38419359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5 prime UTR variant
orthologous variants: 97295317-G-A

38419364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5 prime UTR variant
orthologous variants: 97295322-G-A

38419364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5 prime UTR variant
orthologous variants: 97295322-G-T

38419411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295368-C-T

38419419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295376-G-A

38419419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295376-G-C

38419419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295376-G-T

38419421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295378-G-A

38419421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295378-G-T

38419596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295548-A-G

http://identifiers.org/hco/17/GRCh38#38419597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97295549-C-A

38420093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97295999-G-T

38420303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296194-C-T

38420353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296243-C-T

38420368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296259-A-G

38420525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296407-G-T

38420840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296675-G-A

38420840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296675-G-C

38420848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296683-A-G

38420848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296683-A-T

38420856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296686-G-A

38420907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296737-G-A

38420953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296774-G-A

38420963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97296784-C-T

38421390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97297178-A-G

38421980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97297809-G-A

38421980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97297809-G-C

38422127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97297915-C-T

38422163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97297948-C-T

38422409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97298181-G-A

38422901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97298739-T-G

38422967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97298864-A-G

38423000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97298892-C-T

http://identifiers.org/hco/17/GRCh38#38423162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97299075-A-C

38423215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299181-C-T

38423248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299268-C-T

38423267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299287-A-T

http://identifiers.org/hco/17/GRCh38#38423519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97299502-A-C

38423519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299502-A-G

38423519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299502-A-T

http://identifiers.org/hco/17/GRCh38#38423522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97299505-C-A

38423522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97299505-C-T

38423871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, undefined
orthologous variants: 97299268-C-G

38424362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97302038-T-G

38424412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97302083-G-A

38424495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97302169-T-C

38424818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97304262-A-G

http://identifiers.org/hco/17/GRCh38#38424839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97304233-C-A

38424839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97304233-C-T

38425207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303836-T-G

38425214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303829-T-C

38425267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303802-G-A

38425267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303802-G-C

38425267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303802-G-T

38425273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303795-T-C

38425452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303602-C-T

http://identifiers.org/hco/17/GRCh38#38425470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97303584-C-A

38425762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97303301-G-A

38427137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97305115-T-C

38427137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97305115-T-G

38427569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97305227-G-A

38428022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306000-C-G

38428277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306221-C-G

38428282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306224-G-T

38428284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306226-A-G

38428284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306226-A-T

38428341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306300-T-A

38428341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306300-T-G

38428347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306305-G-C

38428347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306305-G-T

http://identifiers.org/hco/17/GRCh38#38428371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306326-A-C

38428371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306326-A-G

38428371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306326-A-T

http://identifiers.org/hco/17/GRCh38#38428372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306327-C-A

38428372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306327-C-T

http://identifiers.org/hco/17/GRCh38#38428435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306380-C-A

38428435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306380-C-T

http://identifiers.org/hco/17/GRCh38#38428463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306408-C-A

38428463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306408-C-G

38428463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97306408-C-T

http://identifiers.org/hco/17/GRCh38#38428465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306410-C-A

38428465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97306410-C-T

http://identifiers.org/hco/17/GRCh38#38428524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97306469-C-A

38428524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97306469-C-T

38428575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97306525-G-A

38428575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97306525-G-T

38428902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97306782-C-T

38429279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307069-C-G

38429988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307738-C-G

38429988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307738-C-T

38430000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307749-C-T

38430518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308624-G-A

38430608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308744-G-A

38430823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309090-G-C

38431025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309340-A-G

38431112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309405-C-G

http://identifiers.org/hco/17/GRCh38#38431158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97309428-C-A

38431667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309933-G-T

38431691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309960-G-A

38432084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97310302-A-G

38433684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97313093-A-G

38434205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97313361-G-T

38434230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97313381-G-A

38434327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97313473-T-A

http://identifiers.org/hco/17/GRCh38#38434509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97313641-C-A

38434909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314011-G-T

38434922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314039-G-A

38434981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314099-C-T

38435036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314177-G-C

38435396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314484-G-C

38435510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97314586-A-G

38436058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97315125-G-A

38436211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97315231-A-G

38436256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97315269-C-G

38436350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97315361-G-A

38436422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97315409-C-T

38440265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318308-G-A

38440368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318409-G-T

38440466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318508-T-C

38440526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318574-C-T

38440680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318711-G-A

38440680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97318711-G-T

38441522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97319460-A-T

38442543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97320379-G-A

38442803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97320681-A-G

38442892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97320762-G-A

38443544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97322181-T-C

38444588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97323209-C-T

38444596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97323217-G-A

http://identifiers.org/hco/17/GRCh38#38447619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97325622-C-A

