183099260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5 prime UTR variant
orthologous variants: 48443421-T-C

183099260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5 prime UTR variant
orthologous variants: 48443421-T-G

http://identifiers.org/hco/4/GRCh38#183099277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#48443404-A-C

183099277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48443404-A-G

183099297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48443384-T-A

183099297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 48443384-T-G

183099359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 48443324-C-T

http://identifiers.org/hco/4/GRCh38#183099360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#48443323-C-A

183099360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 48443323-C-G

183099360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 48443323-C-T

183099691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48443016-G-A

183099691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48443016-G-C

183099816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48442881-A-G

183100065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48442595-G-C

183100155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48442501-C-T

183100345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48442333-C-G

183100345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48442333-C-T

183100452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48442049-A-G

183100890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48441408-T-A

183101413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48440922-A-G

183101592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48440747-T-A

183101753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48440594-C-T

183102002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48440332-G-A

183102876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48439733-T-C

183103058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48439603-A-G

183103205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48439468-G-A

183104275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48439248-A-G

http://identifiers.org/hco/4/GRCh38#183104593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48438899-A-C

183104614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48438878-C-T

183104686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48438830-C-G

183104700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48438815-T-G

183107776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48436607-T-A

183108018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48436377-A-G

183108098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48436298-A-G

183108123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48436273-A-T

183108157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48436246-C-T

183110027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48434891-A-G

183110029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48434889-T-G

183110118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48434808-C-G

183110159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48434779-G-T

183111331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48431618-G-A

183111387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48431560-A-G

183111455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48431500-T-G

183112742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48430455-T-C

183116591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48428369-C-G

183116591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48428369-C-T

183118408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48427665-G-T

183118420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48427653-G-A

183118838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48427249-G-A

183118976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48427136-T-G

183118986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48427134-C-G

183119412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48425778-C-T

183119487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48425730-T-C

183119552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48425695-C-T

183120113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48425318-T-C

183125628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418185-A-G

183125628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418185-A-T

183125652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418163-T-A

183125652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418163-T-C

183125695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418120-C-T

183125758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418076-C-T

183125792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48418045-T-C

183129097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416460-T-C

183129297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416292-T-C

183129458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416135-T-C

183129464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416129-A-G

183129479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416110-C-G

183129521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416075-G-C

183129524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416072-C-T

183129606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48416017-T-C

http://identifiers.org/hco/4/GRCh38#183129759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48415870-A-C

183129759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415870-A-G

183129907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415723-G-C

183129944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415690-G-A

http://identifiers.org/hco/4/GRCh38#183130567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48415374-A-C

183130657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415285-G-T

183130734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415219-A-G

183130734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48415219-A-T

183137968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48406206-T-A

183138034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48406143-A-G

183138109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48406069-C-T

183138895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48405248-C-G

183138976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48405182-C-T

183139056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48405119-A-G

183139065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48405110-A-G

183139462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48404943-T-A

183141612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403804-T-A

183141612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403804-T-C

183141613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403803-C-G

183141720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403713-T-C

183141736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403698-A-G

183142042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403441-A-G

183142100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403384-C-T

183142141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403360-C-T

183142188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403334-T-G

183142528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48403064-T-C

183142598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48402984-A-G

183142830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48402775-G-A

http://identifiers.org/hco/4/GRCh38#183142987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48402403-C-A

183143390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48402032-C-T

183143788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48401853-A-G

183144025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48401718-A-G

183144513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48401275-C-T

183144516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48401272-T-C

183144837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48400972-C-T

183144993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48400818-G-A

183145219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48400627-G-T

183147449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48399297-G-C

183147562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48399198-A-G

183147562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48399198-A-T

183147717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48399090-G-T

183147822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48399031-G-C

183148103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48398779-C-G

183148113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48398769-G-A

183148193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48398691-G-A

183148562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48398271-T-C

183154705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48397807-A-G

183154718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48397794-C-T

183154765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48397760-G-C

183154819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48397707-C-T

183154957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48397590-C-T

183154991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48397559-G-A

183155320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48397242-A-T

183155458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48397133-G-A

http://identifiers.org/hco/4/GRCh38#183155560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48397072-C-A

