25351621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3670024-G-A

25351621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3670024-G-C

25351621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3670024-G-T

25351773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3670177-G-A

http://identifiers.org/hco/22/GRCh38#25351935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3670332-A-C

25351935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3670332-A-G

25351964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3670357-G-A

25351964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3670357-G-C

25351964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3670357-G-T

25354260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672203-T-G

http://identifiers.org/hco/22/GRCh38#25354464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672385-C-A

25354464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672385-C-T

http://identifiers.org/hco/22/GRCh38#25354485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672406-C-A

25354485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672406-C-T

25354493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672414-G-A

25354493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672414-G-T

25354666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3672580-G-C

25354714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3672628-G-A

25354798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3672712-A-G

http://identifiers.org/hco/22/GRCh38#25354877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672792-C-A

25354877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672792-C-G

25354877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672792-C-T

http://identifiers.org/hco/22/GRCh38#25354895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672810-C-A

25354895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672810-C-T

http://identifiers.org/hco/22/GRCh38#25354929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672821-C-A

http://identifiers.org/hco/22/GRCh38#25354933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672825-A-C

25354933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3672825-A-G

http://identifiers.org/hco/22/GRCh38#25354938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3672830-C-A

25357120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678085-G-A

25357120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678085-G-T

http://identifiers.org/hco/22/GRCh38#25357123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3678088-C-A

25357123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678088-C-T

25357138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678103-G-A

25357138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678103-G-T

25357144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678109-G-A

25357153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678118-A-G

25357159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678124-G-A

25357159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678124-G-T

25357168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678133-G-A

25357168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678133-G-C

25357168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678133-G-T

http://identifiers.org/hco/22/GRCh38#25357222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3678208-C-A

25357222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678208-C-T

25357248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3678262-G-A

25357321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3678339-G-A

25357321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3678339-G-C

25357321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3678339-G-T

25357372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3678390-C-T

25357450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3678468-G-A

25357499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3678493-A-G

25357500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3678494-G-A

25357500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3678494-G-C

25357724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3678537-A-G

http://identifiers.org/hco/22/GRCh38#25357846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3678620-A-C

25357846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678620-A-G

http://identifiers.org/hco/22/GRCh38#25357847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3678621-A-C

25357884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678657-G-A

25357884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678657-G-T

25357932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678700-G-A

25357932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678700-G-C

25357932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678700-G-T

25357941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678710-G-A

25357942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678711-G-A

25357942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678711-G-T

25358038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678775-C-G

25358038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678775-C-T

25358135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678881-C-T

25358177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3678925-G-T

25358279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3679015-T-C

25358392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3679133-T-A

25358478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3679216-C-T

25358601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3679341-C-T

25358657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3679399-C-T

25359895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680142-G-A

25359985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680232-G-A

25359985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680232-G-T

25360039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680286-T-C

25360066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680313-A-G

25360066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680313-A-T

25360099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3680346-A-G

http://identifiers.org/hco/22/GRCh38#25360325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680569-C-A

25360325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680569-C-T

25360393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680629-T-C

25360402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680638-G-A

25360402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680638-G-T

http://identifiers.org/hco/22/GRCh38#25360487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680734-C-A

25360552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680804-G-A

25360552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680804-G-T

http://identifiers.org/hco/22/GRCh38#25360571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680819-C-A

25360571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680819-C-T

http://identifiers.org/hco/22/GRCh38#25360634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680836-C-A

25360634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680836-C-G

25360634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680836-C-T

http://identifiers.org/hco/22/GRCh38#25360725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680881-C-A

25360725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680881-C-G

25360725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680881-C-T

http://identifiers.org/hco/22/GRCh38#25360737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3680893-A-C

25360737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680893-A-G

25360844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680994-T-C

25360844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680994-T-G

25360845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680995-T-A

25360845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680995-T-C

25360845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3680995-T-G

http://identifiers.org/hco/22/GRCh38#25360913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3681056-A-C

25360920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681063-G-T

25360949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681082-T-A

25360949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681082-T-C

25361010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681111-T-C

http://identifiers.org/hco/22/GRCh38#25361017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3681119-C-A

25361073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681167-G-T

25361650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681389-G-T

25361789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681517-G-A

25361915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681574-C-T

25361955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681613-T-C

25361983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681640-G-A

25361983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681640-G-T

25361995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681652-A-G

http://identifiers.org/hco/22/GRCh38#25362030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3681686-C-A

25362030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3681686-C-T

http://identifiers.org/hco/22/GRCh38#25362159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3681785-C-A

