http://identifiers.org/hco/7/GRCh38#7156954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7823233-C-A

7156954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: 7823233-C-T

7157163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: 7823439-T-C

7157226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823495-G-T

7157303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 7823552-T-C

7157359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: 7823606-G-A

7157359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: 7823606-G-T

7157389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5 prime UTR variant
orthologous variants: 7823635-A-G

7157429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823677-G-T

7157457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823700-T-C

7157457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823700-T-G

7157563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823791-C-G

7157661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7823878-G-C

7157767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824004-A-G

7157779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824017-T-C

7157809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824043-A-G

7157810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824044-T-C

http://identifiers.org/hco/7/GRCh38#7157843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7824077-A-C

7157843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824077-A-T

7157918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824143-A-G

http://identifiers.org/hco/7/GRCh38#7157972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7824198-A-C

7158095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7824321-C-G

7167454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7826492-A-G

7167568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7826620-G-A

7167568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7826620-G-C

7176334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7830821-A-G

7176572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, undefined
orthologous variants: 7831048-A-G

7176677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7831149-T-C

7176677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7831149-T-G

7176802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7831271-A-G

http://identifiers.org/hco/7/GRCh38#7177212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#7832258-C-A

7177895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7833246-C-T

7179925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842064-C-G

7179991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842104-C-T

7180025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842133-T-C

7180058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842167-C-T

7180216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842329-G-T

http://identifiers.org/hco/7/GRCh38#7180239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7842352-A-C

7180239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842352-A-G

7180500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842539-T-C

7180547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842567-A-G

7180621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842624-T-G

7181114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7842946-T-G

7181281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7843052-G-A

http://identifiers.org/hco/7/GRCh38#7181401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7843146-C-A

7181435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7843179-T-C

7181502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7843245-G-T

7181753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7843821-C-G

7181961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844099-T-C

7182272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844456-T-C

7182391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844533-G-C

http://identifiers.org/hco/7/GRCh38#7182429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7844571-C-A

7182429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844571-C-T

7182458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844600-C-T

7182459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7844601-T-C

http://identifiers.org/hco/7/GRCh38#7182760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7844928-C-A

7182789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844956-G-A

7182789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844956-G-T

http://identifiers.org/hco/7/GRCh38#7182806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7844973-C-A

7182806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844973-C-T

7182807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844974-G-A

7182807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844974-G-T

7182808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7844975-C-G

http://identifiers.org/hco/7/GRCh38#7182828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7844995-C-A

7182828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7844995-C-G

7182828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7844995-C-T

7183155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845163-C-G

7183155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845163-C-T

7183187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845200-T-G

7183482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845425-G-A

7183482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845425-G-C

7183483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845426-G-T

7183501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7845444-A-T

http://identifiers.org/hco/7/GRCh38#7183651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7845580-C-A

7183651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845580-C-G

7183651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845580-C-T

http://identifiers.org/hco/7/GRCh38#7183732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7845643-C-A

7183732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845643-C-T

7183741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845657-A-G

7183788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845688-C-T

7183861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845734-T-G

7183965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7845847-C-G

7184164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846053-A-G

7184245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846134-C-G

7184355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846222-T-A

7184608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846454-C-T

7184669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7846515-G-C

http://identifiers.org/hco/7/GRCh38#7184702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7846547-A-C

7185373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7847244-G-T

7189061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849510-A-T

7189093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849532-T-C

7189113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849549-A-G

http://identifiers.org/hco/7/GRCh38#7189122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7849558-C-A

http://identifiers.org/hco/7/GRCh38#7189351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7849747-C-A

7189419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7849800-G-A

http://identifiers.org/hco/7/GRCh38#7189449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7849828-A-C

7189705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850070-A-G

7189952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850297-A-G

7189968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850315-A-G

7189982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850329-T-A

7190178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850498-G-A

7190259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7850576-A-G

7191057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851652-G-A

7191124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851718-G-A

http://identifiers.org/hco/7/GRCh38#7191131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7851725-C-A

7191131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851725-C-T

7191200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851786-A-G

7191326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851892-T-C

7191399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7851952-G-A

7191561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852259-T-C

7191629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852326-C-T

7191853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7852506-A-G

7226656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859325-G-C

7226676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859344-A-T

7226700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859364-T-C

7226793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859440-C-G

7226793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859440-C-T

7226971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859532-G-A

7227234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7859778-A-G

7228384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860856-C-T

7228444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860917-G-T

7228479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860946-G-T

7228499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7860962-A-T

7228706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7861143-A-T

7234216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863770-G-A

7234216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863770-G-T

7234247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7863799-C-T

7234285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7863838-T-G

http://identifiers.org/hco/7/GRCh38#7234429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7864031-C-A