183155560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48397072-C-T

183155977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48396703-A-G

183164258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48394625-G-T

183164263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48394620-C-T

183164570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48394437-A-G

183164603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48394404-A-G

183164997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48394042-A-T

http://identifiers.org/hco/4/GRCh38#183165083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48393966-A-C

183165122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48393929-T-C

183165364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48393686-G-T

183165952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48393139-G-T

183166134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48392956-T-A

183166241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48392857-A-G

183167101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48391968-A-G

183167103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48391966-A-G

183167492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48391315-G-C

183167750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48391084-G-A

183167789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48391045-T-C

183168444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48390725-A-G

183168471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48390700-A-T

183168594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48390614-T-C

183168617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48390591-A-G

183168820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48390316-A-G

183169858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389836-A-G

183170031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389668-A-G

183170219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389495-A-T

183170233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389481-A-G

183170237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389477-G-T

183170282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48389419-G-A

183171694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48388131-C-G

183171744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48388090-A-G

183175787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48385953-G-A

183175852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48385878-C-T

183175894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48385829-G-A

183175944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48385784-C-T

http://identifiers.org/hco/4/GRCh38#183177193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48385101-A-C

183177273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48385039-T-G

183177577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384753-A-G

183177720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384595-C-T

183177729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384586-A-G

183177736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384581-A-G

183177767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384514-G-A

183177930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384360-T-G

183178937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384056-G-A

183178937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384056-G-T

183178975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48384019-G-A

183179411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383532-T-A

183179552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383455-C-T

183179553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383454-C-T

183179573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383429-G-C

183179602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383400-G-C

183179694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383309-G-T

183179709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383292-T-C

183179927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383104-A-G

183179950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48383080-A-T

http://identifiers.org/hco/4/GRCh38#183180081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48382969-A-C

183180202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48382887-G-A

183180284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48382824-A-G

http://identifiers.org/hco/4/GRCh38#183180332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48382771-C-A

183181939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48378757-G-A

183182071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48378630-A-G

183182334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48378309-C-T

183182368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48378242-G-A

183182817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48377870-A-G

183184036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48377020-C-T

183184111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376944-C-T

183184169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376885-A-G

183184266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376785-T-C

183184301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376755-A-G

183184312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376746-A-G

183186259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376719-T-G

183186319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376663-T-C

183186380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376598-A-G

183186394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376586-G-A

183186394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376586-G-T

183186522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376512-G-A

http://identifiers.org/hco/4/GRCh38#183190603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48376263-A-C

183190752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48376111-A-G

183191071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48375828-T-C

183191431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48375463-T-C

183193543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373785-G-A

183193543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373785-G-T

http://identifiers.org/hco/4/GRCh38#183194128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48373278-C-A

http://identifiers.org/hco/4/GRCh38#183194176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48373231-A-C

183194212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373191-C-T

183194258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373149-A-G

183194271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373142-G-T

183194282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373136-G-A

183194283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373135-G-A

183194302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48373116-G-A

183194575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48372393-G-T

183194673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48372326-T-C

183195067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48371425-G-T

183195160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48371298-T-A

http://identifiers.org/hco/4/GRCh38#183195251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48371216-C-A

183195259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48371208-A-T

183196332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48370495-G-C

183196682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48370140-T-C

183196794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48370071-C-G

183196860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48370011-G-A

183196860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48370011-G-T

183196938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48369943-A-G

183197017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48369834-G-A

183197294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48369549-A-G

183197587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48369258-G-A

183197605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48369240-G-T

183197961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48368706-T-C

183199067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358670-G-A

183199211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358526-G-A

183199269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358477-G-A

183199269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358477-G-T

183199430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358337-A-G

183199617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48358191-G-A

183200497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48357388-A-T

183200538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48357348-T-G

183200704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48357205-A-G

183200713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48357196-C-T

183200744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48357165-C-T

183201441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48356619-C-T

183206777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48354754-G-A

183207588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48354265-G-A

183207594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48354259-T-C

183207820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48354018-A-G

http://identifiers.org/hco/4/GRCh38#183207831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48354004-C-A

