30938697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55335598-A-G

30938703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55335604-G-T

http://identifiers.org/hco/7/GRCh38#30938740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55335651-C-A

30938740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: 55335651-C-T

30938743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: 55335654-T-C

30938753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: 55335664-C-G

30938829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: 55335729-G-A

30938829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: 55335729-G-T

http://identifiers.org/hco/7/GRCh38#30938863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55335753-C-A

30938863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55335753-C-T

30938920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55335817-G-A

30938920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55335817-G-T

http://identifiers.org/hco/7/GRCh38#30938984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55335885-A-C

30938984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55335885-A-G

30938991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55335891-G-T

30939029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55335936-G-T

30939192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336075-C-G

http://identifiers.org/hco/7/GRCh38#30939330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55336229-A-C

30939331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336230-T-C

30939561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336412-G-A

30939587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336436-A-G

30939620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336468-T-C

30939754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336600-G-A

30939798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336627-C-T

30939990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336806-G-A

30940062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55336862-T-C

30940715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337416-G-C

30940729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337418-A-T

http://identifiers.org/hco/7/GRCh38#30940810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55337497-C-A

30940810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337497-C-T

30940844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55337528-G-A

http://identifiers.org/hco/7/GRCh38#30941665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55338001-C-A

30941752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338105-C-T

30941768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338121-C-T

http://identifiers.org/hco/7/GRCh38#30941776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55338129-C-A

30942393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338580-C-T

30942428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338614-T-G

30942567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338751-A-G

30942567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55338751-A-T

30961096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350739-G-T

30961204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350836-G-A

30961230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350864-A-G

30961230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55350864-A-T

30961441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351064-A-T

30961536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351138-A-G

http://identifiers.org/hco/7/GRCh38#30962305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55351770-A-C

30962419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351872-G-A

30962545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351986-G-A

30962545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55351986-G-T

30962597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352010-T-C

30962600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352013-C-T

30962626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352043-C-G

30962626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352043-C-T

30962938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352246-T-C

30963329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352596-C-T

30963383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352669-A-G

30963443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352779-A-G

30963528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352855-A-G

30963531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352858-A-G

30963553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55352872-A-T

30963686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353015-G-A

30963686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353015-G-C

30963847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353186-G-C

http://identifiers.org/hco/7/GRCh38#30963895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55353228-C-A

30963895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353228-C-G

30963896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353229-T-C

30963940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353270-T-C

http://identifiers.org/hco/7/GRCh38#30963945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55353275-A-C

30963949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353279-A-G

30963949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55353279-A-T

30964049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55353359-G-A

http://identifiers.org/hco/7/GRCh38#30964095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55353396-C-A

30964095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55353396-C-G

30964095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55353396-C-T

30964107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55353408-G-A

30964107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55353408-G-C

30964107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55353408-G-T

30964108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55353409-T-C

30964108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55353409-T-G

http://identifiers.org/hco/7/GRCh38#30964120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55353421-C-A

30964120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55353421-C-T

30967346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354656-T-C

30967365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354674-G-A

30967365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354674-G-T

http://identifiers.org/hco/7/GRCh38#30967622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55354880-C-A

30967670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55354928-C-T

30967773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355018-C-G

30967782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355027-A-G

30968489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355547-T-C

30968593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355575-T-C

http://identifiers.org/hco/7/GRCh38#30968614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55355596-C-A

30968614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355596-C-T

30968640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355622-C-T

30968723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355750-T-G

30968727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355754-G-T

http://identifiers.org/hco/7/GRCh38#30968742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55355769-C-A

30968781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355812-G-A

30968781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55355812-G-T

http://identifiers.org/hco/7/GRCh38#30968908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55355935-A-C

30968927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: missense variant
orthologous variants: 55355954-A-G

30968969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55355986-C-T

30968982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55355999-A-G

30968999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356016-C-T

http://identifiers.org/hco/7/GRCh38#30969041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55356047-C-A

30969041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356047-C-T

30969103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: synonymous variant
orthologous variants: 55356109-G-A

30969103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: synonymous variant
orthologous variants: 55356109-G-T

30969198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356204-A-G

30969199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356205-A-T

30969207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356213-T-G

30969245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356244-G-A

30969245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356244-G-T

http://identifiers.org/hco/7/GRCh38#30969305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55356291-A-C

