155923560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3 prime UTR variant
orthologous variants: 81863724-A-G

155923591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3 prime UTR variant
orthologous variants: 81863694-C-T

155923782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3 prime UTR variant
orthologous variants: 81863215-A-T

155924142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862846-T-A

155924235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862756-G-C

http://identifiers.org/hco/4/GRCh38#155924236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81862755-A-C

155924398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862599-T-A

155925173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862419-G-A

http://identifiers.org/hco/4/GRCh38#155925223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81862362-A-C

155925310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862307-T-G

155925387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862233-T-C

155925394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862226-G-T

155925436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862165-G-A

155925446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862155-T-C

http://identifiers.org/hco/4/GRCh38#155925461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81862140-C-A

155925470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862131-G-C

http://identifiers.org/hco/4/GRCh38#155925522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81862080-C-A

155925522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862080-C-T

155925550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81862061-C-T

http://identifiers.org/hco/4/GRCh38#155925566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81862052-C-A

155925643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861978-A-G

155925660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861960-T-C

155925795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861823-A-G

155925834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861783-T-C

155925864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861754-A-G

155925994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861615-A-G

155925995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861614-A-G

155926026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861583-G-A

155926026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81861583-G-T

155926052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81861549-G-A

155926052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81861549-G-T

155926063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 81861538-T-C

http://identifiers.org/hco/4/GRCh38#155926081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81861520-A-C

155926081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861520-A-G

155926164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861433-G-A

155926164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861433-G-C

155926164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861433-G-T

155926167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861430-T-C

155926185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861411-T-C

155926203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861399-G-T

155926235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861367-T-C

155926243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861359-G-T

155926555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861104-C-G

155926562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861097-C-T

155926636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81861024-C-T

http://identifiers.org/hco/4/GRCh38#155926743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81860915-A-C

155926798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81860879-G-C

http://identifiers.org/hco/4/GRCh38#155926932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81860749-C-A

155927001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81860684-C-T

http://identifiers.org/hco/4/GRCh38#155927207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81860501-C-A

155927269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81860437-T-C

155927347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81860360-T-G

155928056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859877-G-A

http://identifiers.org/hco/4/GRCh38#155928163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81859782-C-A

http://identifiers.org/hco/4/GRCh38#155928197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81859754-A-C

155928197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859754-A-G

155928197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859754-A-T

http://identifiers.org/hco/4/GRCh38#155928228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81859723-A-C

155928228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859723-A-G

155928228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859723-A-T

155928259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859670-T-A

155928259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 81859670-T-C

155928359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 81859573-A-G

155928386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 81859546-G-A

155928386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 81859546-G-C

155928419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 81859513-G-A

155929571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81858812-G-T

155929762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858617-A-G

155929786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858594-T-C

155929866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858515-A-G

155929909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858472-T-C

http://identifiers.org/hco/4/GRCh38#155929957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81858430-A-C

155930111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858292-C-T

http://identifiers.org/hco/4/GRCh38#155930121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81858282-A-C

155930213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81858181-G-A

155930635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857776-G-A

155930652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857760-T-A

155930723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857704-T-G

155930809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857623-C-T

155930923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857525-T-C

155931069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857385-G-C

155931180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857246-G-A

155931372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857082-G-A

155931415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81857043-C-T

http://identifiers.org/hco/4/GRCh38#155931908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81856699-A-C

155931930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856678-G-A

155931977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856640-T-C

155932087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856531-T-A

155932449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856152-T-A

155932465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81856136-G-C

http://identifiers.org/hco/4/GRCh38#155932493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81856112-C-A

http://identifiers.org/hco/4/GRCh38#155932751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81855888-C-A

155932751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855888-C-T

155932773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855867-T-C

155932776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855864-C-G

155932785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855855-C-T

http://identifiers.org/hco/4/GRCh38#155932801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81855843-C-A

155932832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855812-C-T

155932988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855685-G-C

http://identifiers.org/hco/4/GRCh38#155935404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81855566-A-C

155935522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855473-T-C

155935731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855264-T-C

155935878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855104-A-G

155935918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855070-T-A

155935926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81855062-A-G

155936191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854840-C-T

155936385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854678-T-C

155936745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854334-G-A

155936755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854324-A-G

155936841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854239-T-C

155936887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854193-G-C

155937037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81854017-T-A

155937103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853991-A-G

155937177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853934-T-C

155937532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853573-A-G

155938016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853308-T-C

155938074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853247-T-C

155938169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853166-C-T

155938224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81853128-C-T

http://identifiers.org/hco/4/GRCh38#155938503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81852880-C-A