38447802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97325737-C-T

38448149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97326037-G-A

http://identifiers.org/hco/17/GRCh38#38448320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97326177-C-A

38449288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97326565-C-T

38449680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97326904-G-A

http://identifiers.org/hco/17/GRCh38#38451056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97328766-C-A

38451056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97328766-C-T

38451182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97328879-G-A

38451182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97328879-G-T

http://identifiers.org/hco/17/GRCh38#38451222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97328931-C-A

38451222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97328931-C-G

38451222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97328931-C-T

38451592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329480-G-T

38451999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97329867-A-G

38452030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329898-G-A

38452030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329898-G-C

38452030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329898-G-T

38452043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329910-G-A

38452043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97329910-G-T

38452176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97329998-T-A

38452176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97329998-T-C

38452488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330123-G-T

38452490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330125-C-T

38452592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330147-G-T

38452669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330179-G-T

38452936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330423-G-C

38453161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330654-A-T

38453408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330822-C-G

38453430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330836-T-C

38453430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97330836-T-G

38453733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97331063-G-A

38453903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97331227-G-T

38454176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97331494-G-A

38454202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97331519-G-A

38454202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97331519-G-T

38454235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97331542-T-C

38454689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97332001-G-A

38454765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97332076-A-G

38454785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97332091-G-T

38454815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97332127-T-G

http://identifiers.org/hco/17/GRCh38#38454833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97332145-A-C

38455016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97332313-C-T

38455248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97332547-G-A

38456432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97333665-G-C

38456443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97333676-C-T

38456666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97333839-G-A

http://identifiers.org/hco/17/GRCh38#38457286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334149-C-A

38457318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334181-T-C

http://identifiers.org/hco/17/GRCh38#38457329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334192-C-A

38457329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334192-C-T

http://identifiers.org/hco/17/GRCh38#38457342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334205-A-C

38457342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334205-A-G

38457442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334298-G-A

38457442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334298-G-T

http://identifiers.org/hco/17/GRCh38#38457466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334321-C-A

38457466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334321-C-T

38457517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334378-C-T

http://identifiers.org/hco/17/GRCh38#38457518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334379-A-C

38457636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334591-G-A

38457636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334591-G-T

38457643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334598-G-T

38457695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97334643-T-A

38457884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334780-G-A

38457884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334780-G-C

http://identifiers.org/hco/17/GRCh38#38457964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97334847-C-A

38457964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334847-C-T

38457988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334883-G-T

38457990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334885-G-A

38457990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334885-G-T

38458028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334922-C-T

38458033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334927-G-C

38458068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97334970-C-T

http://identifiers.org/hco/17/GRCh38#38458245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97335153-C-A

38458245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97335153-C-G

38458245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97335153-C-T

38458290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335197-T-C

38458370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335266-T-A

38458370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335266-T-C

http://identifiers.org/hco/17/GRCh38#38458372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97335268-C-A

38459000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335746-G-C

38459060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335796-G-A

38459075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97335811-G-A

38459322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336039-G-T

38459328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336045-A-G

38459617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336285-G-A

38459805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336464-C-T

38460241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336809-C-T

38460449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97336961-G-A

38460702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97337137-G-A

38460804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97337233-G-A

38460804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97337233-G-C

38460804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97337233-G-T

38460841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337273-C-G

38460841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337273-C-T

38460863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337294-G-C

38460863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337294-G-T

38460899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97337329-C-G

38461271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337653-G-A

38461277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337661-C-G

38461278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337662-A-G

38461365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337750-A-G

38461424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337805-C-G

38461424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97337805-C-T

http://identifiers.org/hco/17/GRCh38#38461449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97337831-A-C

38461937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97338733-A-G

38462898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97339048-T-C

38462922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97339072-T-C

38463150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97339303-G-A

38463150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97339303-G-T

38463217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97339374-G-A

38463256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97339409-C-T

38463371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97339522-A-G

38464051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97340107-C-T

38464099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97340164-C-T

http://identifiers.org/hco/17/GRCh38#38464415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97340458-C-A

38464610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97340662-C-T

38464949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97340971-A-T

38465090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97341104-C-G

38465090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97341104-C-T

38465196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97341203-C-T

38465225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97341234-T-G

38465232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97341241-G-A

38465422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97341411-G-A

38466065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97342120-C-T

38466127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97342178-T-C

38466127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97342178-T-G

38466342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342393-G-A

38466342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342393-G-T

http://identifiers.org/hco/17/GRCh38#38466437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97342488-C-A

38466437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342488-C-G

38466437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342488-C-T

http://identifiers.org/hco/17/GRCh38#38466458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97342509-C-A

