http://identifiers.org/hco/22/GRCh38#39995303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80556372-C-A

39995303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80556372-C-G

39995303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: synonymous variant
orthologous variants: 80556372-C-T

39995414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80556471-G-A

39995414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 80556471-G-T

http://identifiers.org/hco/22/GRCh38#39995549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80556606-C-A

39995549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556606-C-T

39995561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556618-T-G

39995595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556658-C-G

39995648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556694-G-A

39995648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556694-G-T

39995749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80556776-C-T

39996007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557030-C-G

39996268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557275-C-T

http://identifiers.org/hco/22/GRCh38#39996344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80557350-A-C

39996418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557418-A-G

39996425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557425-G-A

39996425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557425-G-T

39996713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557860-G-A

39996737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80557877-C-G

39997144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80558849-C-G

39997419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559097-G-A

39997441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559119-G-A

39997474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559156-G-A

39997482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559164-C-T

39997741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559401-T-G

39997959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 80559436-G-A

39997959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 80559436-G-C

39997959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 80559436-G-T

http://identifiers.org/hco/22/GRCh38#39998256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80559717-C-A

39998256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559717-C-T

http://identifiers.org/hco/22/GRCh38#39998263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80559719-A-C

39998478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80559888-T-G

http://identifiers.org/hco/22/GRCh38#39998783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80560352-A-C

39998783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80560352-A-G

39998854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560400-A-G

http://identifiers.org/hco/22/GRCh38#39998880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80560430-C-A

39998892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560442-A-G

39998892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560442-A-T

39999011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560543-G-A

39999031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560561-G-A

39999031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80560561-G-T

39999098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 80560612-T-C

39999156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80560669-G-T

39999171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80560684-G-A

39999171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80560684-G-T

39999193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80560706-G-A

39999193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80560706-G-T

39999263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80560756-G-A

http://identifiers.org/hco/22/GRCh38#40000862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80561936-A-C

40000862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80561936-A-G

40000927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562012-C-T

40001033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562120-A-G

40001056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562134-T-C

40001074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562158-T-G

40001787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562511-C-T

40001894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562573-T-C

40002101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562730-G-T

40002295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80562908-T-A

http://identifiers.org/hco/22/GRCh38#40002443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80563061-C-A

40002739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80563298-T-C

40002934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80563438-A-G

40003036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80563515-G-A

40003726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80564133-A-G

40004041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80564413-G-A

http://identifiers.org/hco/22/GRCh38#40004904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80564849-C-A

40005063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80565032-A-G

40005184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80565151-A-G

40005187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80565154-A-G

40005188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80565155-A-G

40005515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80565503-C-T

40006482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566132-A-T

40006753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566393-G-T

40006893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566525-G-A

40007123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566745-C-G

40007123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566745-C-T

40007164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566787-G-C

40007165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80566788-T-G

40008575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567192-C-T

40008599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567216-C-T

40008600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567217-G-A

40008600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567217-G-C

40008600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567217-G-T

40008789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80567393-C-G

40008789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80567393-C-T

40008827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567428-G-A

40008953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567556-C-G

40008953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567556-C-T

40009164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80567752-G-A

40009216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567793-A-G

40009216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80567793-A-T

http://identifiers.org/hco/22/GRCh38#40009558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80569459-C-A

40009558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80569459-C-T

40009574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80569479-T-C

40009587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80569492-G-A

40009587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80569492-G-T

40009699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80569598-G-A

40009699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80569598-G-T

40009725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80569628-G-A

40009725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80569628-G-T

40009774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80569670-G-T

40010152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570044-G-A

40010152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570044-G-T

40010153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570045-C-T

40010160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570052-G-A

40010160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570052-G-T

http://identifiers.org/hco/22/GRCh38#40010207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80570100-C-A

40010207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570100-C-T

40010510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570439-G-A

40010579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570504-G-A

40010579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570504-G-T

40010583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570508-A-G

40010692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570594-C-T

40010757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80570662-C-T

40010991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80570897-G-T

40011180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80571081-A-G

40011180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80571081-A-T

40011373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80571264-C-T

40011779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80571564-T-C

40014828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80571945-T-C

40015632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80572738-C-G

40017635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80573255-G-A

40018895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80573847-C-T

40018913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80573865-T-C

40019016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80573962-A-G

http://identifiers.org/hco/22/GRCh38#40019115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80574066-C-A

40019115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574066-C-T

http://identifiers.org/hco/22/GRCh38#40019125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80574076-C-A

