90471761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81877375-T-A

90471986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron variant
orthologous variants: 81877198-G-A

90472419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron variant
orthologous variants: 81875304-T-A

90472429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron variant
orthologous variants: 81875294-C-G

90472503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81875213-C-T

90472618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81875170-T-C

http://identifiers.org/hco/5/GRCh38#90472753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81875060-C-A

90472861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81874969-G-A

90472881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81874950-G-T

90472987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860848-A-G

90473320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860560-A-G

http://identifiers.org/hco/5/GRCh38#90473379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81860505-A-C

90473379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860505-A-G

90473379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860505-A-T

90473423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860462-C-T

http://identifiers.org/hco/5/GRCh38#90473433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81860456-C-A

90473433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860456-C-T

90473494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860398-G-A

90473510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860382-T-C

90473557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860339-G-C

90473557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860339-G-T

90473630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 81860289-C-T

90473696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81860222-G-T

http://identifiers.org/hco/5/GRCh38#90473731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81860188-C-A

http://identifiers.org/hco/5/GRCh38#90473752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81860177-C-A

90473752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: 81860177-C-T

90473816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81860121-G-A

90473816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81860121-G-C

90473816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81860121-G-T

90473844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: 81860094-T-A

90473844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: 81860094-T-C

90473844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, missense_variant
orthologous variants: 81860094-T-G

http://identifiers.org/hco/5/GRCh38#90473909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81860029-C-A

90473909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 81860029-C-T

90473979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859959-G-A

90473979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859959-G-C

90473979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859959-G-T

90473982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859956-T-C

90473982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859956-T-G

90474105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 81859833-A-T

http://identifiers.org/hco/5/GRCh38#90474111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859827-C-A

90474111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 81859827-C-T

90474149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 81859789-C-G

90474149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 81859789-C-T

90474318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 81859617-G-A

90474318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 81859617-G-T

http://identifiers.org/hco/5/GRCh38#90474345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859600-C-A

90474484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859458-G-C

90474503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859440-T-G

90474521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859424-A-G

http://identifiers.org/hco/5/GRCh38#90474523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859422-C-A

90474523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859422-C-T

90474526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859419-A-T

90474604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859362-G-A

90474604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859362-G-C

90474604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859362-G-T

90474668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859303-A-G

90474668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859303-A-T

90474717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859249-T-A

90474717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859249-T-C

90474717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859249-T-G

http://identifiers.org/hco/5/GRCh38#90474733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859232-C-A

90474733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859232-C-T

http://identifiers.org/hco/5/GRCh38#90474737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859228-C-A

90474737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859228-C-G

90474737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859228-C-T

90474740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859225-G-A

90474740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859225-G-C

90474759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859208-T-C

90474759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859208-T-G

http://identifiers.org/hco/5/GRCh38#90474762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859205-C-A

90474762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 81859205-C-T

90474830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: intron variant
orthologous variants: 81859140-C-T

http://identifiers.org/hco/5/GRCh38#90474874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859104-C-A

90474892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859086-T-G

90474895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859083-G-C

90474895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859083-G-T

90474928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859050-G-A

90474928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859050-G-T

http://identifiers.org/hco/5/GRCh38#90474930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81859048-C-A

90474930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859048-C-G

90474987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859007-G-T

90474994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859001-G-A

90474994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859001-G-C

90475046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858951-T-C

90475099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858897-G-T

http://identifiers.org/hco/5/GRCh38#90475129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81858864-C-A

90475129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858864-C-T

90475427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858574-T-C

90475464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858542-C-G

90475591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858457-C-T

90476374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858002-T-C

90476604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857824-C-T

http://identifiers.org/hco/5/GRCh38#90476782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81857707-C-A

90476794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857695-C-G

90476815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857674-G-A

90477021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857471-T-C

90477024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857468-G-T

90477385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81857335-A-G

90477484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857243-G-A

90477638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857093-T-A

90478061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857062-T-G

90478108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857020-C-T

90478276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856851-T-A

90478320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856802-C-T

90480691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855108-C-T

90480845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854960-G-A

90481058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854759-G-T

90481419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854264-A-T

90481717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853979-G-A

http://identifiers.org/hco/5/GRCh38#90481743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81853954-A-C

90481957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852671-C-T

90482054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852568-A-G

90483853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852212-G-C

90483902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852168-A-G

90483913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852158-G-A

90484039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852049-A-G

90484342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81851737-T-C

90484367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81851712-C-T

90484433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81851663-G-T

90484527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81851584-A-T

90484742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81851391-A-G

90485553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81847992-G-A

90485553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81847992-G-T

90485592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81847953-C-T

90485691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 81847854-A-G

90485735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847812-A-G

http://identifiers.org/hco/5/GRCh38#90485749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81847798-C-A

90485749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847798-C-T

http://identifiers.org/hco/5/GRCh38#90485783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81847758-C-A

90485783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847758-C-G

90485783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847758-C-T

90485786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847755-G-A

90485786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847755-G-C

90485786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847755-G-T

90485813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847734-T-C

90485813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847734-T-G

90486366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844338-A-G

90486377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844330-A-G

90486392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844318-A-G

http://identifiers.org/hco/5/GRCh38#90487377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81843479-A-C