183207831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48354004-C-T

183207845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353991-A-T

http://identifiers.org/hco/4/GRCh38#183207871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353965-A-C

183207871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353965-A-T

http://identifiers.org/hco/4/GRCh38#183207878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353958-C-A

183207878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353958-C-G

183207878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353958-C-T

http://identifiers.org/hco/4/GRCh38#183207882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353955-C-A

183207882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353955-C-T

http://identifiers.org/hco/4/GRCh38#183207886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353951-C-A

183207895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353945-A-T

http://identifiers.org/hco/4/GRCh38#183207898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353942-C-A

183207898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353942-C-T

http://identifiers.org/hco/4/GRCh38#183207899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353941-A-C

http://identifiers.org/hco/4/GRCh38#183207910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48353930-C-A

183207991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48353851-G-A

183207991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48353851-G-T

183207992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48353850-G-A

183207992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48353850-G-C

183208024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48353818-T-G

183208193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353657-A-G

183208324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353533-C-T

183208353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353506-G-A

183208582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48353196-G-T

183208714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352927-G-A

http://identifiers.org/hco/4/GRCh38#183209016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48352478-A-C

183209016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 48352478-A-G

183209044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352450-T-A

http://identifiers.org/hco/4/GRCh38#183209049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48352445-C-A

183209050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352444-T-C

183209063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352432-A-G

183209063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352432-A-T

http://identifiers.org/hco/4/GRCh38#183209117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48352376-A-C

183209117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352376-A-G

183209169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352328-T-C

183209169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48352328-T-G

183210941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48351377-C-T

183211437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350903-G-A

183211462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350878-A-G

183211641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350711-A-G

183211789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350587-T-C

183211828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350556-T-A

183212084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350403-G-T

183212145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350395-C-T

183212413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350224-C-T

183212602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48350063-T-C

183212771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349917-G-A

183212934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349790-G-A

183212948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349777-G-A

183212952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349773-C-T

183213106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349664-C-T

183213122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349652-G-T

183213131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349643-G-A

183213211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349573-G-C

183213237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349547-A-G

183213310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48349493-T-A

183231908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346562-A-G

183232015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346453-G-A

183232089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346373-G-A

183232352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346127-A-G

183232396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346102-T-C

http://identifiers.org/hco/4/GRCh38#183232433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48346065-C-A

183232433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48346065-C-G

183233532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48345189-G-A

183233557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48345164-G-A

http://identifiers.org/hco/4/GRCh38#183233663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48345079-C-A

http://identifiers.org/hco/4/GRCh38#183233673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48345068-C-A

183233850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48344933-G-A

http://identifiers.org/hco/4/GRCh38#183234087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48344726-C-A

183234185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344633-C-T

183234186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344632-C-T

183234194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344629-A-G

http://identifiers.org/hco/4/GRCh38#183234371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48344439-A-C

183234406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344408-C-G

183234486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344319-G-A

183234644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48344227-G-C

183235404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48343540-A-G

183235655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48343286-T-C

183235687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48343249-A-G

183237331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342919-C-T

183237463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342803-C-T

183237658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342659-T-C

183237931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342454-C-G

183238058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342381-A-G

183238380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342103-T-A

183238446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48342048-C-G

http://identifiers.org/hco/4/GRCh38#183239422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48341046-A-C

http://identifiers.org/hco/4/GRCh38#183239486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48340982-C-A

183240147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48340220-G-A

http://identifiers.org/hco/4/GRCh38#183240252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48340115-A-C

183240252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 48340115-A-G

183240547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339837-G-A

183240547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339837-G-T

183240570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339815-G-A

183240570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339815-G-T

183240630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339780-A-G

183240630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339780-A-T

http://identifiers.org/hco/4/GRCh38#183240633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48339777-C-A

183240633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48339777-C-G

http://identifiers.org/hco/4/GRCh38#183240683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48339766-C-A

183240683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48339766-C-T

183240720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48339729-G-T

183240845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48339610-C-T

183241023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48339489-C-G

183241023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48339489-C-T

183242350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48339008-C-T

183242712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48338698-A-G

183242729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48338681-A-G

http://identifiers.org/hco/4/GRCh38#183242760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48338637-C-A