38466458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342509-C-T

38466715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97342766-G-A

38466715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342766-G-C

38466715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342766-G-T

38466899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97342944-T-G

38467174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97343219-G-A

38467174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97343219-G-C

http://identifiers.org/hco/17/GRCh38#38467299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97343338-C-A

38467299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97343338-C-T

http://identifiers.org/hco/17/GRCh38#38467399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97343405-C-A

38467399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97343405-C-T

http://identifiers.org/hco/17/GRCh38#38467480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97343478-C-A

38467480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97343478-C-G

38467480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97343478-C-T

38467935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97343780-C-T

38468712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344354-C-T

38468966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344551-A-G

38469001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344580-G-A

38469001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344580-G-T

38469035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344609-A-G

38469035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344609-A-T

38469045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344616-G-A

http://identifiers.org/hco/17/GRCh38#38469073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97344646-C-A

38469140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97344687-A-G

38469205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97344752-C-T

http://identifiers.org/hco/17/GRCh38#38469253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97344800-C-A

38469253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97344800-C-T

38469362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344899-G-T

38469363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344900-T-C

38469459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97344974-G-T

http://identifiers.org/hco/17/GRCh38#38469494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97345010-C-A

38469494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97345010-C-T

http://identifiers.org/hco/17/GRCh38#38469504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97345020-C-A

38469504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97345020-C-G

38469504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97345020-C-T

38469505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97345021-G-A

38469528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97345044-C-T

38469546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97345062-C-T

38471208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97346625-T-C

38471242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97346678-C-T

38471248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97346684-C-T

http://identifiers.org/hco/17/GRCh38#38471771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97347189-C-A

38471771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347189-C-G

38471771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347189-C-T

http://identifiers.org/hco/17/GRCh38#38471796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97347214-C-A

38471796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347214-C-T

38472113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347566-T-C

http://identifiers.org/hco/17/GRCh38#38472304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97347730-C-A

38472304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347730-C-T

38472383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347778-G-C

38472550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97347905-T-A

38472666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97348005-G-C

38472752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97348069-T-A

38474270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97349524-T-C

http://identifiers.org/hco/17/GRCh38#38475236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97350466-A-C

38475321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97350551-G-A

38475321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97350551-G-T

38477031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97353454-G-A

38477031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97353454-G-T

38477217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97353652-G-C

38477262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97353731-T-C

http://identifiers.org/hco/17/GRCh38#38477542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97354172-C-A

38477542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97354172-C-T

38477969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97354624-G-A

38477969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97354624-G-T

http://identifiers.org/hco/17/GRCh38#38478001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97354655-A-C

http://identifiers.org/hco/17/GRCh38#38478041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97354682-C-A

38479144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355328-G-A

38479386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355565-G-A

38479387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355566-G-A

38479387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355566-G-T

38479398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355577-G-T

38479425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97355603-T-C

38479554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97355725-G-A

http://identifiers.org/hco/17/GRCh38#38479626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97355764-C-A

38479626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97355764-C-G

38479626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97355764-C-T

http://identifiers.org/hco/17/GRCh38#38479637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97355775-C-A

38479846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 97355978-T-C

38479916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356025-G-A

38479943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356056-G-A

38479943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356056-G-T

38479962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356088-G-A

38479962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356088-G-T

38479981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356108-G-A

38479981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356108-G-T

38479983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356110-G-A

38479983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356110-G-T

38480032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356162-C-T

38480216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356334-C-T

38481845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356676-G-A

http://identifiers.org/hco/17/GRCh38#38481986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97356794-C-A

38481986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97356794-C-T

38482087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 97356901-G-A

38482087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 97356901-G-T

38482151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 97356965-T-C

http://identifiers.org/hco/17/GRCh38#38482155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97356969-C-A

38482155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97356969-C-T

38482186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, undefined
orthologous variants: 97356998-A-G

38482226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357032-C-G

38482228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357034-G-T

38482374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357121-T-C

38482398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357144-G-A

38482398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357144-G-T

38482426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357168-T-C

38482426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97357168-T-G

38482685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 97357420-G-A

38482685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 97357420-G-T

38483064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97357811-C-G

38483228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97358015-T-C

38483261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97358058-A-T

38483447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97358222-G-A

38483885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97358903-C-T

38483982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97358984-G-A

38483999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359000-C-T

38484098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359089-G-C

38484117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359117-G-A

http://identifiers.org/hco/17/GRCh38#38484156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97359157-A-C