30969305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356291-A-G

30969346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356307-G-T

30969405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356349-G-T

30969515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356392-G-A

30969515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron variant
orthologous variants: 55356392-G-T

30969557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 55356443-G-T

http://identifiers.org/hco/7/GRCh38#30969635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55356517-A-C

30969816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 55356623-T-C

30969816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 55356623-T-G

30969827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 55356633-G-C

30969854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 55356661-G-A

30969869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 55356675-G-A

30969869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 55356675-G-C

30969869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 55356675-G-T

30969972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 55356788-T-G

30970025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55356816-A-T

30970048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55356826-C-G

30970049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55356827-T-C

30970049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55356827-T-G

http://identifiers.org/hco/7/GRCh38#30970092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55356866-A-C

30970249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55357023-G-A

30970799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55357519-T-C

30970884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 55357607-G-T

30971022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357670-G-A

30971022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357670-G-T

30971030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357678-G-T

30971031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357679-G-A

30971031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357679-G-C

30971031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55357679-G-T

http://identifiers.org/hco/7/GRCh38#30971111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55357729-C-A

30971111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 55357729-C-T

http://identifiers.org/hco/7/GRCh38#30971154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55357772-C-A

30971154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55357772-C-T

http://identifiers.org/hco/7/GRCh38#30971187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55357805-C-A

30971187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55357805-C-T

30971224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55357842-A-G

30971224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55357842-A-T

30971231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357849-T-A

30971231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357849-T-C

30971322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357939-G-A

30971354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357971-T-A

30971354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357971-T-G

http://identifiers.org/hco/7/GRCh38#30971364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55357988-A-C

30971364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357988-A-G

30971364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55357988-A-T

http://identifiers.org/hco/7/GRCh38#30971485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55358122-C-A

30971581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358293-C-T

30971846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358563-T-A

30971846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358563-T-G

http://identifiers.org/hco/7/GRCh38#30971914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55358642-C-A

30971914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358642-C-T

30972137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55358865-A-G

30972137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55358865-A-T

30972186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358900-C-T

30972270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358961-G-A

30972270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55358961-G-T

30972533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55359207-G-T

30972566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55359238-C-T

30973528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55359690-T-C

30973602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55359758-G-A

30973753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360018-A-G

30973907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360163-T-C

30973946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360201-G-T

30973947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360216-G-A

30973947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360216-G-T

30973982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55360250-C-T

30974128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55360396-C-T

http://identifiers.org/hco/7/GRCh38#30974191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55360459-C-A

30974191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360459-C-T

http://identifiers.org/hco/7/GRCh38#30974336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55360595-C-A

http://identifiers.org/hco/7/GRCh38#30974339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55360598-C-A

30974339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360598-C-T

http://identifiers.org/hco/7/GRCh38#30974513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55360767-C-A

30974846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55360947-G-T

30974894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55360994-A-G

30974908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361008-G-T

http://identifiers.org/hco/7/GRCh38#30975095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361225-C-A

30975095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361225-C-G

30975095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361225-C-T

30975176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361295-T-G

30975384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361413-C-T

30975390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361419-C-T

http://identifiers.org/hco/7/GRCh38#30975657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361605-C-A

30975657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361605-C-T

http://identifiers.org/hco/7/GRCh38#30975704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361642-C-A

30975704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361642-C-G

30975711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361649-T-C

http://identifiers.org/hco/7/GRCh38#30975730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361673-C-A

http://identifiers.org/hco/7/GRCh38#30975733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361676-C-A

30975733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361676-C-T

http://identifiers.org/hco/7/GRCh38#30975742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55361683-C-A

30975742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361683-C-G

30975742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361683-C-T

30975768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55361708-T-C

30975779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 55361719-G-A

30975779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained, synonymous_variant
orthologous variants: 55361719-G-T

30975884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55361869-G-A

30975888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55361873-G-A

30976094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55362128-G-T

30976225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55362249-G-T

30976945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363011-C-T

30976959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363025-T-C

30976965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363031-C-T

30976969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363035-C-T

30977325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363843-G-A

30977325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363843-G-C

30977331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363849-T-C

30977331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363849-T-G

30977336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363854-G-A

http://identifiers.org/hco/7/GRCh38#30977378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55363888-C-A