40019125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574076-C-T

40019469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574381-T-G

40019600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574499-G-A

40019835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574675-G-T

40019846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574686-G-T

40019859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574705-T-C

40019859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80574705-T-G

40020200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575047-T-C

40020365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575188-T-C

40020386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575209-G-A

40020386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575209-G-T

http://identifiers.org/hco/22/GRCh38#40020388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80575211-A-C

40020388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575211-A-G

40020388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575211-A-T

40020395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575213-C-T

40020766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575651-C-T

40020923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575786-T-C

http://identifiers.org/hco/22/GRCh38#40021159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80575971-C-A

40021159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575971-C-T

40021162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80575974-G-T

40021250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80576077-T-A

40021250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80576077-T-C

40021274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80576104-G-T

40021383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: synonymous variant
orthologous variants: 80576205-G-C

40021513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576335-C-T

40021557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: synonymous variant
orthologous variants: 80576379-G-A

40021717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576539-A-G

40021874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576705-G-A

40021874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576705-G-C

40021874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576705-G-T

40021949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576783-G-A

40021949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576783-G-C

40021949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: missense variant
orthologous variants: 80576783-G-T

40022075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80576863-G-A

40022075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80576863-G-T

40022217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80577002-T-A

40022889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80577433-C-T

40023298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80577671-G-A

40023652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80577964-G-A

40024618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80578583-G-A

40024625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80578590-G-A

40024897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80578847-C-G

40024897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80578847-C-T

http://identifiers.org/hco/22/GRCh38#40024928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80578867-C-A

http://identifiers.org/hco/22/GRCh38#40024941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80578894-C-A

40024941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80578894-C-T

40025012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80578965-G-A

40025013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron_variant, undefined
orthologous variants: 80578966-C-T

40025134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579067-A-G

40025140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579073-C-T

40025145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579078-C-T

40025279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579169-G-T

40025823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579645-C-T

40025830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579652-G-A

40025893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579706-T-A

40026118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579916-G-A

40026118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80579916-G-T

40026455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80580213-G-C

40026827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80580437-G-A

40026938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80580548-C-G

40027017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80580595-G-A

40027287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80580852-A-G

40027442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581132-T-C

40027544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581268-T-C

40027647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581376-G-C

40027766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581477-G-A

40027813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581568-C-G

40027869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581708-T-A

40027869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581708-T-C

http://identifiers.org/hco/22/GRCh38#40027879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80581721-A-C

40027913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80581753-G-A

40028453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80582313-A-G

40028917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80582705-G-A

40028930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80582718-C-T

40029325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80582997-C-T

40029388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80583056-T-G

http://identifiers.org/hco/22/GRCh38#40029434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583097-A-C

40029434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80583097-A-G

40029444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: intron variant
orthologous variants: 80583105-G-A

40029590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583216-C-T

http://identifiers.org/hco/22/GRCh38#40029697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583327-C-A

http://identifiers.org/hco/22/GRCh38#40029734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583362-C-A

40029734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583362-C-T

http://identifiers.org/hco/22/GRCh38#40029755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583396-C-A

40029755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583396-C-T

http://identifiers.org/hco/22/GRCh38#40029759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583400-C-A

40029759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583400-C-T

40029767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583408-T-A

40029785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583425-G-A

40029785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583425-G-C

40029785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583425-G-T

http://identifiers.org/hco/22/GRCh38#40029793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583433-C-A

40029793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583433-C-T

40029823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583457-G-A

40029823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583457-G-T

http://identifiers.org/hco/22/GRCh38#40029852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583505-C-A

40029852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583505-C-T

40029905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583557-T-C

40029912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583564-T-C

http://identifiers.org/hco/22/GRCh38#40029920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583572-C-A

40029920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583572-C-T

40029941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583593-C-T

http://identifiers.org/hco/22/GRCh38#40029990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583634-C-A

40029990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583634-C-T

40029997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583641-G-A

40029997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583641-G-T

40030086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583699-G-A

40030086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583699-G-T

40030092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583705-G-A

40030132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583745-C-T

http://identifiers.org/hco/22/GRCh38#40030297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583898-C-A

40030297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583898-C-T

http://identifiers.org/hco/22/GRCh38#40030305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80583906-C-A

40030305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583906-C-T

40030307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583908-G-A

40030307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80583908-G-T

40030461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584020-G-T

40030601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584149-A-G

40030646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584174-G-T

40030690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584209-G-T

http://identifiers.org/hco/22/GRCh38#40030801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80584305-C-A

40030801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584305-C-T

40030802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584306-A-G

http://identifiers.org/hco/22/GRCh38#40030875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80584368-C-A

40030875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584368-C-G

40030875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584368-C-T

http://identifiers.org/hco/22/GRCh38#40030884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80584377-C-A

