http://identifiers.org/hco/10/GRCh38#35332135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#9459139-C-A

35332135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9459139-C-T

35332136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9459138-G-A

35332254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459027-T-C

35332307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9458958-G-A

35332307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9458958-G-T

35333982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9451995-C-T

35334007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9451968-A-G

35334801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9450922-T-C

35334841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9450896-G-A

35334843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9450894-T-C

http://identifiers.org/hco/10/GRCh38#35334846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9450891-C-A

35334873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9450868-T-C

http://identifiers.org/hco/10/GRCh38#35336431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9450263-C-A

http://identifiers.org/hco/10/GRCh38#35336455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9450231-C-A

35336455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9450231-C-T

http://identifiers.org/hco/10/GRCh38#35336564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#9450127-C-A

35336564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9450127-C-G

http://identifiers.org/hco/10/GRCh38#35336964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#9449716-C-A

35336964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9449716-C-G

35336964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 9449716-C-T

35337201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9449522-A-G

35337201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9449522-A-T

35337302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9449467-G-A

35337302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9449467-G-C

35337302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9449467-G-T

35337354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9449425-G-A

35337354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9449425-G-C

35338125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9448704-C-T

35339105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444723-A-G

http://identifiers.org/hco/10/GRCh38#35339202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9444612-C-A

35346270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9441851-C-T

35353684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439163-C-G

35353689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439158-C-T

35354078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9438838-G-C

35354968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9438024-T-C

35360150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435978-T-C

35432842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9404711-C-T

35440409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400975-C-G

35440412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400972-C-T

35440503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400883-G-A

35440723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400681-G-A

35440740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400670-A-G

35441359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400050-A-G

35441385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400020-A-G

35451163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395767-C-T

35451370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395563-A-G

35451546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395384-T-G

35452096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394879-T-G

35452257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394781-G-A

35452455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394595-A-G

35452489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394566-A-G

35452526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394536-G-A

35456277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393233-G-C

35456593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392955-C-T

35456722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392821-G-T

http://identifiers.org/hco/10/GRCh38#35457001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9392545-C-A

http://identifiers.org/hco/10/GRCh38#35457013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9392533-C-A

35457013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392533-C-G

35457133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392407-A-G

35457253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392319-C-T

35457325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392247-G-A

35458000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391065-C-G

35458000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391065-C-T

35481080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9389091-G-A

35481295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388974-C-T

35481495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388835-T-C

35481603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388758-G-T

35482556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387509-A-G

35483032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387155-A-G

35483032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387155-A-T

http://identifiers.org/hco/10/GRCh38#35483092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9387109-A-C

35483280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386913-G-A

http://identifiers.org/hco/10/GRCh38#35483285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9386911-A-C

35483285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386911-A-T

35483327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386888-A-G

35483368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386850-G-C

35483368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386850-G-T

35483602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386623-T-C

35483602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386623-T-G

35483921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386304-A-G

35483950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9386248-C-T

35484289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9385931-G-C

35484762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9385583-A-G

35484861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9385511-G-T

35484928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9385442-T-G

35492965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383335-C-G

35492965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383335-C-T

35493034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383253-C-T

http://identifiers.org/hco/10/GRCh38#35493209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9383092-C-A

35493209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383092-C-T

35493212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383089-A-G

35493300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383002-C-G

35493300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9383002-C-T

35493310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382993-G-T

35493389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382916-T-C

35493526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382822-C-T

35493577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382776-A-G

35493675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382614-C-G

35493926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382175-A-G

35493993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382118-C-T

35494006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382105-G-A

35494031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382081-G-C

35494092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382023-T-C

http://identifiers.org/hco/10/GRCh38#35494222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9382008-C-A

35494222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382008-C-G

35494222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382008-C-T

35494492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381824-A-G

http://identifiers.org/hco/10/GRCh38#35495175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9381380-C-A

35495175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381380-C-T

35495275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381268-T-C

35495705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9380955-G-A

35495705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9380955-G-C

35500743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9378366-G-C

35500993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9378163-A-G

35501254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9378050-T-C

35501458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9377871-A-T

35501716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9377648-G-A

35501716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9377648-G-C

35502866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376613-C-T

35504250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374723-G-A

35504341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9374653-C-T

35504530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374531-G-C

http://identifiers.org/hco/10/GRCh38#35504546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9374515-A-C

35504546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374515-A-G

35505115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374289-G-A

35505165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374243-C-G

http://identifiers.org/hco/10/GRCh38#35505245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9374187-C-A