38484164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359165-G-A

38484273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359232-G-T

38484801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359705-T-C

38484972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359862-C-G

38484972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359862-C-T

38485089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97359969-G-T

38485173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97360044-T-A

38485211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97360083-C-T

38485273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97360161-A-G

38485437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97360538-C-T

38485516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97360665-G-A

38485516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97360665-G-T

38485661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97360780-G-A

38485903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97361031-A-T

38485994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97361127-T-G

38486043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97361175-C-T

38486163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97361295-G-T

http://identifiers.org/hco/17/GRCh38#38486191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97361322-A-C

38486203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97361341-A-G

38486203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97361341-A-T

38487115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362261-C-T

38487222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362309-C-T

38487304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362353-C-T

38487312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362361-G-A

38487397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362426-A-G

38487397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97362426-A-T

38489078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97364385-A-G

38489118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97364418-A-G

http://identifiers.org/hco/17/GRCh38#38489693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365550-C-A

38489705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97365567-G-A

38489705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97365567-G-T

38489813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97365666-C-T

http://identifiers.org/hco/17/GRCh38#38489819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365672-C-A

38489819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97365672-C-G

http://identifiers.org/hco/17/GRCh38#38489844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365697-C-A

38489853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97365703-T-C

38489865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97365714-A-G

38490098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 97365837-C-G

38490163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: synonymous variant
orthologous variants: 97365902-G-A

38490163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: synonymous variant
orthologous variants: 97365902-G-T

http://identifiers.org/hco/17/GRCh38#38490213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365948-C-A

38490213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365948-C-T

38490215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365950-G-A

38490215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365950-G-T

38490223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365954-A-T

http://identifiers.org/hco/17/GRCh38#38490225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365956-C-A

38490225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365956-C-T

http://identifiers.org/hco/17/GRCh38#38490287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365982-C-A

38490287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365982-C-G

38490287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365982-C-T

http://identifiers.org/hco/17/GRCh38#38490297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97365992-C-A

38490297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365992-C-T

38490303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365998-G-A

38490303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365998-G-C

38490303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97365998-G-T

38490314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366009-C-T

38490318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366013-T-C

38490334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366027-G-A

38490337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366030-G-A

38490337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366030-G-T

38490345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366038-G-C

38490345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366038-G-T

http://identifiers.org/hco/17/GRCh38#38490361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97366053-C-A

38490361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366053-C-G

38490393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97366085-A-G

http://identifiers.org/hco/17/GRCh38#38490656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97366316-C-A

38490656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366316-C-T

http://identifiers.org/hco/17/GRCh38#38490663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97366321-C-A

38490663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366321-C-T

http://identifiers.org/hco/17/GRCh38#38490668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97366326-C-A

38490668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366326-C-T

38490721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366392-T-C

38490742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366413-C-T

38490752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366422-G-C

38490794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366463-A-G

38490829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366498-C-G

38490829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366498-C-T

38490830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366499-G-A

38491249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366731-C-T

38491382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97366841-G-A

38491543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367010-G-T

38491683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367108-A-G

38491693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367118-G-A

38491693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367118-G-T

38491716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367138-A-G

38491716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97367138-A-T

38491763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367162-G-A

38491763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367162-G-T

38491829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367205-A-T

38491839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367216-T-A

38491839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367216-T-C

38491839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367216-T-G

38491844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367221-G-A

38491844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367221-G-T

38491915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367285-C-T

38492064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, undefined
orthologous variants: 97367380-C-T

38492098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, undefined
orthologous variants: 97367405-C-T

38492606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367956-T-G

38492626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367967-A-G

38492647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97367986-G-A

38492750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97368075-G-A

38492883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97368187-T-C

38493544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97368517-G-A

38497257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97380424-G-A

38497438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97380628-G-A

38497715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97380822-G-T

http://identifiers.org/hco/17/GRCh38#38497717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97380824-A-C

38497717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97380824-A-G

38497836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97380958-G-A

38497875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381012-G-T

38497886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381019-T-A

38497886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381019-T-G

38497906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381037-G-A

38497906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381037-G-T

38498033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381688-G-A

38498316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381868-G-T

http://identifiers.org/hco/17/GRCh38#38498373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97381926-C-A

38498373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97381926-C-T

38498530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382076-A-G

38498549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382086-G-A

38498549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382086-G-T

38498601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382138-T-C

38498735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382268-G-T

38498741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382280-A-G

38498778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382317-G-A

38498787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382326-T-C

http://identifiers.org/hco/17/GRCh38#38499076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97382617-A-C

http://identifiers.org/hco/17/GRCh38#38499097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97382638-A-C

38499097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97382638-A-G

38499646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383040-T-G

38499688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383082-G-A

38499688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383082-G-C

38499863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383239-C-T

http://identifiers.org/hco/17/GRCh38#38500303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97383634-C-A

