http://identifiers.org/hco/8/GRCh38#28494314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#65499808-A-C

28494329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65499793-G-T

http://identifiers.org/hco/8/GRCh38#28494349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65499773-C-A

28494349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65499773-C-T

28494672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65499496-T-C

28494759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65499426-A-G

28494834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65499352-T-C

28495271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65498940-C-T

28495518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65498739-C-T

28495893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65498223-A-G

28497466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65496085-T-C

28497485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65496066-T-C

28497682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495899-A-G

28497838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495775-C-T

28497883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495729-C-G

28497883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495729-C-T

28497939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495675-C-G

28498253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495317-C-G

28498285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495296-C-G

28498285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495296-C-T

28498333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65495246-A-G

28499190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65494030-T-C

http://identifiers.org/hco/8/GRCh38#28499231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65493989-C-A

28499231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65493989-C-G

http://identifiers.org/hco/8/GRCh38#28499499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65493063-A-C

28499499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65493063-A-G

28499558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65492999-A-G

28499614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65492754-A-G

28499802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65492564-T-C

28499849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65492376-C-G

http://identifiers.org/hco/8/GRCh38#28499903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65492264-C-A

28499903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65492264-C-T

28501894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491989-A-G

28501942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491939-T-C

28501945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491936-A-G

http://identifiers.org/hco/8/GRCh38#28502135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65491774-A-C

28502135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491774-A-G

28502135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491774-A-T

28502275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491615-A-G

28502324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491434-T-C

28502347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491354-T-C

28502420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491278-T-C

28502435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65491225-T-C

28502568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490999-G-A

http://identifiers.org/hco/8/GRCh38#28502586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65490980-C-A

28502586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490980-C-T

28502587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490979-A-G

28502613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490957-T-C

http://identifiers.org/hco/8/GRCh38#28502641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65490933-C-A

28502643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490931-C-T

28502729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65490853-T-G

28502837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65490745-C-T

28502854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65490728-T-C

http://identifiers.org/hco/8/GRCh38#28502988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65490605-C-A

28503036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65490557-T-A

28503349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65490269-T-C

28503718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65489608-G-A

28504107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65488810-T-G

28504331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65488588-A-G

28504462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65488474-A-T

28504743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65488231-A-G

28504920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65488079-G-T

28505012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65487997-G-A

28505079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65487935-T-C

28511522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65485694-C-T

28511726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65485462-A-T

28512022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65485219-G-A

28512613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65484545-A-G

28512875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65484350-A-G

http://identifiers.org/hco/8/GRCh38#28513081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65483940-A-C

28513458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65483547-T-C

28513654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65483294-A-G

28513730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65483209-T-G

28514112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65482831-C-G

28514173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65482769-T-C

28514513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65482385-G-A

28514514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65482384-C-T

28514541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65482360-C-T

28515065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65481709-C-T

28518835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65478541-A-G

28519377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65478071-A-G

28519377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65478071-A-T

http://identifiers.org/hco/8/GRCh38#28519441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65477967-A-C

28520275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65477717-T-A

28520577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65477417-T-C

28520769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 65477230-C-T

28521048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65476931-A-G

28524151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65475338-T-C

http://identifiers.org/hco/8/GRCh38#28527121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65473401-A-C

28527151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65473374-C-T

28527265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 65473260-T-C

28527538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65472987-G-A

28527856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65472669-T-C

http://identifiers.org/hco/8/GRCh38#28528223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65472307-C-A

28528223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65472307-C-G

28528223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65472307-C-T

28528620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65471931-T-A

28528913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65471687-C-T

28529399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65471317-T-A

http://identifiers.org/hco/8/GRCh38#28535073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65464003-A-C

28538162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65461610-G-A

28538816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460700-C-T

28538847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460674-T-C

28538950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65460588-G-A

28539276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65458313-G-A

28539334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65458262-A-G

28539610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65457887-A-G

28539736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65457765-T-A

28539848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65457671-A-G

28540168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65457367-T-G

28541040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65456665-G-A

http://identifiers.org/hco/8/GRCh38#28541080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65456636-C-A