183242823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48338570-A-G

http://identifiers.org/hco/4/GRCh38#183242956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48338474-C-A

183243300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48338219-C-G

183243300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48338219-C-T

183243650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48337917-T-G

183244665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48337049-A-G

183244703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48337011-T-C

183244708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48337006-C-T

183244847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336902-T-C

http://identifiers.org/hco/4/GRCh38#183245394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48336678-C-A

183245394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336678-C-T

183245399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336673-T-C

183245399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336673-T-G

183245443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48336629-G-T

183245628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336500-C-T

183245629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336499-A-G

183245632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336497-G-A

183245633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336496-T-C

183245695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336447-G-A

183245695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336447-G-T

183245705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336437-T-C

183245805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48336349-C-T

http://identifiers.org/hco/4/GRCh38#183245842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48336319-C-A

http://identifiers.org/hco/4/GRCh38#183246317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48335933-C-A

183246407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48335844-A-G

183247027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48335233-T-C

183247851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48334625-T-C

183247860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48334616-C-T

183247993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48334496-A-G

183248025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48334466-C-T

183248610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48333374-T-A

http://identifiers.org/hco/4/GRCh38#183248666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48333320-C-A

183248666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48333320-C-T

183248879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48333115-A-G

183248942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332976-G-C

183248942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332976-G-T

183248945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332973-G-A

183248945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332973-G-T

183249011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332881-A-G

183249201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332743-G-A

183249354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332402-C-G

183249726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332097-G-A

183249795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332057-T-C

183249795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332057-T-G

183249823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332029-T-C

183249823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48332029-T-G

183250017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331840-T-A

http://identifiers.org/hco/4/GRCh38#183250026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48331834-C-A

183250026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331834-C-T

http://identifiers.org/hco/4/GRCh38#183250086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48331702-C-A

183250086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331702-C-T

183250120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331665-A-G

183250179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331463-C-G

183250232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331391-C-T

183250312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331320-T-C

183250463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331195-A-G

183250474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331186-G-A

183250553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331116-T-C

183250665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48331045-T-C

183250767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330950-G-A

183251049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330652-C-T

http://identifiers.org/hco/4/GRCh38#183251254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48330424-C-A

183251254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330424-C-T

183251265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330413-C-G

183251318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330328-C-T

183251369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330276-T-G

183251525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330154-C-G

183251525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330154-C-T

183251565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48330116-A-G

183251955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329737-A-G

183252001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329691-G-T

183252056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329642-C-T

183252124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329569-A-G

183252129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329564-A-G

183252404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329301-C-G

183252494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329221-G-A

183252631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48329109-A-G

183253886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48328375-C-T

183253974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48328287-A-G

183254076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48328190-T-G

183254446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48327822-C-G

183254446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48327822-C-T

183256012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48326404-C-T

183256147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48326272-T-G

183256373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48326086-A-G

http://identifiers.org/hco/4/GRCh38#183256412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48326036-C-A

183256558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48325923-A-G

183256592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48325891-G-C

183256708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48325790-A-G

183256955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48325591-G-A

183256983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48325563-G-A

183257336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48325245-T-C

183257519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48325079-A-G

183257869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48324801-A-G

183258095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48324523-A-G

183258370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48324297-G-A

http://identifiers.org/hco/4/GRCh38#183259564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48322987-C-A

183259564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48322987-C-T

183259630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48322910-T-C

183260346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48322297-T-C

http://identifiers.org/hco/4/GRCh38#183260842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48321892-C-A

183260853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321881-G-A

183260926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48321808-C-T

183260950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321784-C-G

183260950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48321784-C-T

183261112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321622-A-G

183261172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321562-C-T

183261220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321514-A-G

183261221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321513-C-T

183261307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321427-T-G

183261368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48321369-C-G

http://identifiers.org/hco/4/GRCh38#183261371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48321366-C-A