155938503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852880-C-T

155939116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852661-A-G

155939201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852576-A-T

http://identifiers.org/hco/4/GRCh38#155939220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81852467-A-C

155939220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852467-A-G

155939220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852467-A-T

155939297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852398-T-C

155939297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852398-T-G

155939361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852343-G-A

155939361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852343-G-T

155939465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81852240-T-C

155939630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81852059-G-A

155941163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850669-G-A

155941536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850333-T-C

http://identifiers.org/hco/4/GRCh38#155941623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81850238-C-A

155941623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850238-C-T

155941624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850237-A-G

155941675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850191-A-G

155941799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850078-A-T

155941815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81850059-G-A

155941984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849912-T-C

http://identifiers.org/hco/4/GRCh38#155942166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849770-C-A

http://identifiers.org/hco/4/GRCh38#155942167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849769-C-A

155942167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849769-C-T

http://identifiers.org/hco/4/GRCh38#155942177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849759-C-A

155942177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849759-C-G

155942186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849752-G-A

155942186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849752-G-T

155942201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849741-C-T

155942208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849734-G-A

155942208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849734-G-T

155942238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849712-T-C

155942238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849712-T-G

155942245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849705-T-C

155942252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849700-A-G

155942261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849691-T-C

155942433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 81849521-A-G

155942465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849489-A-G

155942584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849458-T-C

http://identifiers.org/hco/4/GRCh38#155942588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849455-A-C

155943051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849043-G-A

http://identifiers.org/hco/4/GRCh38#155943064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849030-C-A

155943064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849030-C-T

http://identifiers.org/hco/4/GRCh38#155943095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81849001-C-A

155943095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81849001-C-T

155943138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848960-A-G

155943139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848959-G-T

155943178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 81848920-A-G

155943257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 81848844-A-G

155943492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848697-C-T

http://identifiers.org/hco/4/GRCh38#155943733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81848502-A-C

155943942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848309-G-A

155943942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848309-G-T

155943945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848306-T-C

155944063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81848202-T-G

155944509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847748-G-A

155945280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847282-A-T

155945470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81847123-A-G

155947197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81846179-T-G

155947215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81846161-C-T

155947381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81846047-T-A

http://identifiers.org/hco/4/GRCh38#155947406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81846029-A-C

155947724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845718-C-T

155947731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845711-T-C

155947778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845668-G-A

http://identifiers.org/hco/4/GRCh38#155947955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81845457-C-A

155947955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845457-C-G

155948131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845272-T-C

155948338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81845070-A-G

155948352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844991-T-C

155948669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844586-T-A

155948821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844437-T-C

155948982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844299-G-T

155949124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844171-T-C

155949252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81844040-T-C

155949385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843897-G-C

155949401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843881-T-C

155949430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843852-G-A

155949430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843852-G-T

155949596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843599-T-C

155949764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843448-G-A

http://identifiers.org/hco/4/GRCh38#155949811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81843401-A-C

155950234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843320-T-C

155950239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843315-T-C

http://identifiers.org/hco/4/GRCh38#155950366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81843128-C-A

155950409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81843089-G-A

155952499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81841009-G-A

155952557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81840973-G-C

155952891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81840630-T-C

http://identifiers.org/hco/4/GRCh38#155953112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81840435-A-C

155953521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81840146-G-A

155953574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81840133-G-A

155953574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 81840133-G-T

155953665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81840102-G-A

155953665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 81840102-G-T

155953720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 81840073-G-A

155953720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 81840073-G-T

http://identifiers.org/hco/4/GRCh38#155953731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81840062-A-C

155953731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 81840062-A-G

155953731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 81840062-A-T

http://identifiers.org/hco/4/GRCh38#155953795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#81840027-C-A

155953795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 81840027-C-G

155953795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 81840027-C-T

http://identifiers.org/hco/4/GRCh38#155953798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81840024-C-A

155953798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81840024-C-G

155953798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 81840024-C-T

http://identifiers.org/hco/4/GRCh38#155953803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81840019-C-A

155953803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 81840019-C-T

http://identifiers.org/hco/4/GRCh38#155953862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81839954-C-A

155953862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81839954-C-T

155953866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 81839950-T-C

155953876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 81839945-G-A

155953876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 81839945-G-C

155953876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 81839945-G-T

http://identifiers.org/hco/4/GRCh38#155953907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#81839914-C-A

155953907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2542
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 81839914-C-T