org/hco/5/GRCh38#139675090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35987460-C-A

139675284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35987615-A-G

http://identifiers.org/hco/5/GRCh38#139675442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35987732-C-A

139675625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35987927-G-A

139675625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35987927-G-T

139675922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988163-G-C

139676101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988295-C-T

http://identifiers.org/hco/5/GRCh38#139676103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35988297-C-A

139676721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988393-G-A

139677052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988655-T-C

139677097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988700-C-T

139677098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988701-G-A

139677209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35988812-C-T

139677423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35989028-G-T

http://identifiers.org/hco/5/GRCh38#139677519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35989121-A-C

139677625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35989238-T-C

139677937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35989555-G-A

139678598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35990120-C-G

139678601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35990123-C-T

139678800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35990404-G-A

139679146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35990694-C-T

139679242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35990769-C-T

139679577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35991006-G-A

139680048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35991171-T-G

139680278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron variant
orthologous variants: 35991381-G-T

139680356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35991438-T-G

http://identifiers.org/hco/5/GRCh38#139680381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35991463-C-A

139680557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: missense variant
orthologous variants: 35991634-G-A

139680557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: missense variant
orthologous variants: 35991634-G-T

139680658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: synonymous variant
orthologous variants: 35991732-A-G

http://identifiers.org/hco/5/GRCh38#139680709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35991783-C-A

139680709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: synonymous variant
orthologous variants: 35991783-C-T

139680786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: missense variant
orthologous variants: 35991860-G-A

139681045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35992107-C-T

139682761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35993604-G-A

139682761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35993604-G-T

139682880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35993720-G-A

139682880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35993720-G-C

139682937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35993785-G-A

139682937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35993785-G-C

139682937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35993785-G-T

139683056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35993906-A-G

139683056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35993906-A-T

139683146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35994006-A-G

http://identifiers.org/hco/5/GRCh38#139683410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35994278-C-A

139683410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35994278-C-T

http://identifiers.org/hco/5/GRCh38#139683725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35994601-C-A

139683725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3 prime UTR variant
orthologous variants: 35994601-C-T

139683749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3 prime UTR variant
orthologous variants: 35994625-G-A

139683749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3 prime UTR variant
orthologous variants: 35994625-G-C

139683749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26943
most severe consequence: 3 prime UTR variant
orthologous variants: 35994625-G-T