40031082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584533-G-T

40031207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584630-G-T

40031256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584678-G-A

40031263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584685-G-T

http://identifiers.org/hco/22/GRCh38#40031289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80584697-C-A

40031289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584697-C-G

40031289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80584697-C-T

40033796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80585920-C-T

40033818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80585940-C-G

40034026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586139-C-T

40034060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586173-T-A

40034060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586173-T-C

40034077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586189-C-G

40034077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586189-C-T

40034078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586190-T-C

40034108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586220-A-G

http://identifiers.org/hco/22/GRCh38#40034143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80586255-C-A

40034147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586259-T-C

40034238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586348-T-A

40034283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586393-T-A

40034283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586393-T-C

http://identifiers.org/hco/22/GRCh38#40034329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80586438-C-A

40034332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586441-A-G

40034361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586470-G-A

40034361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586470-G-T

40034404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586525-G-T

40034412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586533-G-T

40034429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586549-T-C

40034480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586595-C-T

40034482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586597-T-C

40034484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586599-G-A

40034484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586599-G-T

40034493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586612-G-A

40034493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586612-G-T

40034494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586613-C-T

40034518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586637-A-G

40034562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586681-T-C

http://identifiers.org/hco/22/GRCh38#40034589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80586710-C-A

40034601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586722-G-T

http://identifiers.org/hco/22/GRCh38#40034646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80586749-C-A

40034646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80586749-C-T

40035043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587014-G-A

40035043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587014-G-T

40035141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587118-G-T

40035175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587152-G-A

40035210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587187-T-C

40035236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587210-A-G

40035271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587245-A-G

40035271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587245-A-T

40035530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587473-G-T

40035542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587485-G-A

40035542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80587485-G-T

40036339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80588021-G-T

40036382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80588050-C-T

40036499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80588172-G-A

40036510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80588183-C-T

40036798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -A-G

40036798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -A-T

http://identifiers.org/hco/22/GRCh38#40036852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: -C-A

40039290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589808-A-G

http://identifiers.org/hco/22/GRCh38#40039306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80589824-C-A

40039306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589824-C-T

40039317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589835-G-T

40039321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589839-G-A

40039321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589839-G-T

40039354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589893-C-G

40039354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589893-C-T

40039371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589909-G-T

40039389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589924-A-G

40039392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80589927-A-G

40039626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590085-G-T

40039761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590186-A-G

40039761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590186-A-T

40039883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590312-G-T

40039922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590342-T-C

40039938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590358-G-A

40039938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590358-G-T

40039953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590373-G-T

40039997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590421-G-T

40040050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590460-A-G

http://identifiers.org/hco/22/GRCh38#40040056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80590466-C-A

40040172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590590-G-A

40040172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590590-G-T

40040209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590637-G-A

40040209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590637-G-T

40040231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590657-T-C

40040376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590795-G-A

40040427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590846-G-A

40040445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590864-G-A

40040445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590864-G-C

40040446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590865-T-C

40040453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590872-T-C

40040506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590923-G-A

40040506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590923-G-T

40040507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80590924-G-A

40040737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591161-C-T

40040787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591203-G-T

http://identifiers.org/hco/22/GRCh38#40040909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#80591321-C-A

40040919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591331-A-G

40040923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591335-A-G

40040946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591358-G-A

40040948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591360-T-A

40040954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591366-T-C

http://identifiers.org/hco/22/GRCh38#40040963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80591372-C-A

40040963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591372-C-T

40041092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591502-G-A

40041092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591502-G-T

40041418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591796-C-T

http://identifiers.org/hco/22/GRCh38#40041425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80591803-C-A

40041425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591803-C-T

http://identifiers.org/hco/22/GRCh38#40041534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80591930-C-A

40041534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80591930-C-T

40041865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592255-G-A

40041865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592255-G-C

40041865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592255-G-T

40041879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592277-T-C

40041904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592302-G-A

40041904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592302-G-T

40041940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592313-C-T

40041967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592328-T-C

40041972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592333-C-T

40041992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592345-G-T

http://identifiers.org/hco/22/GRCh38#40042350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80592786-C-A

40042350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592786-C-T

http://identifiers.org/hco/22/GRCh38#40042431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80592864-A-C

40042431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592864-A-G

40042439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592872-G-A

40042439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80592872-G-T

http://identifiers.org/hco/22/GRCh38#40042449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80592881-C-A

40042594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80593014-T-C

40042971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80593636-G-A

40043026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3 prime UTR variant
orthologous variants: 80593691-C-T

40043195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80593855-G-A

40043195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80593855-G-T

http://identifiers.org/hco/22/GRCh38#40043315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80593968-C-A

http://identifiers.org/hco/22/GRCh38#40043456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25148
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80594123-C-A