25364183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3683155-T-C

25364367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3683349-G-T

25364397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3683372-G-A

http://identifiers.org/hco/22/GRCh38#25364552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3684063-C-A

25364724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3684226-G-A

25365147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685046-A-G

25365147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685046-A-T

25365322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685216-A-G

25365381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685269-G-A

25365493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685344-C-T

25365558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3685396-G-A

http://identifiers.org/hco/22/GRCh38#25366105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3692434-C-A

25366627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3692944-C-T

25366986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3693510-C-T

25367032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3693533-C-G

25367032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3693533-C-T

25367290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3693755-C-T

25367306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3693771-C-T

25368957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3695660-T-C

25368978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3695681-C-T

25369120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3695820-T-C

25374289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3697649-G-C

25374367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3697731-G-A

25374578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3697923-T-A

25374592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3697935-C-T

http://identifiers.org/hco/22/GRCh38#25374689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3698011-C-A

25374702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3698024-T-C

25374943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3698257-A-G

25374949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3698261-T-A

25375069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3698387-C-G

25375225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3698562-A-G

25375471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698784-A-G

25375481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698794-A-G

25375489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698802-A-G

25375493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698806-A-G

25375516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698829-T-C

http://identifiers.org/hco/22/GRCh38#25375623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3699084-C-A

25375745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699249-T-A

25375745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699249-T-C

25375745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699249-T-G

http://identifiers.org/hco/22/GRCh38#25375800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3699391-A-C

25375800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699391-A-G

25375963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3699555-T-C

25375963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3699555-T-G

25375975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3699567-G-A

25375975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3699567-G-T

http://identifiers.org/hco/22/GRCh38#25376512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3699833-A-C

25379609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700214-T-A

25379609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700214-T-C

25381250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702024-G-A

25381250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702024-G-T

25381270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702037-G-A

25381270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702037-G-T

http://identifiers.org/hco/22/GRCh38#25381365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3702121-C-A

25381365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702121-C-T

25381374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3702126-T-C

25381374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3702126-T-G

http://identifiers.org/hco/22/GRCh38#25381405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3702157-C-A

25381405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702157-C-T

25381457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702209-G-T

25381482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702234-G-A

25381482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702234-G-T

http://identifiers.org/hco/22/GRCh38#25381491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3702243-C-A

25381491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702243-C-G

25381534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: non coding transcript exon variant
orthologous variants: 3702286-T-C

25381592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3702344-A-G

25381592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3702344-A-T

http://identifiers.org/hco/22/GRCh38#25385634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3715448-C-A

25386012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3716127-A-G

25386669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717043-C-G

25387179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717455-G-C

http://identifiers.org/hco/22/GRCh38#25387328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3717602-A-C

http://identifiers.org/hco/22/GRCh38#25387594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3717871-C-A

25387700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717977-G-C

25387737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718013-A-G

25388166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718533-G-T

25388189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718556-G-A

25388344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718648-T-C

25388617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718869-C-T

25388736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719017-T-C

25388759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719061-G-A

25389227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719453-C-T

http://identifiers.org/hco/22/GRCh38#25389399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3719630-C-A

25389524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719765-A-T

http://identifiers.org/hco/22/GRCh38#25389747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3719923-C-A

25389747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719923-C-T

25389887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720052-T-A

25389887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720052-T-C

25389896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720061-T-A

25390743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721425-T-C

25390783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721464-C-T

25390796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721477-G-A

25395107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3723768-C-T

http://identifiers.org/hco/22/GRCh38#25395445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3724034-C-A

http://identifiers.org/hco/22/GRCh38#25395521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3724116-A-C

25395812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724400-C-T

25396320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724813-T-C

25401069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3731543-T-C

25401349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3731843-C-T

25401367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3731857-T-C

25401443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3731926-T-A

25401443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3731926-T-C

25402987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3734280-G-C

25403323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3734566-T-C

25403380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3734617-A-G

25403392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3734634-C-T

25404027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3735242-T-A

25404027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3735242-T-G

25404031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3735246-G-A

25404034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735249-G-A

25404058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735272-T-C

25404149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735355-A-G

25404439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735652-G-A

http://identifiers.org/hco/22/GRCh38#25404638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3735841-A-C

25404645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735848-G-A

25404774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735985-C-T

25404781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735992-G-C

25404821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3736034-G-T

25405038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3736230-C-T

25405053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3736251-C-T

http://identifiers.org/hco/22/GRCh38#25405096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#3736298-C-A

25405096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3736298-C-T