38500303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383634-C-T

38500304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron variant
orthologous variants: 97383635-T-C

38500358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97383690-G-A

38500487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97383808-A-G

38500487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97383808-A-T

38500499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97383820-T-A

38500499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97383820-T-C

http://identifiers.org/hco/17/GRCh38#38500508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97383828-C-A

http://identifiers.org/hco/17/GRCh38#38500678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97383957-A-C

38500678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97383957-A-G

38500682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97383961-T-C

http://identifiers.org/hco/17/GRCh38#38500899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97384166-C-A

38500899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97384166-C-G

38500904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97384171-G-T

http://identifiers.org/hco/17/GRCh38#38500932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97384185-C-A

38500932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97384185-C-T

38501229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97384658-G-A

38501229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97384658-G-T

38503872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97388145-G-A

38503946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97388171-G-C

38504122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97388341-A-G

38504304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97388499-G-A

http://identifiers.org/hco/17/GRCh38#38504323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97388517-A-C

38504407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97388560-T-C

38508331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390188-T-G

38508624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390424-A-G

http://identifiers.org/hco/17/GRCh38#38509839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97390854-C-A

38509839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97390854-C-T

38509864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97390877-T-C

38509878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390888-G-A

38509878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390888-G-T

http://identifiers.org/hco/17/GRCh38#38509916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97390907-C-A

38509916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97390907-C-T

38509926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390917-G-A

38509926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390917-G-C

38509926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97390917-G-T

http://identifiers.org/hco/17/GRCh38#38510012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391003-C-A

38510012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97391003-C-T

http://identifiers.org/hco/17/GRCh38#38510018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391009-C-A

38510018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97391009-C-T

http://identifiers.org/hco/17/GRCh38#38510054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391045-C-A

38510054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97391045-C-G

38510054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97391045-C-T

http://identifiers.org/hco/17/GRCh38#38510159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: stop_gained, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391135-C-A

38510159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 97391135-C-G

38510159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 97391135-C-T

http://identifiers.org/hco/17/GRCh38#38510163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391139-C-A

38510163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 97391139-C-T

38510393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391363-G-A

38510393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391363-G-C

38510393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391363-G-T

http://identifiers.org/hco/17/GRCh38#38510494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391464-C-A

38510494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 97391464-C-T

38510505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 97391487-G-A

38510505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 97391487-G-T

38510519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391501-G-A

38510519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391501-G-C

38510519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391501-G-T

38510570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391552-G-A

38510570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391552-G-T

38510582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391564-G-A

38510582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391564-G-C

38510582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391564-G-T

http://identifiers.org/hco/17/GRCh38#38510585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391573-C-A

38510585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391573-C-T

http://identifiers.org/hco/17/GRCh38#38510588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391576-C-A

38510588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391576-C-G

38510588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391576-C-T

38510757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391745-G-A

38510757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 97391745-G-T

http://identifiers.org/hco/17/GRCh38#38510788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391776-C-A

38510788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391776-C-G

38510788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391776-C-T

http://identifiers.org/hco/17/GRCh38#38510793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391781-C-A

38510793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391781-C-T

http://identifiers.org/hco/17/GRCh38#38510801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391789-C-A

38510801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391789-C-T

38510900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391879-C-G

38510900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 97391879-C-T

http://identifiers.org/hco/17/GRCh38#38510932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97391911-C-A

38510932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391911-C-G

38510932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 97391911-C-T

38510973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97391952-T-C

38510987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97391971-G-A

38511120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392068-G-A

38511120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392068-G-T

38511147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392096-G-A

38511147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392096-G-C

38511147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392096-G-T

38511151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392100-G-A

38511151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392100-G-T

http://identifiers.org/hco/17/GRCh38#38511248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97392172-C-A

38511248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392172-C-T

http://identifiers.org/hco/17/GRCh38#38511385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97392293-C-A

http://identifiers.org/hco/17/GRCh38#38511397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97392314-C-A

38511440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392357-G-A

38511440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392357-G-T

38511498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392454-T-C

http://identifiers.org/hco/17/GRCh38#38511588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97392530-C-A

38511588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392530-C-G

38511588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392530-C-T

38511774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392687-A-G

38511821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392720-C-G

38511821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392720-C-T

38511822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392721-A-G

38511838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392736-G-C

38511947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392811-G-A

http://identifiers.org/hco/17/GRCh38#38511971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97392830-C-A

38511973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392832-C-T

38511988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392847-G-A

38511988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29293
most severe consequence: 3 prime UTR variant
orthologous variants: 97392847-G-T