183261491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48321246-T-C

183261491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48321246-T-G

183261493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48321244-A-T

183261496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48321241-G-C

183261496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 48321241-G-T

183261594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321151-G-A

183261594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321151-G-T

183261625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321118-A-G

183261654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321107-T-A

183261654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321107-T-C

183261654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48321107-T-G

http://identifiers.org/hco/4/GRCh38#183261704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48321059-C-A

183261742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48320621-T-G

183262012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48320363-A-T

183262662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48319888-G-A

183262662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 48319888-G-T

http://identifiers.org/hco/4/GRCh38#183263098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48319575-C-A

183263098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319575-C-G

183263104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319569-A-G

183263147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319531-G-C

183263178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319489-A-G

183263242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319423-C-G

183263307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319359-G-A

183263420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319280-C-T

183263425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319275-T-C

183263746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48319121-G-A

183263963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48318997-T-C

http://identifiers.org/hco/4/GRCh38#183264063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48318896-C-A

183264319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48318654-A-T

183264427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48318544-A-G

183264516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48318425-G-C

183264939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317703-A-G

http://identifiers.org/hco/4/GRCh38#183264961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48317684-C-A

http://identifiers.org/hco/4/GRCh38#183264965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48317680-C-A

183264965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317680-C-T

183265182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317497-G-C

183265182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317497-G-T

183265184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317495-A-G

http://identifiers.org/hco/4/GRCh38#183265185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48317494-C-A

183265196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317483-A-G

183265442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317331-G-C

183265551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317248-T-C

183265563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317236-C-T

http://identifiers.org/hco/4/GRCh38#183265564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48317235-A-C

183265619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317223-G-T

183265795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317052-A-G

183265803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48317044-C-T

183265929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48316908-T-C

http://identifiers.org/hco/4/GRCh38#183265973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48316862-C-A

183265973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48316862-C-T

183266003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48316837-A-G

183266325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48316299-A-G

183266466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48316193-A-G

183266834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315998-A-G

183266862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315973-G-A

183266888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315938-T-A

183267147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315664-G-A

183267160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315650-A-G

183267180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315633-G-C

183267182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315631-C-G

183267281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48315537-C-G

183268027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312846-A-G

183268108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312780-T-A

183268200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312674-G-T

http://identifiers.org/hco/4/GRCh38#183268218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48312661-A-C

183268219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312660-G-A

183268293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312586-T-C

183268298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312581-T-C

183268321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312565-T-C

183268549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312345-T-G

183268653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312251-A-G

183268653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312251-A-T

183268678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312237-G-A

183268678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312237-G-C

183268678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312237-G-T

183268692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312223-T-C

183268755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312164-G-C

183268769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312151-C-T

183268865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312062-T-C

183268865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312062-T-G

http://identifiers.org/hco/4/GRCh38#183268866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48312061-C-A

183268919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312007-T-C

http://identifiers.org/hco/4/GRCh38#183268920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48312006-C-A

183268920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48312006-C-T

183268941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311985-T-C

183268941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311985-T-G

183268959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311967-T-C

http://identifiers.org/hco/4/GRCh38#183268985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48311941-C-A

183269081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48311845-C-T

183269119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 48311807-G-A

183269119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 48311807-G-T

http://identifiers.org/hco/4/GRCh38#183269189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48311732-C-A

183269189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311732-C-G

183269189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311732-C-T

183269192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311729-A-G

183269391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311386-G-A

183269391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48311386-G-T

http://identifiers.org/hco/4/GRCh38#183269445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48311331-C-A

183269708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48310886-A-G

http://identifiers.org/hco/4/GRCh38#183269753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48310844-C-A

http://identifiers.org/hco/4/GRCh38#183269843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48310785-A-C

183269843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48310785-A-G

183269850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48310778-T-A

183270168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48310482-G-A

183270168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48310482-G-C

183270350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48310301-G-C

http://identifiers.org/hco/4/GRCh38#183270954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48309515-A-C

183270954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309515-A-G

http://identifiers.org/hco/4/GRCh38#183270981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48309487-C-A

183270982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309486-T-A

183270982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309486-T-C

183270989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309479-A-G

http://identifiers.org/hco/4/GRCh38#183271037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48309428-C-A