35505253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374179-G-T

35505283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9374137-A-T

35505517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9373942-A-G

35505681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9373798-G-A

35505703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9373776-G-A

35505839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9373609-T-C

35513042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9369930-T-C

35513128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9369850-C-G

35515031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355354-T-C

35515371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355047-T-C

35516490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353529-A-G

35516490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353529-A-T

35516537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9353491-A-G

35516625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 9353403-T-C

35516625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 9353403-T-G

35516655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353332-T-A

35516655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353332-T-C

35516655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9353332-T-G

35517239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352390-C-T

35517338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9352284-G-A

35517846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9351846-G-T

35518001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9351706-G-A

35524205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9351173-A-G

35524245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9351133-T-A

35524872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9350646-T-C

35525435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349889-A-G

35525496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349830-G-A

35525496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349830-G-C

35525536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349790-T-A

35525536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349790-T-C

http://identifiers.org/hco/10/GRCh38#35525733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9349613-A-C

35525823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349541-T-C

35525823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349541-T-G

35525859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349505-G-T

35526022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349359-A-G

http://identifiers.org/hco/10/GRCh38#35526106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9349299-C-A

35526106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349299-C-T

35526137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9349272-A-G

35527554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9347516-A-G

35529992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9345450-C-T

35530051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9345383-C-G

http://identifiers.org/hco/10/GRCh38#35530340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9345167-C-A

35530340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9345167-C-T

35531181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9344711-A-G

35531203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9344689-A-T

35546293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9340170-C-T

35546418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9340043-G-A

35546581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339916-C-G

35546772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339728-C-T

35547166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339392-C-G

35547229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339351-T-C

35547324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339266-T-C

35547394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9339206-C-T

http://identifiers.org/hco/10/GRCh38#35550802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9338039-C-A

http://identifiers.org/hco/10/GRCh38#35552916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9333036-C-A

35552916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9333036-C-T

35556288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331255-G-T

35556377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331138-C-G

35556377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331138-C-T

35556499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9331032-T-C

35556630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330911-G-T

35556800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330826-C-T

http://identifiers.org/hco/10/GRCh38#35557315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9330491-C-A

35557387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330420-T-G

35557775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9330249-T-C

35558249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329864-G-A

35558285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329829-G-A

35558324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329809-C-T

35558332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329801-T-G

35558575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329541-A-G

35558645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329471-C-G

35558705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329409-C-T

35558798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329331-G-T

35558859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329276-G-A

35558953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9329174-G-A

35565867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319710-A-T

http://identifiers.org/hco/10/GRCh38#35565915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319663-C-A

http://identifiers.org/hco/10/GRCh38#35565916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319662-C-A

35565916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319662-C-T

http://identifiers.org/hco/10/GRCh38#35565926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319652-C-A

35565926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319652-C-T

35565977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9319613-C-G

35566153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9319439-C-G

35566153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9319439-C-T

http://identifiers.org/hco/10/GRCh38#35566237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319358-C-A

35566237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9319358-C-T

http://identifiers.org/hco/10/GRCh38#35566277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319334-C-A

35566277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9319334-C-G

35566277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9319334-C-T

http://identifiers.org/hco/10/GRCh38#35566279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9319332-C-A

35566279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9319332-C-G

35566279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9319332-C-T

35567018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9319196-A-G

35567091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9319120-C-T

35567162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9319065-A-T

35567325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9318913-G-A

35567361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: intron variant
orthologous variants: 9318893-C-G

35569169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: undefined
orthologous variants: 9316555-A-G

35569242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316483-T-A

35569242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316483-T-C

35569292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316430-G-A

35569292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316430-G-T

http://identifiers.org/hco/10/GRCh38#35569322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9316383-C-A

http://identifiers.org/hco/10/GRCh38#35569357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9316344-C-A

http://identifiers.org/hco/10/GRCh38#35569418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9316281-C-A

35569418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316281-C-T

35569465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316238-A-G

35569650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9316025-T-C

35569875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9315797-C-G

http://identifiers.org/hco/10/GRCh38#35570056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9315567-C-A

35570056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9315567-C-T

http://identifiers.org/hco/10/GRCh38#35570103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#9315525-C-A

35570106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9315522-G-A

35570106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9315522-G-T

35570403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9315233-G-T

35570812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9314852-C-T

35571037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9314667-A-G

35571124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9314580-C-T

35571199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9314511-T-C

35572157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9313632-G-T

35572255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23354
most severe consequence: 3 prime UTR variant
orthologous variants: 9313515-C-T