7234429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7864031-C-G

http://identifiers.org/hco/7/GRCh38#7234437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7864039-A-C

7234437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7864039-A-G

7234454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7864056-T-A

7234478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7864080-T-C

7234517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7864119-T-C

7234517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7864119-T-G

7237187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7865299-T-C

7237576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7865700-A-T

7237590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7865716-T-A

7237591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7865717-C-G

7237627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7865752-A-G

http://identifiers.org/hco/7/GRCh38#7237963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7866114-A-C

7237963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7866114-A-G

7238020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7866151-A-G

7238050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7866177-G-T

http://identifiers.org/hco/7/GRCh38#7238103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7866232-C-A

http://identifiers.org/hco/7/GRCh38#7238104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7866233-A-C

7238172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7866300-G-T

http://identifiers.org/hco/7/GRCh38#7238322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7866443-C-A

7238337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense variant
orthologous variants: 7866458-G-T

7238364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866485-T-C

7238364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866485-T-G

7238403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866524-A-G

7238403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866524-A-T

7238421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense variant
orthologous variants: 7866542-C-G

7238421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866542-C-T

7238496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7866617-T-C

7238812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense variant
orthologous variants: 7866933-A-G

7238886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: synonymous variant
orthologous variants: 7867007-T-C

7238886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense variant
orthologous variants: 7867007-T-G

7238917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: missense variant
orthologous variants: 7867038-G-A

7239031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7867149-T-C

7239044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7867162-T-A

7239115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7867226-A-G

7239145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7867256-C-T

http://identifiers.org/hco/7/GRCh38#7239379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7868133-C-A

7239379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7868133-C-T

7239559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7868300-T-A

7239561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7868302-G-C

7240469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7868991-A-G

7240605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7869126-G-A

7240729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7869368-C-T

7240756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7869395-G-A

7240841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7869472-C-G

7240845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7869476-C-T

7241588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870122-T-C

7241624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870150-G-A

7243279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870837-T-G

7243298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870848-A-G

7243320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870869-A-G

7243390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870938-A-G

7243390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870938-A-T

7243400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870948-G-A

7243400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870948-G-T

http://identifiers.org/hco/7/GRCh38#7243405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7870953-A-C

7243405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870953-A-G

7243405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: intron variant
orthologous variants: 7870953-A-T

7243739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871269-G-T

7243757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871273-T-A

7243757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871273-T-C

7243799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871308-T-G

7243807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871316-T-A

7243807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871316-T-C

7243910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871423-G-A

7243910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871423-G-T

7244066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871572-T-G

7244298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871763-A-G

http://identifiers.org/hco/7/GRCh38#7244336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7871800-C-A

7244366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7871829-A-G

7244576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872036-G-A

7244576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872036-G-C

http://identifiers.org/hco/7/GRCh38#7244656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7872098-C-A

7244954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872368-T-C

7244956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872370-A-G

7245110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872511-C-T

http://identifiers.org/hco/7/GRCh38#7245200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7872587-A-C

7245745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872906-G-T

7245756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872917-A-G

http://identifiers.org/hco/7/GRCh38#7245805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7872965-C-A

7245805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7872965-C-T

7245849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7873005-A-G

7245866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7873022-G-T

7246261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7873436-T-A

7246434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7873628-T-C

http://identifiers.org/hco/7/GRCh38#7246543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7873724-C-A

7246732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7873854-A-G

7247121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874252-G-A

7247166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874315-G-T

7247201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874336-A-G

7247507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874649-G-A

7247543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874688-A-G

7247584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874745-T-C

http://identifiers.org/hco/7/GRCh38#7247597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7874754-A-C

7247709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7874844-T-C

7247915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875009-G-T

7248137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875197-A-G

7248198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875259-C-T

7248273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875336-A-G

http://identifiers.org/hco/7/GRCh38#7248288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#7875351-C-A

7248353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875421-A-T

7248393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24337
most severe consequence: 3 prime UTR variant
orthologous variants: 7875461-A-G