183271037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309428-C-T

http://identifiers.org/hco/4/GRCh38#183271043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48309419-C-A

183271043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48309419-C-T

183271185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 48309276-G-T

183271224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48309234-G-A

183271274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48309190-A-G

183271274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48309190-A-T

183271292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48309180-A-T

183271379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48309125-T-G

183271403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48309099-C-T

183271569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48308980-T-C

183279871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305911-C-T

183280029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305745-T-C

183280029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305745-T-G

183280052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305722-A-G

183280140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305634-A-G

183280141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305633-T-C

183280224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305555-C-T

183280467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305355-A-G

183280496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305327-C-G

183280496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305327-C-T

183280515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305308-C-T

183280599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305222-A-G

183280625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305196-T-A

183280625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 48305196-T-G

http://identifiers.org/hco/4/GRCh38#183280645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48305176-C-A

183280842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48304993-C-G

183280842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 48304993-C-T

183280873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48304962-A-T

http://identifiers.org/hco/4/GRCh38#183280875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48304960-C-A

183281008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304827-G-A

183281008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304827-G-T

183281014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304821-T-C

183281014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304821-T-G

183281031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304807-G-T

183281056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304783-G-A

183281099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304742-T-G

http://identifiers.org/hco/4/GRCh38#183281103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48304738-C-A

183281103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304738-C-T

183281194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304651-T-C

183281329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304361-C-G

183281329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304361-C-T

183281350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48304341-G-A

http://identifiers.org/hco/4/GRCh38#183281451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48304169-C-A

183281451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48304169-C-T

183281549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48304067-G-A

183281812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48303854-T-A

183282066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48303625-C-T

183282275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302937-G-A

183282375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302840-T-A

183282460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302759-G-A

183282460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302759-G-T

http://identifiers.org/hco/4/GRCh38#183282521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48302705-A-C

183282541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302695-G-T

http://identifiers.org/hco/4/GRCh38#183282561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48302675-C-A

183282561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302675-C-T

http://identifiers.org/hco/4/GRCh38#183282677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48302556-C-A

183282677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 48302556-C-T

183282687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 48302543-T-C

183282724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48302506-G-A

183282724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48302506-G-C

183282724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 48302506-G-T

183282798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48302432-T-C

183282801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48302429-A-G

http://identifiers.org/hco/4/GRCh38#183282999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48302265-C-A

183283065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302203-T-A

183283075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302193-T-C

183283086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48302183-A-T

183284226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 48300591-G-A

183284306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 48300511-T-C

http://identifiers.org/hco/4/GRCh38#183284370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48300447-C-A

183284370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48300447-C-T

183284427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48300390-G-A

183284495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48300332-G-A

183284495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48300332-G-T

183284933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299965-T-C

183285094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299834-A-G

183285256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299730-T-G

183285267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299723-G-A

183285368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299674-T-C

183285392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299650-A-G

183285849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299396-A-G

183285864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299378-A-G

183285864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299378-A-T

183285869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299373-T-C

183285870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299372-G-T

http://identifiers.org/hco/4/GRCh38#183285872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48299370-C-A

183285874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299368-A-G

183285874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299368-A-T

http://identifiers.org/hco/4/GRCh38#183285875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48299367-C-A

183285875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299367-C-T

183285885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299357-T-C

183285885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299357-T-G

183285890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299352-A-T

183285915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299328-T-C

183286119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299153-G-A

183286119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299153-G-T

183286145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299131-T-C

183286145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299131-T-G

http://identifiers.org/hco/4/GRCh38#183286157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48299119-C-A

183286157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299119-C-T

http://identifiers.org/hco/4/GRCh38#183286159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48299117-C-A

183286159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299117-C-G

http://identifiers.org/hco/4/GRCh38#183286172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48299104-C-A

183286172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48299104-C-G

183286527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298749-G-T

183287556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298586-A-T

183287749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298420-A-G

183287764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298406-T-C

183287798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298374-C-T

183287813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298361-G-A

183287818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298356-T-C

183287922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298269-C-T

183287988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48298205-G-A

183288985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296491-C-T

http://identifiers.org/hco/4/GRCh38#183289080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48296391-A-C