30977378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363888-C-T

30977398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55363908-T-G

http://identifiers.org/hco/7/GRCh38#30977414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55363924-C-A

30977560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364048-G-C

30977798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364210-G-A

30977839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364247-A-T

30978211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364608-T-C

30978696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364847-A-G

30978697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364848-C-T

http://identifiers.org/hco/7/GRCh38#30978827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55364919-A-C

30978827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55364919-A-G

30978984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365023-G-A

30978984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365023-G-T

30978985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365024-T-C

http://identifiers.org/hco/7/GRCh38#30978989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55365028-C-A

30978989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365028-C-T

30979036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365071-T-C

30979037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55365072-C-G

30979139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55365174-G-C

30979160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55365195-T-G

30979315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365339-G-A

30979315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365339-G-T

http://identifiers.org/hco/7/GRCh38#30979371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55365363-C-A

30979386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365378-T-A

30979386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365378-T-C

http://identifiers.org/hco/7/GRCh38#30979387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55365379-C-A

30979387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365379-C-T

30979414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365403-T-A

30979414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365403-T-C

30979415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365404-G-A

30979415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365404-G-C

30979415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365404-G-T

30979489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55365474-T-G

30979569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55365549-A-G

30979719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55365694-T-A

30979886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55365840-T-G

30980430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366044-A-G

30980431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366045-T-C

30980445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366059-G-A

30980602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366194-C-T

30980711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366291-G-A

30980795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366750-A-G

30980902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55366843-A-G

30981508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55367584-A-G

30981859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55367928-G-A

http://identifiers.org/hco/7/GRCh38#30983427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369235-C-A

30983427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55369235-C-T

http://identifiers.org/hco/7/GRCh38#30983442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369249-C-A

30983442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369249-C-G

30983451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369258-T-C

30983463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369270-C-T

http://identifiers.org/hco/7/GRCh38#30983580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369372-C-A

30983580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55369372-C-G

30983580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55369372-C-T

30983670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369456-G-A

30983670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369456-G-T

30983673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369459-G-A

30983673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369459-G-C

30983673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369459-G-T

30983684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369470-T-A

30983684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369470-T-C

30983684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369470-T-G

30983689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369475-A-G

http://identifiers.org/hco/7/GRCh38#30983698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369484-C-A

30983698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369484-C-G

http://identifiers.org/hco/7/GRCh38#30983710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369495-C-A

30983710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55369495-C-T

http://identifiers.org/hco/7/GRCh38#30983712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369497-C-A

http://identifiers.org/hco/7/GRCh38#30983733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369556-C-A

30983733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369556-C-T

30983742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369565-A-G

30983742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369565-A-T

30983748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55369571-A-G

30983860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55369670-C-T

30983873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55369683-C-G

http://identifiers.org/hco/7/GRCh38#30983985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#55369779-C-A

30984021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55369847-T-G

30984083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55369926-C-G

30984083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55369926-C-T

30984203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55370048-C-G

30984203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55370048-C-T

30984225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55370075-G-A

30984225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55370075-G-T

30984306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55370127-A-G

30984358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 55370178-A-G

30986599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55371750-A-T

30986749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55371863-C-T

30986828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55371935-G-A

30986858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55371964-C-G

30986933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55372058-G-A

30987124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55372273-T-C

30987993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373016-G-A

30988044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373051-G-C

http://identifiers.org/hco/7/GRCh38#30988387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55373345-A-C

30988460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373421-A-G

30988647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373571-C-G

30988647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373571-C-T

30988785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373728-G-T

30988786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373729-C-G

30988786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373729-C-T

30988787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55373730-G-A

http://identifiers.org/hco/7/GRCh38#30992176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55375554-C-A

30992321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55375685-A-G

30992354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55375720-G-A

30992410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55375785-T-C

30992415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55375790-C-T

30992456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55375829-C-G

30992661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376082-C-T

30993070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376539-G-A

30993070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376539-G-T

http://identifiers.org/hco/7/GRCh38#30993124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55376591-C-A

30993124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376591-C-G

30993124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376591-C-T

30993130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376597-A-G

30993154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55376611-G-T

30993169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55376626-A-G

http://identifiers.org/hco/7/GRCh38#30993170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55376627-C-A

30993170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55376627-C-G

http://identifiers.org/hco/7/GRCh38#30993215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4266
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#55376679-C-A