90487377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843479-A-T

http://identifiers.org/hco/5/GRCh38#90487889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81843003-C-A

90487900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842992-T-C

90487927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842965-T-A

90487969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842923-G-C

90487969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842923-G-T

90487981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842913-T-A

90487985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842909-T-C

90487988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842906-T-C

90488070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81842824-A-G

90488177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842709-A-G

90488178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842708-A-G

90488223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842672-T-A

90488223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842672-T-C

90488242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842668-T-C

90488259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842651-G-T

90488280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842638-G-A

90489093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81842006-A-G

90489150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81841962-C-T

90489163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81841955-G-T

90489190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81841932-T-C

90496507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81836884-T-C

90496706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81836680-C-G

90496815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81836567-T-C

90497037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81836195-A-G

90497574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835369-G-A

90497739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835211-G-A

90497746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835204-G-A

90497746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835204-G-T

90498538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835116-T-G

90498552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835102-C-T

90498553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81835101-A-T

90500464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81832965-G-A

90500548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81832886-T-C

90500747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81831326-T-C

http://identifiers.org/hco/5/GRCh38#90500888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81831194-A-C

90500976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81831115-C-G

90501075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81831017-A-T

90501449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830922-G-A

90501518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830856-C-T

90502033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830203-A-G

90502038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830198-C-G

http://identifiers.org/hco/5/GRCh38#90502114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81830137-C-A

90502138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830121-G-A

90502138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81830121-G-T

90502382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829836-T-G

90502429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829791-T-C

90502799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829307-T-A

90502832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829286-A-T

90502855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829265-A-T

90502865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829258-A-G

90503342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829090-T-G

90503382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829049-T-C

90503382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829049-T-G

90503395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829036-A-G

90503415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81829018-T-C

90503732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828760-A-G

90503745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828746-C-T

90503997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828557-G-A

90504047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828507-T-G

90504077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828479-A-G

90504171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828384-A-G

90504685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828175-C-T

90504758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828113-A-G

90504770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828096-T-A

90504792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828074-T-C

90504795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828071-G-A

90504795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81828071-G-T

90504890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81827959-A-T

90505071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81827446-A-T

90505144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81827388-T-G

90505230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81827306-G-A

90505353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81827026-G-T

90505702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81826717-G-A

90506184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81826534-G-A

90506278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81826503-G-C

90506537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826367-A-G

90506543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826361-G-A

90506543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826361-G-C

90506612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826295-G-A

90506633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826274-G-T

90506663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81826244-G-A

90506663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 81826244-G-T

http://identifiers.org/hco/5/GRCh38#90506684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81826223-C-A

90510713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825621-A-G

90510714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825620-G-A

90510721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825613-G-C

90510738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825596-T-C

90510739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825595-G-A

90510812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825537-T-G

90510831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825518-A-G

90510864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825515-G-A

http://identifiers.org/hco/5/GRCh38#90510882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81825497-A-C

90510882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825497-A-T

90510957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825445-T-C

90511103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825260-A-G

90511104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825259-C-T

90511256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81825075-A-T

90511590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824720-C-T

90511640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824700-G-T

90511667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824677-T-C

90511744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824601-G-T

90511746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824599-G-A

90511813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824532-G-A

90511948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824407-G-T

90511966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824394-A-T

90512016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81824304-T-A

http://identifiers.org/hco/5/GRCh38#90512028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81824292-C-A

90512056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81824236-A-G

90512074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81824218-T-C

90512083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81824209-G-A

90512083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81824209-G-C

90512083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81824209-G-T

90512143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81824149-T-A

90512143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81824149-T-C

90512190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81824107-G-A

http://identifiers.org/hco/5/GRCh38#90512221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81824087-A-C

http://identifiers.org/hco/5/GRCh38#90512370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81823958-C-A

90512370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823958-C-T

90512411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823921-T-C

http://identifiers.org/hco/5/GRCh38#90512424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81823905-C-A

90512424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823905-C-T

90512464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823869-T-C

90512489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823843-A-G

http://identifiers.org/hco/5/GRCh38#90512496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81823836-C-A

90512533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823815-T-C

90512573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823779-A-G

90512573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823779-A-T

90512599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823744-A-G

90512602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823741-G-T

90512726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823639-T-C

90512892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823452-T-C

90513019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823322-T-G

90513032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823308-A-G

90513082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823262-G-T

90513124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823218-G-T

90513214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823128-A-T

90513318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81823019-T-C

http://identifiers.org/hco/5/GRCh38#90513456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81822868-C-A

90513987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81822374-A-G

90514000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81822361-T-C

90514035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81822332-A-G

http://identifiers.org/hco/5/GRCh38#90514049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81822320-C-A

90514112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81822263-T-C

90514254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3 prime UTR variant
orthologous variants: 81822115-G-C

90514254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3 prime UTR variant
orthologous variants: 81822115-G-T

http://identifiers.org/hco/5/GRCh38#90514382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#81821989-C-A

90514457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30075
most severe consequence: 3 prime UTR variant
orthologous variants: 81821929-A-G