183289102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296373-T-C

183289102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296373-T-G

183289151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296325-C-G

183289195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296281-T-A

183289281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296209-G-C

183289281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296209-G-T

http://identifiers.org/hco/4/GRCh38#183289308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48296199-C-A

183289308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296199-C-G

183289308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296199-C-T

http://identifiers.org/hco/4/GRCh38#183289312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48296195-C-A

183289312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48296195-C-T

183289444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48296089-A-G

183289444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48296089-A-T

183289465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48296068-G-A

183289465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48296068-G-T

183289564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48295969-G-A

183289594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48295939-G-A

183289594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 48295939-G-T

183289644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48295889-C-G

183289644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48295889-C-T

183289698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48295822-A-G

http://identifiers.org/hco/4/GRCh38#183290750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48294588-C-A

183292571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48293745-G-A

183295826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48288370-C-T

183295935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48288276-C-G

183296237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48288004-A-G

183296306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48287935-T-C

183299258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48287122-C-G

183299258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48287122-C-T

183299368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48287015-C-T

183299433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286952-A-G

183299706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286692-C-T

183299972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286502-G-A

183300071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286415-G-C

183300088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286398-G-A

183300190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286304-A-G

183300334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48286203-G-A

183312023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48285050-C-G

183312024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48285049-A-T

183312175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48284874-C-T

183312176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48284873-A-G

183312301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48284788-G-T

183312505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48284617-C-T

183312510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48284612-G-A

183315290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48282261-G-A

183315315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48282237-G-T

183315584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48281893-G-A

http://identifiers.org/hco/4/GRCh38#183315629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48281849-A-C

183315629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48281849-A-G

183315629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48281849-A-T

183315644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 48281834-T-C

183316050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281394-T-A

183316050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281394-T-C

183316050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281394-T-G

183316117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281357-G-T

183316238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281279-G-A

183316441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281118-G-T

183316445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48281114-G-T

183316647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280964-A-G

183316683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280932-G-A

183316683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280932-G-T

183316729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280888-G-T

183316813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280791-A-G

183316818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280786-G-C

183316900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280735-T-A

183317368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280231-T-C

183317382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48280217-G-T

183318387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48279251-T-A

183318405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48279233-T-A

183318426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48279212-T-C

183318456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 48279180-C-T

183318770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278907-G-T

183318773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278904-C-G

183318824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278853-T-A

183318824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278853-T-C

http://identifiers.org/hco/4/GRCh38#183318830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48278847-C-A

183318830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278847-C-T

183318831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278846-A-G

183318879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278815-G-T

183318909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278785-A-G

183318909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278785-A-T

183318923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278774-A-G

183319001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278719-G-A

183319010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278710-G-T

183319012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278708-A-G

183319067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278677-A-G

183319076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278669-T-G

183319077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278668-G-A

183319077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278668-G-T

183319239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278521-T-C

183319274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278502-T-C

183319274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278502-T-G

183319303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278465-T-C

183319478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278288-A-G

183319485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278281-G-T

183319506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48278262-C-T

183319587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48278193-A-G

183319606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 48278174-G-A

183319606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48278174-G-C

183319651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48278129-T-C

183319651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48278129-T-G

http://identifiers.org/hco/4/GRCh38#183319686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48278094-A-C

183319781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277999-C-G

183319781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 48277999-C-T

183319782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277998-T-C

183319830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277950-C-T

183319846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 48277934-G-A

183319846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277934-G-C

183319899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277881-A-G

183319899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 48277881-A-T

183320335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277451-T-A

183320335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277451-T-G

183320453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277335-T-A

183320506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277276-G-A

183320506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277276-G-T

183320517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277267-C-T

183320623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277150-C-T

183320625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277148-T-A

183320625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277148-T-C

183320626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277147-G-T

183320631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277142-G-A

183320631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277142-G-T

183320645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277128-G-A

183320645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277128-G-T

183320694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277076-T-A

183320694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277076-T-C

183320710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277060-A-G

183320710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: 48277060-A-T

http://identifiers.org/hco/4/GRCh38#183320740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24148
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#48277026-A-C