28541197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65456540-G-A

28541559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65456186-C-T

http://identifiers.org/hco/8/GRCh38#28541953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65455864-A-C

28542165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455705-C-G

28542165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455705-C-T

28542233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455644-C-T

http://identifiers.org/hco/8/GRCh38#28542342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65455543-C-A

28542822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455379-C-T

28542900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455315-A-G

28543165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65455077-T-G

http://identifiers.org/hco/8/GRCh38#28543318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65454675-C-A

28543319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65454674-C-G

28551570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449703-A-G

28551593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449680-G-A

28551593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449680-G-C

28551618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65449655-C-T

28551681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65449592-G-A

http://identifiers.org/hco/8/GRCh38#28551764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65449511-A-C

28552231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449107-T-G

28552265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449074-C-G

28552287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65449050-C-T

28554815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448423-T-C

28554838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448405-A-G

28554838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65448405-A-T

28555286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447822-T-C

28555682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447432-T-A

28555682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447432-T-C

28555682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447432-T-G

28555688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447426-G-A

28555693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447417-A-G

28555990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447126-G-A

28556000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447116-T-A

28556015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447101-T-C

28556015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447101-T-G

http://identifiers.org/hco/8/GRCh38#28556045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65447074-C-A

28556045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447074-C-T

28556058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447061-G-C

28556058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447061-G-T

http://identifiers.org/hco/8/GRCh38#28556067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65447052-C-A

28556070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447049-A-G

28556073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447046-T-A

28556073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65447046-T-C

28556189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446935-G-A

28556415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446274-T-C

28556543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65446163-T-C

28556898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65445737-G-A

28557946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65444069-T-C

28557975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65444038-G-A

28557991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65444022-T-C

28558161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443869-G-A

28558316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443737-A-G

http://identifiers.org/hco/8/GRCh38#28558739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65443664-A-C

28558774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443631-A-G

28558787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443618-A-G

28559782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443310-T-C

28559944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443214-A-G

28560069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443098-G-A

28560074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443094-A-T

28560148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65443022-G-C

28561270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442708-T-A

http://identifiers.org/hco/8/GRCh38#28561594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65442418-C-A

28561594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65442418-C-T

28562212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440918-A-T

28562268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440866-T-C

28562401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440760-G-C

28562464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440711-C-T

http://identifiers.org/hco/8/GRCh38#28562697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65440476-C-A

28562697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440476-C-T

28562748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65440430-T-C

28563009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 65440168-T-C

28563009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 65440168-T-G

28563628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65439579-G-C

28563653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65439554-G-T

http://identifiers.org/hco/8/GRCh38#28564012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65439199-C-A

28564573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65438664-G-C

28564639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65438582-T-A

http://identifiers.org/hco/8/GRCh38#28565022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65438186-C-A

28565291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65437947-A-G

http://identifiers.org/hco/8/GRCh38#28565411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65437865-C-A

28565682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65437601-T-G

28565683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65437600-T-A

28565859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65437322-G-T

28566005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65437176-T-G

28568186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436898-T-C

28568427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436479-G-A

28568427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436479-G-C

28568427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436479-G-T

28568514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436403-A-G

28568705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436237-A-G

28568726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436216-T-C

28568791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65436166-G-A

http://identifiers.org/hco/8/GRCh38#28568809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65436148-C-A

28569067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65435717-T-C

28569067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65435717-T-G

28569093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65435685-T-C

28569388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65435441-T-A

28569525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65435327-G-T

http://identifiers.org/hco/8/GRCh38#28569528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65435324-C-A

28569987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65434516-G-C

http://identifiers.org/hco/8/GRCh38#28570706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65433812-C-A

28570706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65433812-C-T

28570784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65433733-A-G

28571333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65432866-T-C

28571768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65431962-T-C

http://identifiers.org/hco/8/GRCh38#28571828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65431808-C-A

28571828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65431808-C-T

28572017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65431582-G-A

28573026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430779-A-T

28573040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430765-G-A

28573041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430764-A-G

http://identifiers.org/hco/8/GRCh38#28573160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#65430649-C-A

28573160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430649-C-T

28573215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430596-C-T

28573460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430514-C-G

28574065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4041
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 65430088-T-C